Professional Documents
Culture Documents
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In partial fulfillment of the requirements
for the degree of
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(2009-2011)
Of
Punjab Technical University
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Kharar ± 140301, Distt. Mohali (PB.)
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r ital to every operation is co-operation´. We all agree to this quotation put forth by
Mr. Frank Tyger. This project was successful due to the co -operation extended by
people who have truly contributed towards it.
I thank + ,- for bestowing upon me his choicest blessings and run ning all the
things in the right direction.
First of all I would like to convey my thanks to Mr. Z.S. Dhaliwal (Internal Guide,
Faculty CMTR) for his constant suggestions which have resulted in successful
completion of project. It is a great privilege for me to express my sincere gratitude to
my reverend project guide Mr. Narendera Kumar Tripathi (A ccounts Dpt. & H.R.O.)
for his valuable guidance and overall help throughout the training period.
I am immensely thankful to Mr. Inderjeet Singh & Mr. Sanjay Gupta (H.R.O.) for his
their support and kind help which I get for the completion of this project .
ABHISHEK THAKUR
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c
c/ which are
followed in c, Paonta Sahib (H.P.).
So the choice of the Performance Appraisal Practices as my project was obvious for
the partial completion of my specialization in rMBA (HR)´.
During the course of my project I have gathered certain information, which has led to
some constructive facts in the areas of the company.
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Employee development is the successful function of any company. If the employee
are skilled, capable and fit for the job they are expected to do; they will be satisfied
there will be minimum number of square pegs in the round hole of any company.
Ranbaxy Labs Ltd. is trying to make all the people working in the organization more
skilled and capable so that it may improve its products in terms of quality and
quantity and can build a mark upon its competitors.
In order to measure the capability of employee
$
#+ is done. It
aims to measure the ability as well as weaknesses of an employee. A feedback is
given to every employee after hi/her performance is measured. This helps him to
know about his/her strengths and weakn esses. This also helps the management to
provide proper training to employees to upgrade their skills and performance.
Performance Appraisal is the base of promotions, increments, training and
development etc.
"#-$
,
+#
The earliest drugstores date back to the middle Ages. The first known drugstore was
opened by Arabian pharmacists in Baghdad in 754, and many more soon began
operating throughout the medieval Islamic world and eventually medieval Europe. By
the 19th century, many of the drug stores in Europe and North America had
eventually developed into larger pharmaceutical companies.
Most of today's major pharmaceutical companies were founded in the late 19th and
early 20th centuries. Key discoveries of the 1920s and 1930s, such as insulin and
penicillin, became mass-manufactured and distributed. Switzerlan d, Germany and
Italy had particularly strong industries, with the UK, US, Belgium and the Netherlands
following suit.
Legislation was enacted to test and approve drugs and to require appropriate
labelling. Prescription and non -prescription drugs became legally distinguished from
one another as the pharmaceutical industry matured. The industry got underway in
earnest from the 1950s, due to the development of systematic scientific approaches,
understanding of human biology (including DNA) and sophisticated manufacturing
techniques.
Numerous new drugs were developed during the 1950s and mass -produced and
marketed through the 1960s. These included the first oral contraceptive, "The Pill",
Cortisone, blood-pressure drugs and other heart medications. MAO Inhibitors,
chlorpromazine (Thorazine), Haldol (Haloperidol) and the tranquilizers ushered in the
age of psychiatric medication. alium (diazepam), discovered in 1960, was marketed
from 1963 and rapidly became the most prescribed drug in history, prior to
controversy over dependency and habituation.
Attempts were made to increase regulation and to limit financial links between
companies and prescribing physicians, including by the relatively new U.S. Food and
Drug Administration (FDA). Such calls increased in the 1960s after the thalidomide
tragedy came to light, in which the use of a new tranquilizer in pregnant women
caused severe birth defects. In 1964, the World Medical Association issued its
Declaration of Helsinki, which set standards for clinical research and demanded that
subjects give their informed consent before enrolling in an experiment.
Pharmaceutical companies became required to prove efficacy in clinical trials before
marketing drugs.
Cancer drugs were a feature of the 1970s. From 1978, India took over as the primary
centre of pharmaceutical production without patent protection.
The industry remained relatively small scale until the 1970s when it began to expand
at a greater rate. Legislation allowing for strong patents, to cover both the process of
manufacture and the specific products came in to force in most countries. By the
mid-1980s, small biotechnology firms were struggling for survival, which led to the
formation of mutually beneficial partnerships with large pharmaceutical companies
and a host of corporate buyouts of the smaller firms. Pharmaceutical manufacturing
became concentrated, with a few large companies holding a dominant position
throughout the world and with a few companies producing medicines within each
country.
The pharmaceutical industry entered the 1980s pressured by economics and a host
of new regulations, b oth safety and environmental, but also transformed by new DNA
chemistries and new technologies for analysis and computation. Drugs for heart
disease and for AIDS were a feature of the 1980s, involving challenges to regulatory
bodies and a faster approval p rocess.
Managed care and Health maintenance organizations (HMOs) spread during the
1980s as part of an effort to contain rising medical costs, and the development of
preventative and maintenance medications became more important. A new business
atmosphere became institutionalized in the 1990s, characterized by mergers and
takeovers, and by a dramatic increase in the use of contract research organizations
for clinical development and even for basic R&D. The pharmaceutical industry
confronted a new business climate and new regulations, born in part from dealing
with world market forces and protests by activists in developing countries. Animal
Rights activism was also a challenge.
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The Indian Pharmaceutical Industry today is in the front rank of India¶s science -
based industries with wide ranging capabilities in the complex field of drug
manufacture and technology. A highly organized sector, the Indian Pharma Industry
is estimated to be worth $ 4.5 billion, growing at about 8 to 9 percent annually. It
ranks very high in the third world, in terms of technology, quality and range of
medicines manufactured. From simple headache pills to sophisticated antibiotics and
complex cardiac compounds, almost every type of medicine is now made
indigenously.
Playing a key role in promoting and sustaining development in the vital field of
medicines, Indian Pharma Industry boasts of quality producers and many units
approved by regulatory authorities in USA and UK. International companies
associated with this sector have stimulated, assisted and spearheaded this dynamic
development in the past 53 years and helped to put India on the ph armaceutical map
of the world.
The Indian Pharmaceutical sector is highly fragmented with more than 20,000
registered units. It has expanded drastically in the last two decades. The leading 250
pharmaceutical companies control 70% of the market with mark et leader holding
nearly 7% of the market share. It is an extremely fragmented market with severe
price competition and government price control .
The pharmaceutical industry in India meets around 70% of the country's demand for
bulk drugs, drug intermediates, pharmaceutical formulations, chemicals, tablets,
capsules, orals and injectibles. There are about 250 large units and about 8000
Small Scale Units, which form the core of the pharmaceutical industry in India
(including 5 Central Public Sector Units). These units produce the complete range of
pharmaceutical formulations, i.e., medicines ready for consumption by patients and
about 350 bulk drugs, i.e., chemicals having therapeutic value and used for
production of pharmaceutical formulations.
1
º 23$
4 India has a pool of personnel with high managerial and
technical competence as also skilled workforce. It has an educated work force
and English is commonly used. Professional services are easily available.
º +)
+234 India has a 64 year old democracy and hence
has a solid legal framework and strong financial markets. There is already an
established international industry and business co mmunity.
The Indian pharmaceutical industry grew at a very slow pace from 1947 to 1970,
largely due to the lack of incentives and the failure of the government to set -up a
concrete regulatory framework.
The introduction of the IPA - which did not recognize product patents but only
process patents - provided a major thrust to the industry and its companies, which,
through the process of reverse -engineering, began to produce bulk drugs and
formulations at lower costs. This led to high fragmentation in the industry, due to the
emergence of a number of small firms.
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There are several national and international pharmaceutical companies that operate
in India. Most of the country's requirements for pharmaceutical products are met by
these companies. Some of them are briefly described below:
º -7# # manufactures and markets a wide range of
pharmaceuticals both in India and abroad. The company has 60 active
pharmaceutical ingredients to manufacture drugs, critical care products,
diagnostic kits and biotechnology products. The company has 6 FDA plants
that produce active pharma ingredients and 7 FDA inspected and ISO 9001
and ISO 14001 certified plants. Dr. Reddy's Q1 FY10 result shows the
revenues of the company at Rs. 18,189 million which is up by 21%. During
this quarter the company introduced 24 new gene ric products, applied for 22
new generic product registrations and filed 4 DMFs.
º
,+#
+ is the second largest pharmaceutical healthcare company
in India. The brands manufactured by the company include Gardenal, Ismo,
Stemetil, Rejoint, Supradyn, Phensedyl and Haemaccel. Nicholas Piramal has
entered into join ventures and alliances with sever al international corporations
like Cheissi, Italy; I AX Corp; UK, F. Hoffmann -La Roche Ltd., Allergan Inc.,
USA etc.
º (+0 c,3+ %(c!& is a United Kingdom based pharma company; it is
the world's second largest pharmaceutical company. The company's portfolio
of pharma products consist of central nervous system, respiratory, oncology,
vaccines, anti-infectives and gastro-intestinal/metabolic products among
others. On November 2009, the FDA had announced that the H1N1 vaccine
manufactured by GSK would join the list of the four vaccines approved.
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With several companies slated to make investments in India, the future scenario of
the pharmaceutical industry in looks pretty promising. The country's pharmaceutical
industry has tremendous potential of growth considering all the projects that are in
the pipeline. Some of the future initiatives are:
º According to a study by FICCI-Ernst & Young India will open a probable US$
8 billion market for MNCs selling expensive drugs by 2015.
º The study also says that the domestic pharma market is likely to reach US$
20 billion by 2015.
º The Minister of Commerce estimates that US$ 6.31 billion will be invested in
the domestic pharmaceutical sector.
º Public spending on healthcare is likely to raise from 7 per cent of GDP in 2007
to 13 per cent of GDP by 2015.
º Dr Reddy's Laboratories has tied up with GlaxoSmithKline to develop and
market generics and formulations in upcoming markets overseas.
º Lupin, a Mumbai based pharmaceutical company is looking to tap
opportunities of about US$ 200 million in the US oral contraceptives m arket.
º Due to the low cost of R&D, the Indian pharmaceutical off -shoring industry is
designated to turn out to be a US$ 2.5 billion opportunity by 2012.
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To understand the implications of the environment on any industry it is imperative to
study the four cardinal influencers on the industry namely Political, Economic, Social
and Technological factors. It is rather unfortunate that in India these factors ha ve a
rather disproportionate influence on the functioning of a commercial organization.
From the days of independence the business environment has been overly regulated
by a handful of bureaucrats, middlemen, businessmen and politicians. Its only a
decade since the country has seen an emergence of a political thought that
encourages free enterprise. 2+
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1. Today there is political uncertainty in the air. A combination of diverse
political thought have got togethe r to cobble together a rag -tag coalition, that
is riddle with ideological contradictions. Therefore, any consistent political or
economic policy cannot be expected. This muddies the investment field.
2. The Minister in charge of the industry has been threatening to impose even
more stringent Price Control on the industry than before. This is throwing
many an investment plan into the doldrums.
3. DPCO which is the bible for the industry has in effect wo rked contrary to the
stated objectives. DPCO nullifies the market forces from encouraging
competitive pricing of goods dictated by the market. Now the pricing is
determined by the Government based on the approved costs irrespective of
the real costs.
4. Effective January, 2005 the country goes in for the IPR (Intellectual Property
Rights) regime, popularly known as the Patent Act. This Act will impact the
Pharmaceutical Industry the most. Thus far an Indian company could escape
paying a patent fee to the inventor of a drug by manufacturing it using a
different chemical route. Indian companies exploited this law and used the
reverse-engineering route to invent a lot of alternate manufacturing methods.
A lot of money was saved this way. This also encouraged competing
company to market their versions of the same drug. That meant that the
impurities and trace elements found in different brands of the same substance
were different both in qualification as well as in quantum.
Therefore different brands o f the same medicine were truly different. Here
Branding actually meant quality and a purer brand actually had purer active
ingredient and lesser or less toxic impurities.
Product patent regime will eliminate all this. Now, a patented drug would be
manufactured using the same chemical route and would be manufactured by
the inventor or his licentiates using the chemicals with same specifications.
Therefore, all the brands of the same active ingredient would not have any
difference in purity and impuritie s. The different brands would have to
compete on the basis of non input-related innovations such as packaging,
color, flavors, Excipients etc.
This is the biggest change the environment is going to impose on the industry.
The marketing effort would be now focused on logistics, communications, and
economy of operation, extra-ingredient innovations and of course pricing.
5. In Pharma industry there is a huge PSU segment which is chronically sick and
highly inefficient. The Government puts the surpluses generated by efficient
units into the price equalization account of inefficient units thereby unduly
subsidizing them. On a long term basis this has made practically everybody
inefficient.
6. Effective the January, 2005 the Government has shifted from charging the
Excise Duty on the cost of manufacturing to the MRP thereby making the
finished products more costly. Just for a few extra bucks the current
government has made many a life saving drugs unaffordable to the poor.
(11#
The government of India has undertaken several including policy initiatives and tax
breaks for the growth of the pharmaceutical business in India. Some of the measures
adopted are:
º Pharmaceutical units are eligible for weighted tax reduction at 150% for the
research and development expenditure obtained.
º Two new schemes namely, New Millennium Indian Technology Leadership
Initiative and the Drugs and Pharmaceuticals Research Program have been
launched by the Government.
º The Government is contemplating the creation of SR or special purpose
vehicles with an insurance cover to be used for funding new drug research.
º The Department of Pharmaceuticals is mulling the creation of drug research
facilities which can be used by private companies for research work on rent.
º
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º India spends a very small proportion of its GDP on healthcare (A mere 1%). This has
stunted the demand and therefore the growth of the industry.
º Per capita income of an average Indian is low (Rs. 12,890 ), therefore, spending on
the healthcare takes a low priority. An Indian would visit a doctor only when there is
an emergency. This has led to a mushrooming of unqualified doctors and spread of
non-standardized medication.
º The incidences of Taxes are very high. There is Excise Duty (State & Central),
Custom Duty, Service Tax, Profession Tax, License Fees, Royalty, Pollution
Clearance Tax, Hazardous substance (Storage & Handling) license, income tax,
Stamp Duty and a host of othe r levies and charges to be paid. On an average it
amounts to no less than 40 -45% of the costs.
º There are only 50, 00,000 Medical shop s. Again this affects adversely the
distribution of medicines and also adds to the distribution costs.
º India is a high interest rate regime. Therefore the cost of funds is double that in
America. This adds to the cost of goods.
º Adequate storage and tra nsportation facilities for special drugs are lacking. A study
had indicated that nearly 60% of the Retail Chemists do not have adequate
refrigeration facilities and store drugs under sub -optimal conditions. This affects the
quality of the drugs administe red and of course adds to the costs.
º India has poor roads and rail network. Therefore, the transportation time is higher.
This calls for higher inventory carrying costs and longer delivery time. All this adds to
the invisible costs. It¶s only during th e last couple of years that good quality highways
have been constructed.
,(2,c
India's US$ 3.1 billion pharmaceutical industry is growing at the rate of 14 percent
per year. It is one of the largest and most advanced among the developing countries.
The pharmaceutical industry in India is among the most highly organized sectors.
This industry plays an important role in promoting and sustaining development in the
field of global medicine. Due to the presence of low cost manufacturing facilities,
educated and skilled manpower and cheap labor forc e among others, the industry is
set to scale new heights in the fields of production, development, manufacturing and
research. In 2008, the domestic pharma market in India was expected to be US$
10.76 billion and this is likely to increase at a compound an nual growth rate of 9.9
per cent until 2010 and subsequently at 9.5 per cent till the year 2015.
,0#
In the recent years, despite the slowdown witnessed in the global economy, exports
from the pharmaceutical industry in India have shown good buoyancy in growth.
Export has become an important driving force for growth in this industry with more
than 50 % revenue coming from the overseas markets. For the financial year 2008 -
09 the export of drugs is estimated to be $8.25 billion as per the Pharma ceutical
Export Council of India, which is an organization, set up by the Government of India.
A survey undertaken by FICCI, the oldest industry chamber in India has predicted
16% growth in the export of India's pharmaceutical growth during 2009 -2010
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1. Poverty and associated malnutrition dramatically exacerbate the incidence of
Malaria and TB, preventable diseases that continue to play havoc in India
decades after they were eradicated in other countries.
2. Poor Sanitation and po lluted water sources prematurely end the life of about 1
million children under the age of five every year.
6. Smoking, gutka, drinking and poor oral hygiene is adding to the healthcare
problem.
9. Early child bearing affects the health standards of women and children.
10. Ignorance of inoculation and vaccination has prevented the eradication of
diseases like polio, chicken -pox, small-pox, mumps and measles.
11. People don¶t go in for vaccination due superstitious beliefs and any sort of
ailment is considered as a curse from God for sins committed.
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1. Advanced automated machines have increased the o utput and reduced the
cost.
Indian companies need to attain the right product -mix for sustained future growth.
Core competencies will play an important role in determining the future of many
Indian pharmaceutical companies in the post product -patent regime after 2005.
Indian companies, in an effort to consolidate their position, will have to increasingly
look at merger and acquisition options of either companies or products. This would
help them to offset loss of new product options, improve their R&D efforts and
improve distribution to penetrate mark ets.
Research and development has always taken the back seat amongst Indian
pharmaceutical companies. In order to stay competitive in the future , Indian
companies will have to refocus and invest heavily in R&D.
The Indian pharmaceutical industry also needs to take advantage of the recent
advances in biotechnology and information technology. The future of the industry will
be determined by how well it markets its products to several regions and distributes
risks, its forward and backward integration capabilities, its R&D, its consolidation
through mergers and acquisitions, co -marketing and licensing agreements.
#- #
º The pharma industry generally grows at about 1.5 -1.6 times the Gross
Domestic Product growth.
º In 2007-08, India exported drugs worth US$7.2 billion in to the US and Europe
followed by Central and Eastern Europe, Africa and Latin America .
º The Indian vaccine market which was worth US$665 million in 2007 -08 is
growing at a rate of more than 20%.
Every industry has its own sets of advantages and disadvantages under which they
have to work; the pharmaceutical industry is no exception to this. Some of the
challenges the industry faces are:
º Regulatory obstacles
º Lack of proper infra structure
º Lack of qualified professionals
º Expensive research equipments
º Lack of academic collaboration
º Underdeveloped molecular discovery program
º Divide between the industry and study curriculum
#-c ,#
º Capital Investment in Technology: Owing to the availability of advanced
technology at low costs, the companies can produce drugs at lower costs.
º Cost Effective: The filing cost of ANDAS and DMFs is comparatively low for
the Indian companies.
The company was founded in Amritsar in year 1937, when Ranjit Singh and Gurbux
Singh fused their names together to form Ranbaxy, accompany formed to distribute
medicine supplies by Japanese company Shionogi. It started as a distributor of
vitamins and anti-tuberculosis drugs. Bhai Mohan Singh joined the company as a
partner in 1952. rDIAZEPAM´ was the first product manufactured by Ranbaxy and
was most effective at that time to hit the Indian market and was vastly accepted.
Ranbaxy was established in June 16, 1961. In year 1973 Ranbaxy went public. After
the government¶s liberalization policy in year 1995, Ranbaxy was the 1 st Indian
company to become a MNC. Over the years, Ranbaxy has invested heavily and built
up considerable strength in manufacturing and marketing. Currently it has 14,000
strong team over 50 nationalities with sales over a 1 25 countries and manufacturing
in 7 countries.
Earlier in June 2008, Ranbaxy entered into an alliance with one of the largest
Japanese innovator companies, rDAIICHI SANKYO´. And the combined entity will be
catapulted to the no. 15 th position in the global pharmaceutical space. The company
is steadily moving towards its vision of becoming a 5 billion dollar company by the
year 2012. µDr. Tsutomu Une¶ and µMr. Arun SawhneyA| are the rChairman and
C.E.O´ of Ranbaxy respectively.
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Independent Director
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º Employees are not just the resources, they are the very purpose.
º Company hires the total men with body, mind and intellect, not just the hand.
º Aim is to utilize the full potential of all employees.
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º Achieving customer satisfaction is fundamental of business.
º Manage our operations with high concern for safety and environment.
+#
Ranbaxy was incorporated in 1961 and went public in 1973. For the year 2009, the
Company recorded Global Sales of Rs.73,441 Mn. ( US $ 1519 Mn). The Company
has a balanced mix of revenues from emerging and developed markets that
contribute 54% and 39% respectively. In 2009, North America, the Company's
largest market contributed sales of US $ 397 Mn, followed by Europe garnering US $
269 Mn and Asia clocking sales of around US $ 441 Mn. Earnings before tax were at
Rs.10,098 Mn. (US $ 209 Mn.) and earnings before tax were at Rs.3,107 Mn. (US $
64 Mn.), representing 4% margin to sales.
+
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º Consolidated sales were at USD 458 Mn (Rs 21,029 Mn), a growth of 22%
over Q2¶09. [Q2¶09: USD 368 Mn (Rs. 17,953 Mn)].
º Earnings before Interest, Tax, Depreciation & Amortization (EBIT DA) was at
USD 90 Mn (Rs. 4,168 Mn), a margin of 20% to sales. [Q2¶09: USD 11 Mn
(Rs. 568 Mn)].
º Profit after tax was USD 72 Mn (Rs. 3,320 Mn), a margin of 16%. [Q2¶09:
USD 139 Mn, (Rs. 6,931 Mn)]. Operational PAT, i.e. PAT excluding forex and
exceptional items was USD 100 Mn (Rs. 4,574 Mn). [Q2¶09: USD 2 Mn (Rs.
93 Mn)].
+
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º Consolidated sales were at USD 999 Mn (Rs 45,931 Mn), a growth of 42%
over H1¶09. [H1¶09: USD 682 Mn (Rs. 33,537 Mn)].
º Profit after tax was USD 282 Mn (Rs. 12,951 Mn), a margin of 28%. [H1¶09:
loss of USD (14) Mn, (Rs. (679) Mn)]. Operational PAT, i.e. PAT excluding
forex and exceptional items was USD 205 Mn (Rs. 9,442 Mn). [H1¶09: USD
(13) Mn (Rs. (639) Mn)].
º The Company¶s operating margins improved during the Quarter vis -à-vis
corresponding previous quarter, on account of sales of First -to-File (FTF)
products in the USA, and balanced growth across markets.
º Most markets/businesses grew during the Quarter with robust growth across
some of the Company¶s key markets/ businesses, including USA; Europe, led
by Romania; CIS led by Russia, and India.
º To sharpen its focus on generics, the Company reached an agreement to
transfer its New Drug Discovery Research assets, to Daiichi Sankyo India
Pharma Pvt. Ltd (DSIN).
º Ranbaxy launched Atorvastatin in Canada and South Africa. The launch in
Canada was under the Company¶s global settlement with Pfizer. In South
Africa, Ranbaxy was the first to launch a generic version in the market.
º alacyclovir, an FTF product in the USA, achieved a peak market share of
74% before the end of exclusivity during the Quarter.
º The Company introduced Daiichi Sankyo¶s innovative anti -platelet drug
Prasita (Prasugrel), in India. During the Quarter, Ranbaxy launched 31 new
products in India, including 3 in -licensed products.
º The Company made 32 filings and received 35 approvals for dosage forms
during the Quarter. For APIs, a total of 19 (15 APIs) filings were made, and 32
(15 APIs) approvals were received.
º The Company continues to co-operate with the US FDA and the Departmen t
of Justice, for early resolution of all outstanding issues. The Company¶s
facilities underwent inspections by other regulators, and Ranbaxy remains
compliant for supply.
º During the Quarter, emerging markets recorded sales of USD 230 Mn, a
growth of 6%, and contributed about 50% to global sales. Sales in developed
markets amounted to USD 203 Mn, a growth of 63%.
º North America region recorded sales of USD 160 Mn (Rs. 7,376 Mn) for the
Quarter, a growth of 100%. For H1¶10, revenues amounted to USD 424 Mn
(Rs. 19,482 Mn), a growth of 162% over the previous year, on the back of a
successful launch of alacyclovir.
º Europe recorded sales of USD 69 Mn (Rs. 3,195 Mn), a growth of 15% during
the Quarter. For H1, sales were at USD 137 Mn (Rs. 6,295 Mn), up 13% from
the previous year. In Romania, the growth momentum continued during the
Quarter, and the Company posted a strong increase of 27%, in revenue,
during Q2¶10.
º India sales were at Rs. 4,487 Mn (USD 98 Mn), almost at the same level as
previous corresponding quarter. Excluding tenders, sales grew by 11% during
the same period. For H1¶10, sales were at Rs. 8,375 Mn (USD 183 Mn).
Continuing its healthy performance, the Consumer Healthcare business
recorded a growth of 24% during H1¶10 and attained No. 1 rank in its
represented market during the Quarter.
º The CIS region recorded sales of USD 20 Mn (Rs. 927 Mn), a growth of 33%.
For H1¶10, sales were at USD 44 Mn (Rs. 2,024 Mn), up by 29% from
previous year.
º The Africa region achieved sales of USD 39 Mn (Rs. 1,774 Mn), a growth of
6% during the Quarter. For H1¶10, sales were at USD 77 Mn (Rs. 3,544 Mn),
up 16% from the previous year.
º The API business recorded sales of USD 26 Mn (Rs. 1,197 Mn), and USD 51
Mn (Rs. 2,362 Mn) for H1¶10.
º Rest of the World sales were at USD 45 Mn (Rs. 2,072), a de-growth of 11%.
For H1¶10, sales were at USD 83 Mn (Rs. 3,849 Mn), a de-growth of 10%.
This was largely on account of divestment of certain businesses in China and
Japan. Growth, excluding divested businesses, was 8% for the Quar ter.
c -
Ranbaxy is focused on increasing the momentum in the generics business in its key
markets through organic and inorganic growth routes. Growth is well spread across
geographies with focus on developed and emerging markets. It is the Company¶s
constant endeavor to provide a wide basket of generic and innovator products,
leveraging the unique Hybrid Business Model with Daiichi Sankyo. The Company will
also increasingly focus in high growth potential segments like accines and
Biogenerics. These new areas will add significant depth to the existing product
pipeline.
)
Ranbaxy views its R&D capabilities as a vital component of its business strategy that
will provide a sustainable, long -term competitive advantage. The Company has a
pool of over 1,200 R&D perso nnel engaged in path -breaking research.
Ranbaxy is among the few Indian pharmaceutical companies in India to have started
its research program in the late 70's, in support of its global ambitions. A first -of-its-
kind world class R&D centre was commissioned in 1994. Today, the Company has
multi-disciplinary R&D centers at Gurgaon, in India, with dedicated facilities for
generics research and innovative research. The R&D environment reflects its
commitment to be a leader in the generics space offering value added formulations
and development of NDA/ANDAs, based on its Novel Drug Delivery System (NDDS)
research capability.
The NDDS research at Ranbaxy focuses on maximizing the overall therapeutic and
commercial value of commonly prescribed pharmaceutical form ulations by
enhancing their performance and reducing their adverse event profile. Such
innovation also helps to improve the overall patient convenience and compliance .
The company's NDDS focus is mainly on the development of New Drug Applications
(NDA) / Abbreviated New Drug Applications (ANDAs) of oral controlled - release
products for the regulated markets. The Company's first significant international
success using the NDDS technology platform came in September 1999, when
Ranbaxy licensed its once-a-day Ciprofloxacin formulation on a worldwide basis to a
multinational Company.
Ranbaxy's in-house NDDS programs are primarily focused on the oral segment.
Inhalation (patented devices) and trans -dermal (patented adhesive polymers)
programs are also being pursu ed through collaborations.
In the oral NDDS space, Ranbaxy has already developed four platform technologies
namely Gastro Retentive, Modified Matrix, Multiparticulate and Aero Gel. Several
products leveraging these technologies have been successfully developed.
In July 2010, Ranbaxy¶s New Drug Discovery Research (NDDR) was transferred to
Daiichi Sankyo India Pharma Private Limited as part of the strategy to strengthen the
global Research and Development structure of the Daiichi Sankyo Group. While
NDDR will now become an integral part of Daiichi Sankyo Life Science Research
Center in India, based in Gurgaon, Ranbaxy will continue to independently develop
and later commercialize the anti -malarial new drug, Arterolane + PQP, which is
currently in Phase III trials, and will also explore the further development of late
stage programs developed by NDDR in the last few years, including the
development programs in the GSK collaboration.
Within Ranbaxy, R&D of Generics will now get a sharper focus, as the Compa ny is
increasingly working on more complex and specialist areas.
+
Corporate Social Commitment and Public Service is deeply embedded into the
cultural fabric of Ranbaxy. Over the years serious efforts have been directed towards
making a meaningful contribution to uplifting and transforming the lives of the
underprivileged . The Company is also extremely conscious of its duty and
responsibility towards the environment. We continue to make sincere efforts to
promote good health, social development and better environment, through various
Company programs that contribute to sustainable, all round growth.
In 1978, in the wake of the grim health scenario in India, Ranbaxy realized the
urgency to reach out to the underprivileged sections of society that had little or no
access to basic healthcare. The Company took a conscious decision to contribute
towards the national objective rHealth for All´. Towards this end, the rRanbaxy Rural
Development Trust´ was set up and the first well equipped mobile healthcare van
was introduced, in certain underserved areas of Punjab. As the programm e grew,
the Ranbaxy Community Healthcare Society (RCHS), an independent body, was
created, that is devoted to the health of the disadvantaged. Today, multiple well
equipped mobile healthcare vans and an urban family welfare centre, run by
Ranbaxy, benefit over 2 lakh people, in certain identified areas in the states of
Punjab, Haryana, Himachal Pradesh, Madhya Pradesh and Delhi. The programme is
based on an integrated approach of preventive, promotive and curative services,
covering areas of maternal child health, family planning, reproductive health,
adolescent health, health education including AIDS awareness.
During 2009, maternal and infant mortality were the focus of particular attention and
efforts in these areas were intensified in RCHS serviced area s. The results of these
interventions have been most encouraging and the general health profile of the local
community has shown further improvement in terms of coverage for immunization,
vitamin A deficiency and family planning. The problem of malnutritio n has been
addressed to a large extent and birth rates and infant mortality rates have declined
substantially. Amongst women, the risk of mortality due to pregnancy or child birth
has also been reduced when compared with the prevailing level of risk, in In dia and
other developing countries.
Ranbaxy has also dovetailed its CSR efforts in a manner that is synchronous with
the larger health goals of the State and Central Government. RCHS continued to
work actively on critical issues related to HI /AIDS, tuber culosis, malaria, polio, no
communicable chronic diseases and female foeticide. RCHS also continued its
partnership with the oluntary Health Association of Punjab for the project on
Reproductive Child Health (RCH), in the districts of Nawanshahar and Fate hgarh
Sahib, in Punjab and achieved the targets set under the RCH -II plan, of the
Government of India. Ranbaxy has entered into a Public Private Partnership (PPP)
with the Punjab State Government, to deliver healthcare services in identified
districts of Punjab.
c1
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1
Antenatal Care
Immunization ± (Tuberculosis, Diphtheria, Polio, Whooping Cough,
Tetanus & Measles)
Growth Monitoring
Safe Motherhood
Post natal care
Family Planning
Sterilization (Referral and follow up)
Provision of Family Planning Methods (Copper T, Oral Pills, Condoms)
''(
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1) U.S.A.
2) Ireland
3) Nigeria
4) China
5) Thailand
6) Malaysia
("F'c
º GURGAON [INDIA]
º LONDON [UK]
!(c
º DOULA (CAMEROON)
º KIE (UKRAINE)
º MOSCOW [RUSSIA]
º KAUNAS [LITHUANIA]
º NAIROBI [KENYA]
º YANGON [MYANMAR]
º ALMATY [KAZAKHSTAN]
º DUBAI [UAE]
º HARARE [ZIMBA E]
º CASABLANCA [MOROCCO]
º SOFIA [BULGARIA]
'c
Using the finest R&D and Manufacturing facilities, Ranbaxy Laboratories Limited
manufacture and markets generic pharmaceuticals, value added generic
pharmaceuticals, branded generics, active Pharmaceuticals (API) and intermediates.
The Company remains focused on ascending the value chain in the marketing of
pharmaceutical substances and is determined to bring in increased revenues from
dosage forms sales.
Ranbaxy's diverse product basket of over 5,000 SKUs available in over 125
countries worldwide encompasses a wide therape utic mix covering a majority of the
chronic and acute segments. Healthcare trends project that the chronic treatment
segments will outpace the acute treatment segments, primarily driven by a growing
aging population and dominance of lifestyle diseases. Our robust performance in
Cardiovasculars, Central Nervous System, Respiratory, Dermatology, Orthopaedics,
Nutritionals and Urology segments, clearly indicates that the Company has
strengthened its presence in the fast-growing chronic and lifestyle disease
segments.
8;
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º al acyclovir
º Simvastatin
º Co-Amoxyclav
º Ciprofloxacin and Combinations
º Amoxicillin and Combinations
º Isotretinion
º Ketorolac Tromethamine
º Loratadine and Combinations
º Ginseng + itamins
º Atorvastatin and Combinations
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º Project r IRAAT´ was launched to achieve top slot in the market.
º Sales for the year 2009 in domestic market were US $ 1.52 Bn (Rs 7,344
crores); PBT was US $ (Mn (over RS 1000 crores); PAT was US $64 Mn (Rs
311crores).
º Ranbaxy delivers global sa les for the year 2009 was US $ 1519 Mn (Rs
73,441 Mn) which reflects a modest growth over 2008 sales of RS. 72,555
Mn. There was a turnaround in the profitability of the company with Earnings
before Interest Tax Depreciation and Amortisation (EBITDA) for t he year 2009
at Rs. 11,991 Mn against a loss of Rs. 2,626 Mn for the year 2008. Where
emerging markets contributed 54% of sales, while developed markets
accounted for 39% and API was 7%.
3c,
Ranbaxy is one of the leading pharmaceutical Companies in India
commanding a market share of around 5%. The Company has clocked sales
of USD 293 Mn in 2009 in India. Growing ahead of the market, the Company
has enhanced its competitive position in the dome stic market through its
focused approach. The Company¶s business has been realigned to its
customer groups and investments have been made in high growth segments.
These efforts have resulted in strengthening its Chronic franchise (Life Style
led) as well as has reinforced its leading position in the Acute segment.
c+# #
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CHERICOF Complete Cough CCA - Cough, Cold &
1
COUGH SYRUP Syrup for family Allergy
CHERICOF Cough remedy CCA - Cough, Cold &
2
SOFTGEL capsules Allergy
Appetite enhancer-
3 EATEASE GI - Gastro-intestinals
Children (Herbal)
Garlic oil for all round
4 GARLIC PEARLS GI - Gastro-intestinal
health
5 GESDYP Digestive Enzymes GI - Gastro-intestinal
CCA - Cough, Cold &
6 OLESAN GEL Cold rub (Herbal)
Allergy
OLESAN Cough & sore throat CCA - Cough, Cold &
7
LOZENGES cure ( Herbal) Allergy
Nasal decongestant oil CCA - Cough, Cold &
8 OLESAN OIL
(Herbal) Allergy
Effervescent digestive
9 PEPFIZ GI - Gastro-intestinal
enzymes
RE ITAL Ginseng, vitamins & MS- itamins, Minerals
10
SOFTGELS minerals & Supplements
Ginseng, vitamins & MS- itamins, Minerals
11 RE ITAL LIQUID
minerals & Supplements
Soy Protein MS ± itamins,
12 RE ITALITE
Supplement Minerals & Supplements
Complete Pain relief
13 OLINI GEL ANALGESIC-Topical
Gel
Complete Pain relief
14 OLINI SPRAY ANALGESIC-Topical
Spray
Complete Pain relief
15 OLINI TABS ANALGESIC-Oral
tabs
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º ery low level of Biotechnology in India and also for New Drug Discovery
Systems.
º Low level of strategic planning for future and also for technology forecasting.
-
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º Block µA¶ is used exclusively for manufacturing tablet products with an instal led
capacity of 240 million capsules per annum.
º Access to warehouse from both the blocks is through the separating corridors
and air locks.
º The access to warehouse from both the blocks is through the separating
corridors and air locks.
º The ranges of products which are manufactured in this plant are Quinolines,
Anti-Bacterial and Anti-Histamines.
º 90% of products which are manufactured in this pl ant are exported to various
countries like USA, U.K., Spain and Canada.
$
#
This plant is licensed by the Department of Health and Family Welfare, Government
of Himachal Pradesh, the official licensing authority to manufacture and pack various
formulations (tablet and capsule dosage forms).
#
The tablet products manufactured include a range of products like Quenelle
Antibacterial, Anti-Histaminic and Anti-Ulcerative. The brand names and the generic
names of the products are as under:-
+
º CIFRAN (CIPROFLOXACIN)
º HISTAC (RANITIDINE)
º NORBACTINE (NORFLOXACIN)
º TREXYL (TEREFENADIE)
º CLAMPOSE (DIAZEPAM)
º REXPAR
º PYLOBACT
º OPLOXACIN (OFLOXACIN)
º CIPRO ± OD (HISINOPREL MONOHYDRATE)
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3
º RE ITAL CAPSULES
º CHERRICOF SOFTGEL CAPSULES
º TARAXOCIN CAPSULES
º ISOTRETINOIN CAPSULES
º GARLIC PEARLS CAPSULES
º GINSENA CAPSULES
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º The plant is further divided into Administrative Block, Quality Control Lab.,
Tablet and Capsule Block, Maintenance Department, Warehouse, Packaging
Lab. And Effluents Treatment Plant (ETP).
º Access to warehouse from both the blocks is through the separating corrid ors
and air locks.
º All the products manufactured in this plant are exported to the foreign markets
like USA, FRANCE, JAPAN and CANADA.
#
The tablets and Capsules products manufactured there include a range of products
which are very costly in terms of money. As the API (Active Pharmaceutical
Ingredients) costs from Rs 80 lakhs to Rs 1.5 crores per kg. All the products are
manufactured for the foreign markets. The products manufactured are for the
treatment of µCancer¶ and for µLungs & Liver Transplant¶ the brand names and the
markets of the products are as under: -
An organization¶s goals can be achieved only when people put in their efforts. How
to ascertain whether an employee has shown his or her best performance on a given
job?
It is the systematic evaluation of the individual with respect to his or her performance
on his or her potential for the development.
º Performing rating
º Employees assessment
º Employees performance review
º Personnel appraisal
º Performance evaluation
º Employees evaluation
º Merits rating
3
1. The concept of Performance Appraisal dates back to the First World War and was then
called rMerit Rating Programme´. Over a period of time, this concept has been through an
ocean of change. The areas of evaluation have also changed.
2. According to Carl Heyel, author/editor on management, philosopher and teacher,
rperformance appraisal is the process of evaluating the performance and qualifications of
the employees in terms of job requirements, for administr ative purposes such as
placement, selection and promotion, to provide financial rewards and other actions which
require differential treatment among the members of a group as distinguished from actions
affecting all members equally´.
,
1. A few decades ago, the employee used to be appraised by his department head. The
department head used to communicate his feedback and comments only to the immediate
superior of the employee. Thus the feedback was kept confidential in nature. As time
passed by, the immediate superior started appraising his subordinate¶s performance and
sending his confidential report to the department head. These were the periods when the
employee was not included in his appraisal process. The decisions used to be taken by his
superiors relating to his pay hike, promotion etc. Thus the system was non -transparent.
2. The current process of performance appraisal is much more open and gives some scope
for self-appraisal by the employee. The self -appraisal is followed by a joint discussion wit h
superior and then a decision is taken by the department head on his promotion, pay hike
etc. The feedback relating to his performance is directly given to the employee. Thus
performance appraisal process has gone through the phase of non -transparency to
transparency
+
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º Salary
º Promotion
º Retention/termination
º Recognition of performance
º Layoffs
º Identification of poor performers
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4. To decide upon a pay raise where (as in the unorganized sector) regular pay
scales have not been fixed.
5. To let the employees know where they stand insofar as their performance is
concerned and to assist them with constructive criticism and guidance for the
purpose of their development.
Broadly, performance appraisal serves four objectives ±
i. Developmental uses.
ii. Administrative decisions.
iii. Organizational objectives.
iv. Documentation purposes.
º Feedback mechanism,
º Consistency between organizational strategy and job behaviour, and
º Consistency between organizational values and job behaviour.
|
|
|
|
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$
#+
A five-step approach to conducting Performance Appraisal is recommended:
|
1+#+# # 4
#+12 4
#
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|
|
|
|
|
|
+,
º ##-#+, 4This traditional form of appraisal, also known as
"Free Form method" involves a description of the performance of an
employee by his superior. The description is an evaluation of the performance
of any individual based on the facts and often includes examples and
evidences to support the information. A major drawback of the method is the
inseparability of the bias of the evaluator.
º c ,3 , 4 This is one of the oldest and simplest techniques
of performance appraisal. In this method, the appraiser ranks the employees
from the best to the poorest on the basis of their overall performance. It is
quite useful for a comparative evaluation.
º
#4 A better technique of comparison than the straight
ranking method, this method compares each employee with all others in the
group, one at a time. After all the comparisons on the basis of the overall
comparisons, the employees are given the final ranki ngs.
º
+
# , #4 In this method of Performance appraisal, the
evaluator rates the employee on the basis of critical events and how the
employee behaved during those incidents. It includes both negative and
positive points. The drawback of this method is that the supervisor has to note
down the critical incidents and the employee behaviour as and when they
occur.
|
,
|
º GË; #+ , : 360 degree feedback, also known as 'multi -
rater feedback', is the most comprehensive appra isal where the feedback
about the employees¶ performance comes from all the sources that come in
contact with the employee on his job.
360 degree respondents for an employee can be his/her peers, managers (i.e.
superior), subordinates, team members, customers, suppliers/ vendors -
anyone who comes into contact with the employee and can provide valuable
insights and information or feedback regarding the "on -the-job" performance
of the employee.
GË; #+,#$ +
# :
1. Self appraisal
2. Superior¶s appraisal
3. Subordinate¶s appraisal
4. Peer appraisal.
# 1 #$$
#+4
º c 4 Traditional performance appraisals involve a supervisor
and supervisee, both of which have limited perspectives. As with any
situation, limited perspectives lead to a limited amount of information by which
to judge performance.
If a manager is busy supervising several people, as well as tasks and other
projects, then there will be limited time to take in the full scope and practice of
the performance of the supervisee. As an alternative, many industries today
are utilizing 360-degree feedback, which takes into account the relatio nships
that an employee has with peers, customers, clients, supervisors and those
whom the supervisee is responsible for overseeing.
Furthermore, the employee naturally will want to bargain for more money
focusing on their strengths and the management will want to emphasize the
constructive areas of performance evaluation in order to keep from giving
raises, since money is a limited resource in any organization. This adds to the
stress of the review.
( +#$$$
1#+12
º Minimise interruption
º Welcome, at ease
º Listen
º Be specific
º Complete form
$
#+0-#
Performance Appraisal for managers is known as performance management system.
Managers have to set certain .!- # + # %!E#&/, which serves as the
base of performance measurement.
KRA¶s mentions the critical tasks/performance areas that the appraisee needs to
focus on in the coming year. The appraiser and appraisee need to participate in
setting the KRA¶s. There can be maximum of 5 and minimum of 3 KRA¶s. The
importance of each KRA is designated in terms of percentage (%) and is writ ten in
the percentage weightage column. The total in the percentage weightage column of
all KRA¶s should be equal to 100. The KRA¶s are set at the beginning of the year.
Then they are evaluated in the midterm (in June) .
The KRA form is used to share the appraiser¶s expectations with the appraisee.
Appraiser have to clarify major areas of planned effort that are to be initiated during
the performance period and also how the appraiser expect the planned results to be
achieved.
They also work on training plans. Where the appraiser and appraisee will mutually
decide on immediate training needs. Like new updations in SAP.
º Score5 ± Exceptional
º Score 4 ± Exceeds Expectations
º Score3 ± Meets Expectations
º Score2 ± Needs Improvement
º Score1 ± Below Expectation