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Table of Content s
1. Financial Updates.....................................................1
2.Solutions Updates......................................................7
5.Miscellaneous Updates...........................................34
Executive Commentary
“The pharmaceutical industry experienced a transformation and FosunPharma
will be firmly committed to the path of innovation and internationalization. We
believe that our efforts in innovation will help FosunPharma realize its
innovation transformation. The steady international-oriented development will
make us more competitive internationally in terms of operation standards and
market expansion.” President and CEO of FosunPharma said.
$1.26
Executive Commentary
Description 3
Amgen announced that it has entered into an agreement with
Celgene Corporation in connection with its previously
announced merger with Bristol-Myers Squibb Company to
acquire worldwide rights to Otezla® (apremilast), the only oral,
non-biologic treatment for psoriasis and psoriatic arthritis, and
certain related assets and liabilities, for $13.4 billion in cash, or
approximately $11.2 billion, net of the present value of $2.2
billion in anticipated future cash tax benefits.
Executive Commentary
"The acquisition of Otezla offers a unique opportunity for Amgen to provide
patients an innovative oral therapy for psoriasis and psoriatic arthritis that fits
squarely within our portfolio and complements our Enbrel® and AMGEVITA®
brands," said Chairman and chief executive officer at Amgen. "We will take
advantage of our 20 years of experience in inflammatory disease to realize the
full global potential of Otezla as an affordable option for patients with these
serious, chronic inflammatory conditions."
Executive Commentary
"This acquisition brings expertise in advanced imaging and robotics as well as a
robust product pipeline that add to Stryker’s portfolio and will allow the Spine
division to provide more complete procedural solutions, including sales, service,
and support," said Stryker’s Group President, Orthopaedics and Spine. "We look
forward to working together to advance Stryker’s mission to make healthcare
better and accelerate our pursuit of category leadership in Neurotechnology,
Orthopaedics, and Spine."
Description
5
Boston Scientific Corporation announced the completion of its acquisition of BTG
plc. pursuant to the previously announced scheme of arrangement. BTG develops and
commercializes products used in minimally-invasive procedures targeting cancer and
vascular diseases, as well as specialty pharmaceuticals. BTG has three key
businesses, the largest of which is its highly-differentiated Interventional Medicine
portfolio that encompasses interventional oncology therapeutic technologies for
patients with liver and kidney cancers, as well as a vascular portfolio for treatment of
deep vein thrombosis, pulmonary embolism, deep venous obstruction and superficial
venous disease.
Executive Commentary
"The addition of the BTG Interventional Medicine portfolio reinforces our
category leadership strategy and enables us to offer best-in-class technologies,
unparalleled clinical evidence and a strengthened commercial infrastructure to
support physicians treating some of the most challenging diseases impacting
patient health around the world," said Chairman and chief executive officer,
Boston Scientific. "Leveraging the employee talent and clinical and commercial
expertise of these two high-performing organizations will generate continued
innovation and access so that we may advance patient care in ways that neither
company could do alone."
For more details, please click the link below:
https://news.bostonscientific.com/2019-08-19-Boston-Scientific-Closes-Acquisition-of-BTG-plc
Description
6
H. Lundbeck A/S (Lundbeck) and Alder BioPharmaceuticals announced a definitive
agreement for Lundbeck to acquire Alder. Under the terms of the agreement,
Lundbeck will commence a tender offer for all outstanding shares of Alder, whereby
Alder stockholders will be offered an upfront payment for USD 18.00 per share in
cash, along with one non-tradeable Contingent Value Right (CVR) that entitles them
to an additional USD 2.00 per share upon approval of eptinezumab by the European
Medicines Agency (EMA), representing a total potential consideration of USD 20.00
per share. The transaction is valued at up to USD 1.95 billion (approximately DKK
13 billion) net of cash, on a fully diluted basis.
Executive Commentary
President and CEO of Lundbeck, commented “Alder is an excellent strategic fit for
Lundbeck’s focused expertise in brain diseases and organizational capabilities. This
transaction flows from our strategic intent to Expand and Invest to Grow. Migraine
prevention is an attractive indication for us that leverages our specialized commercial
expertise in delivering medicines for brain diseases. We expect the global launch of
eptinezumab for the preventive treatment of migraine, as well as the further potential
development of the product in additional indications, to accelerate Lundbeck’s growth
in the coming years.”
Solution Updates
Healthcare Industry
Solution Descriptio n
7
Solution Descriptio n
8
Roche Diagnostics announced that the US Food and Drug
Administration (FDA) has cleared its cobas pro® integrated
solutions, a new generation of Serum Work Area (clinical
chemistry and immunochemistry) laboratory solution, designed
to optimize lab operations. With the cobas pro integrated
solutions, laboratories are now able to run tests faster on less
equipment, automate manual tasks and deliver results more
quickly to aid in treatment decisions. Diagnostic laboratories
are a critical component of the global healthcare system with in
vitro diagnostics influencing up to 70% of all clinical decisions
while accounting for only about 2% of total healthcare
spending.1,2 Together, medical and lab professionals play a key
role in delivering optimal patient care, yet they face increasing
pressure to manage a growing number of samples, while
delivering quality results faster and rising profitability.
Solution Descriptio n
9
Medtronic plc, the global leader in medical technology, services and solutions,
commercial release in Europe and the Middle East this fall, subject to local
professionals and their patients with either type 1 and type 2 diabetes to see
accurate glucose levels and trends over time to develop more optimal diabetes
therapy plans.The Envision Pro system was designed with ease of use as a top
priority. For instance, patients no longer need to calibrate the CGM through
physician, as both pieces are now fully disposable. The recorder communicates
that the healthcare provider obtains the data seamlessly and can run reports
Solution Descriptio n
10
Roche announced that the European Commission has approved Tecentriq® (atezolizumab)
plus chemotherapy (Abraxane® [paclitaxel protein-bound particles for injectable
suspension (albumin-bound); nab-paclitaxel]) for the treatment of adult patients with
unresectable locally advanced or metastatic triple-negative breast cancer (TNBC) whose
tumours have PD-L1 expression (≥1%) and who have not received prior chemotherapy for
metastatic disease. Roche’s VENTANA PD-L1 (SP142) Assay is now CE marked and
commercially available in the European Union as an aid for identifying patients with
TNBC eligible for treatment with the Tecentriq combination.This approval is based on the
results from the Phase III IMpassion130 study. Progression-free survival (PFS) results
demonstrated a statistically significant benefit for Tecentriq in combination with
nab-paclitaxel and showed that Tecentriq plus nab-paclitaxel significantly reduced the risk
of disease worsening or death (PFS) by 38% compared with nab-paclitaxel alone (median
PFS=7.5 vs 5 months; hazard ratio [HR]=0.62, 95% CI: 0.49-0.78, p<0.0001) in people
who were tested positive for PD-L1 expression on tumour-infiltrating immune cells. At the
second interim analysis, Tecentriq and nab-paclitaxel showed a clinically meaningful
overall survival (OS) improvement of seven months vs placebo and nab-paclitaxel in the
PD-L1-positive population (median OS=25.0 vs 18.0 months; HR=0.71, 95% CI: 0.54
–0.93). OS results in the PD-L1-positive population were not formally tested due to the
hierarchical design of the study as statistical significance was not met for OS in the
intention-to-treat (ITT) population (median OS=21.0 vs 18.7 months; HR=0.86, 95% CI:
0.72–1.02, p=0.078).
Solution Descriptio n
11
Roche announced that the European Commission has approved and granted
marketing authorisation for Tecentriq® (atezolizumab) in combination with
chemotherapy (carboplatin and Abraxane® [albumin-bound paclitaxel;
nab-paclitaxel]), for the initial (first-line) treatment of adults with metastatic
non-squamous non-small cell lung cancer (NSCLC) who do not have EGFR mutant
or ALK-positive NSCLC.This approval is based on results from the Phase III
IMpower130 study, which demonstrated that the Tecentriq combination therapy
helped people live significantly longer, compared with chemotherapy alone (median
overall survival [OS]=18.6 versus 13.9 months; hazard ratio [HR]=0.79; 95% CI:
0.64–0.98; p=0.033) in the intention-to-treat wild-type (ITT-WT) population.1 The
Tecentriq-based combination also significantly reduced the risk of disease worsening
or death (progression-free survival [PFS]) compared with chemotherapy alone
(median PFS=7.0 versus 5.5 months; HR=0.64; 95% CI: 0.54–0.77; p<0.0001) in the
ITT-WT population.1 The safety profile of the Tecentriq combination therapy was
consistent with that observed in previous studies.Lung cancer is the leading cause of
cancer death globally, and each year 1.76 million people die as a result of the disease,
which translates into more than 4,800 deaths worldwide every day.2 NSCLC is the
most prevalent type of lung cancer, accounting for around 85% of all cases.3
Solution Descriptio n
12
R&R Description
14
Roche has again been recognised as one of the most sustainable
companies in the Pharmaceuticals index of the Dow Jones
Sustainability Indices (DJSI). This is based on an in-depth analysis of
economic, social and environmental performance. The DJSI family of
indices serves as a benchmark for investors who integrate
sustainability considerations into their portfolios. Roche has
maintained its leadership through its excellent sustainability strategy,
which is fully embedded in the company’s business and culture.For
Roche, it is a priority to ensure that medicines and diagnostics reach
the people who need them. This is why, the company is committed to
constantly identifying and eliminating barriers to access to healthcare.
For example, Roche undertook an evaluation of the supply chain in
Kenya, Ethiopia, Sudan, Côte d'Ivoire, Nigeria, Ghana to develop new
lean supply chain models. This included removing complexity,
improving quality and moving towards directly supplying governments
and points of care in the countries. Reorganising the supply chain
reduced lead time from Switzerland to local warehouses significantly,
in the case of Kenya from 90 to 21 days.
R&R Description
16
Good Neighbor Pharmacy – a national independent pharmacy network
offered through AmerisourceBergen – announced that it has been
ranked “Highest in Customer Satisfaction with Chain Drug Store
Pharmacies” in the J.D. Power 2019 U.S.Pharmacy Study. This marks
the eighth time that Good Neighbor Pharmacy has earned the
achievement in the last 10 years.This year, Good Neighbor Pharmacy
ranked the highest in overall satisfaction among chain drug store
pharmacies. Good Neighbor Pharmacy received a score of 914 while
the average was 842. Additionally, Good Neighbor Pharmacy ranked
highest in five factors: Prescription Ordering and Filling Process;
Pharmacist; Non-Pharmacist Staff; Cost Competitiveness; and
Store.The customer service recognition follows AmerisourceBergen’s
recent unveiling of new tools that help pharmacies connect with
customers in new and meaningful ways. These tools include
medication adherence support, a market analysis report and expanded
digital marketing services. The resources offer pharmacists solutions
that fit within their existing workflows and empower them to establish
strong relationships with their customers.
R&R Description
18
Baxter International Inc., a leading global medical products company,
announced it has again been named to the Dow Jones Sustainability Indices
received annually since the indices were launched in 1999 and 2005,
Baxter scored in the top five percent of companies assessed within the health
R&R Description
19
The 2019 Shanghai Top 100 Enterprises Conference, jointly organized
the award.
2018" and other high-profile enterprises. A list of industry trends. Deputy secretary of
Shanghai Pharmaceuticals received the top 100 awards on behalf of the company.
In this selection, Shanghai Pharmaceutical Group continued to rank sixth in the “Top
100 Enterprises in China's Pharmaceutical Industry in 2018” and won the “Top 25
in 2019”; the joint venture Shanghai Hehuang Pharmaceutical Co., Ltd. was awarded
R&R Description
22
Regeneron Pharmaceuticals, Inc. announced that the company
was added to the Dow Jones Sustainability World Index (DJSI
World) for the first time. Regeneron is one of only four
companies in the biotechnology sector to be included on the
DJSI World list. DJSI World is a leading global index
comprised of corporate leaders in environmental, social and
governance (ESG) practices, which recognizes the top 10
percent most sustainable companies in each industry.DJSI
World is considered the gold standard for measuring corporate
ESG practices. It is published by S&P Dow Jones Indices, one
of the world's leading index providers, together with
RobecoSAM, which specializes in ESG data and
benchmarking. This year, more than 4,500 global companies
were invited to participate in the evaluation process.
Description 23
CVS Pharmacy, the retail division of CVS Health announced a collaboration
with Google Photos on their new same-day, print-to-store experience.
Consumers can now order high-quality 4x6 prints directly from Google Photos
for same-day pick up at more than 7,400 CVS Pharmacy locations nationwide.
The printing service for CVS Pharmacy, powered by Kodak Moments' vast
global retail network and enhanced software technology, begins rolling out
across the country and will be broadly available by this October. Consumers are
increasingly looking for convenient and easy ways to print out their digital
photos, according to a 2018 Kodak Moments U.S. Attitudes and Usage Study
conducted by Keypoint Intelligence InfoTrends, 64% of US consumers print
photos and over a third plan to print more in the future. Originally launched in
2015, Google Photos serves as the home for photos and videos, helping people
save, organize and share their photos and videos. Accessible via iOS or Android
as well as through Google Photos on the web, the same-day printing service is
made possible through participation in the Kodak Moments Prints partner API
program, so consumers can effortlessly bring their digital snapshots to life at
participating CVS stores throughout the U.S.
Sanofi and Abbott partner to integrate glucose sensing and insulin delivery
technologies to help change the way diabetes is managed
Description 24
Sanofi and Abbott are partnering to integrate glucose sensing and insulin
delivery technologies that would help to further simplify how people with
diabetes manage their condition. The two companies will take an
innovative approach to connected care by developing tools that combine
the revolutionary FreeStyle Libre technology with insulin dosing
information for future smart pens, insulin titration apps and cloud
software.The non-exclusive collaboration will initially enable data sharing,
at the consent of the user, between Abbott’s FreeStyle Libre mobile app
and cloud software and Sanofi’s connected insulin pens, apps and cloud
software that are currently in development. This data sharing will enable
both people with diabetes and their doctors to make better informed
treatment decisions around medication, nutrition and lifestyle.Sanofi is
currently working to provide connected pens, apps and cloud software that
will be compatible with the FreeStyle Libre system and its compatible
digital health tools. The two companies aim to bring this to people with
diabetes within the next few years, pending local regulatory approvals.
Description 25
Medtronic plc, and Novo Nordisk A/S announced a collaboration that will develop
solutions to integrate insulin dosing data from future Novo Nordisk smart insulin
pens into Continuous Glucose Monitoring (CGM) devices from Medtronic, such as
the Guardian™ Connect system. People with diabetes spend an average of one hour a
day on self-care, amounting to a full two years devoted exclusively to their disease
people with diabetes and their healthcare professionals and caregivers (with
permission from the person with diabetes) will be able to automatically track these
two important items in a single place, giving people living with diabetes one less
thing to think about in the daily management of their condition. Further, being able to
view both glucose and insulin data together can facilitate more productive
conversations between people and their doctors, enabling more informed decisions
on how to better manage glucose levels and increase Time in Range (TIR) - the
percentage of time people with diabetes spend in the optimal glycaemic range of
70-180 mg/dL.3
Description 26
Aetna, a CVS Health company, has signed an agreement to add
Description 27
Blue Cross and Blue Shield of Minnesota and Minnesota Oncology, a practice in The
US Oncology Network, announced a five-year agreement that will change the way
cancer care is paid for and managed in order to deliver optimal health outcomes at
lower costs.This collaboration, which takes effect September 1, 2019, will make Blue
Cross and Minnesota Oncology jointly accountable for the overall cost of cancer care
provided to Blue Cross members through a value-based risk arrangement. The terms
of the arrangement are based on the principle that effective outcomes for patients are
determined by the quality of care provided – not the quantity.With an enhanced focus
on patient-centric healthcare, clinical staff at Minnesota Oncology will offer care
coordination services on an individualized basis for Blue Cross members. This
approach will help to ensure that the comprehensive care model already in place
consistently delivers the best possible outcomes by providing appropriate, medically
necessary care at the right time and place.The five-year collaboration will include an
agreed-upon set of quality metrics based on the latest scientific research and proven
clinical guidelines. Minnesota Oncology will be responsible for ensuring continued
alignment with evidence-based best practices and, as a result, will no longer be
required to secure prior authorization from Blue Cross for coverage of selected
services that are typically associated with high rates of overutilization.
Description 28
McKesson, a leading provider of third-party logistic (3PL) services, patient access support
and specialty pharmacy solutions, and TrakCel, the software developer for cell and gene
therapy supply chain tracking and orchestration systems, announce a collaboration to
support cell and gene therapy late-stage developers. The collaboration will integrate both
companies’ supply chain tracking and patient access services to enable a more efficient path
for the industry to develop the next-generation of commercial therapies. Combining
TrakCel’s data tracking and personalized medicine orchestration software system with
McKesson’s existing high-touch patient platform, as well as both companies’ expertise and
support, will provide an end-to-end solution for the cell and gene therapy industry to
manage the entire therapeutic supply chain. McKesson and TrakCel will begin by
developing an initial solution design. The combined solutions will then be offered to
individual clients that would specifically benefit from this combination. The blend of these
product suites is specifically designed for the increasing number of developers approaching
the commercial launch of cell and gene therapies. The integrated platform enables the
scale-up of products towards market delivery. This includes automatic scheduling of
product-specific workflows across multiple supply chain partners and care team members,
and validated chain-of-identity tracking to guarantee correct drug product delivery. These
capabilities ensure that the patient receives the correct, uncompromised treatment at the
right time.
Description 29
Description 30
Guangzhou Pharmaceutical Group Co., Ltd. and Kangmei Pharmaceutical Co.,
Ltd. held a signing ceremony for the strategic cooperation agreement at the
headquarters of Guangzhou Pharmaceutical. The two parties will integrate the
advantageous resources in the field of Chinese medicine and give full play to
their respective advantages in the management of Chinese herbal medicine
supply chain. Cooperation in product channel services and other areas to jointly
help "revitalize Da Nan medicine." During the period, the two sides conducted
in-depth exchanges on the prospects for future cooperation. Li Chuyuan said
that Kangmei Pharmaceutical adheres to the remarkable achievements in the
inheritance and innovation of Chinese medicine culture, successfully builds a
comprehensive industrial chain resource integration platform, and has a flexible
operation system to realize the national distribution of “smart +” big health
industry, leading the industry, and is a private enterprise in the Chinese
medicine industry. Representatives, models. As a state-owned enterprise, GPHL
maintains its own unique characteristics in the development of the big health
industry. This is in line with the development of Kangmei Pharmaceutical's
main business. There are still many space for further cooperation in the field of
big health industry.
Eisai Enters Into Business Alliance with CogstateFor Exclusive Development And Commercialization
Description 31
Eisai Co., Ltd. announced that it has entered into a business alliance
agreement for exclusive development and commercialization of a
cognitive function test - Cogstate Brief Battery (CBB) - developed by
Cogstate Ltd., in Japan as a digital tool for self-assessment of cognitive
function. The CBB consists of four tests, each measuring different
cognitive domains: psychomotor function, attention, working memory,
and learning, and it has been developed and already in use as a digital
tool for self-assessment of cognitive function overseas, including the
United States. Eisai will aim to raise awareness of cognitive function
by developing and making widely available the CBB in Japan jointly
with Cogstate as a simpler digital tool for self-assessment of cognitive
function, which can be used at various locations such as at home and
community events. With this tool, it is expected to have opportunities
to review lifestyle and to consult with specialists and primary care
physicians by objectively checking the changes in cognitive function.
It is important to note that this tool is not an alternative for medical
examination and diagnosis by qualified medical professionals.
Description 32
Royal HaskoningDHV, CEAD and DSM announced that
they have designed the first lightweight 3D printed FRP
pedestrian bridge prototype using a composite material. It
consists of a glass filled thermoplastic PET (Arnite®) and
is combined with continuous glass fibers which are added
in the 3D printing process. This unique combination
offers high strength with extreme versatility and
sustainability.Together, the three companies are leading a
revolution in bridge construction and design. To build a
3D printed bridge Royal HaskoningDHV, an international
engineering and project management consultancy,
partnered with DSM, a global science-based company in
nutrition, health and sustainable living and pioneer in 3D
printing materials, and CEAD, supplier of 3D printing
equipment on the frontier of large-scale composite
additive manufacturing.
For more details, please click the link below:
https://www.dsm.com/corporate/news/news-archive/2019/2019-09-03-royal-haskoningdhv-cead-and-dsm-design-first-lightweight-3d-printed-bridge-using-frp.html
Description 33
Allergan plc a leading global pharmaceutical company with a
heritage of more than 70 years in eye care, and Molecular
Partners a clinical-stage biotechnology company developing a
new class of drugs known as DARPin® platform, announced
that the U.S. Food and Drug Administration (FDA) has
accepted a Biologics License Application (BLA) and the
European Medicines Agency (EMA) has validated a Marketing
Authorisation Application (MAA) for Abicipar pegol, a novel,
investigational DARPin® therapy, in patients with neovascular
(wet) age-related macular degeneration (nAMD). The FDA is
expected to take action on the BLA mid-2020. A decision from
the European Commission is expected in the second half of
2020.The BLA and MAA filings are based on data from two
Phase 3 trials, CEDAR and SEQUOIA, which supported the
non-inferior efficacy of the Abicipar quarterly dosing regimen
to maintain vision gains with more than 50 percent fewer
injections versus ranibizumab (13 vs. 6) dosed monthly in the
first year.
Miscellaneous Updates
Healthcare Industry
Description
34
LabCorp® , a leading global life sciences company that is
deeply integrated in guiding patient care, announced that
its Covance Drug Development business celebrated the
opening of its new R&D Center in Shanghai, China,
which is now its largest facility in the Asia Pacific region.
The opening ceremony was attended by Chao Yang, vice
chairman of the Shanghai Municipal Commission of
Commerce; Feng Huang, chairman of the Shanghai
Association of Foreign Investment; John Ratliff, CEO,
Covance; and Honggang Bi, Ph.D., corporate vice
president of Covance and general manager, China, as well
as biopharmaceutical and biotech industry leaders,
clinical research key opinion leaders, research partners
and local dignitaries.
Description 35
Illumina, Inc. has been notified of an unsolicited
“mini-tender offer” by TRC Capital Corporation (“TRC”)
to purchase up to 500,000 shares of Illumina common
stock at a price of $268.80 per share in cash. TRC’s offer
is subject to a number of conditions, including TRC’s
ability to obtain sufficient financing. By its terms, TRC’s
offer will expire at 12:01 a.m., New York City time, on
Thursday, October 3, 2019, but TRC may extend the offer,
or terminate it, before the expiration date. Illumina is not
affiliated or associated in any way with TRC, its offer or
the offer documentation. Illumina recommends that
stockholders not tender their shares in response to TRC's
unsolicited offer because, among other things, it deprives
stockholders who tender their Illumina shares of the
potential opportunity to realize greater long-term value in
their investment.
For more details, please click the link below:
https://www.illumina.com/company/news-center/press-releases/press-release-details.html?newsid=3a22851b-22fa-42db-9a23-8e8a4624abb3
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