TRAINING ON PROCESS
Chemical Engineer’s Special ENGINEERING ACTIVITIES IN API
MANUFACUTIRNG
PHARMACEUTICAL INDUSTRIES
SCOPE
The Scope of this program is to train the participants on the basics of technology involved in
manufacturing of bulk drugs in Pharmaceutical industry. Training program provides a basic
understanding on the manufacturing processes and a quick deep dive into the activities which are
a part of chemical engineers job responsibility in Pharmaceutical industries. The program
provides detailed and consolidated demonstration on the roles and responsibility of a chemical
engineer during process development at lab.
WHO ARE WE
We are a group of engineers with expertise in Process engineering activities and having a great
exposure in Bulk drug manufacturing. We assure the participants that who attends all the
planned sessions will gain a mix of technical and practical knowledge which can be gained in the
beginning 3 + years of industrial exposure.
WHY TO ATTEND
In the recent times of recruitment, the manufacturing companies would prefer to recruit
experienced individuals rather than hiring fresher’s, as it would take time to train the individuals
and the period would be like an investment for the company. Here we provide you all the basics
of activities which a chemical engineer would come across in his daily routine as a part of job
responsibility. Hence attending the training and gaining technical knowledge shall be considered
as an asset. This would make you unique when compared with other individuals.
WHO CAN ATTEND
The training is specifically intended for individuals who are about complete Bachelor’s in
chemical engineering / students who are going to attend final year project work / who got
relieved in recent times from chemical engineering / experienced individuals who are willing to
gain technical knowledge and trying to swap from product to process engineering or technology
transfer / the one having trouble while performing detailed evaluation of ongoing processes or
any newly developed lab processes.
Session – 1 (2.5 hours + 0.5 hour Q&A) Session – 4 Continue….
4.2 Design of Heat exchanger
1.1 Introduction to Pharma,
4.3 Rate of Distillations
1.2 Basic Manufacturing operations
1.3 Basic Equipment in Pharma (API)
Session – 5 (2.5 hours + 0.5 hour Q&A)
1.4 Introduction to Batch processing &
Continuous processing Crystallization
1.4 Roles of Process Engineer in API Business. 5.1 Steps in Crystallization
(Lab Scale & Commercial Scale) 5.2 Types of crystallizations
Distillation
Session – 2 (2.5 hours + 0.5 hour Q&A) 5.3 Distillation Techniques
5.4 Scope of product yield/Process
2.1 API development Concept to
improvements
commercialization
2.1.1 Intellectual approvals
Session – 6 (2.5 hours + 0.5 hour Q&A)
2.1.2 Raw material CC calculations
2.1.3 Preparation of Gantt chart 6.1 Product capacity chart preparation
2.1.4 Basics of Lab development 6.2 Capacity enhancement & De-bottleneck of BCF
6.4 Overhead cost calculations
Session – 3 (2.5 hours + 0.5 hour Q&A)
Session – 7 (2.5 hours + 0.5 hour Q&A)
3.1 Basics of Process optimization
3.2 Process Validation at Lab scale, what-if, 7.1 Basic detailing of Process safety aspects
PDR, DOE, etc. 7.2 Preparation of HAZOP
3.2 Technology transfer 7.3 Investigation Tools & Methodologies
3.2.1 Equipment Selection criteria
3.2.2 Reaction Scale – up Session – 8 (2.5 hours + 0.5 hour Q&A)
Session – 4 (2.5 hours + 0.5 hour Q&A) 8.1 Capability analysis (Using Minitab)
8.2 Design of Experiments (Using Minitab)
3.2.3 Filtration Scale – up 8.3 Regulatory requirements of API
3.2.4 Types of drier and Scale – up 8.4 Outsourcing of intermediate stages
4.1 Utility calculations (heat load)
For registration, reach us at support@[Link]
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