Continuing Professional Development  

Industrial Pharmacy is one of the backbones of Life-Science, where life-saving medicines are formulated.


Needless to say, the Pharmacists and Science graduates who are involved in formulating such life-saving medicines MUST possess adequate knowledge and skills in order to perform their professional duties. In addition to that, they need to be continuously updating their Knowledge about the industry, owing to constant changes in regulatory requirements. Failure to do so would render them "out of place". 


And as for the fresh graduates, though they would have enough theoretical knowledge about the various aspects of Pharmaceutical Sciences, what they might lack is the applicability in the industry and the skills that are needed to utilise their knowledge in their respective job functions.


This gap is what makes them an average professional.   

How do we bridge this gap?

No worries. Through our signature program called PerPharm, we simply bridge this gap


In short, we bring out the PERfection in each PHARMaceutical professional, in order to make them PERform to the fullest of their ability.


C Level

The Beginners

Objective – to make them confident of attending job interviews and become competent to handle the job.

Departments – Manufacturing & Packaging, QA, RA, QC, Product development, Warehouse & Project Engineering.

  • Day-1 Pharmaceutical facility – introduction, various departments & it’s activities

  • Day-2 Good Manufacturing Practices & Documentation

  • Day-3 Various regulatory bodies; inspections

  • Day-4 Attending interviews; mock interviews

  • Day-5 Facility visit

B Level

The Juniors

Objective – to make them conversant & confident to handle the job.

Departments – Manufacturing & Packaging, QA, RA, QC, Product development, Warehouse & Project Engineering.

  • Day-1 Regulatory bodies – introduction

  • Day-2 GMP guidelines, Part-1

  • Day-3 GMP guidelines, Part-2

  • Day-4 Handling regulatory inspections

  • Day-5 Practical workshop

A Level

The Seniors

Objective – to make them confident to face regulatory inspections.

Departments – Manufacturing & Packaging, QA, RA, QC, Warehouse & Engineering.

  • Day-1 EU-GMP guidelines

  • Day-2 Written Exam

  • Day-3 Mock Inspections

Besides the above modules, we have designed several 1-day, 2-day and 3-day training courses on various topics ranging from Auditing techniques, Audit report writing, Cleaning Validation, Data Integrity, Environmental Monitoring, Facility Design, Failure Investigation, Good Manufacturing Practices (GMP), Good Automated Manufacturing Practices (GAMP), Heating Ventilation & Air Conditioning (HVAC), Microbiological techniques, Plant Qualifications, Purified Water system, Quality Risk Management (QRM) and many more.

Plans are underway to introduce Quality Management System (QMS) Lead Auditor course.

Plans are also underway to introduce online courses.

Meet our Faculty

Head Trainer

HR & Admin  

Communication trainer

QA & Regulatory Affairs


QA & Microbiology

How we do this?

We have designed three levels of training modules


Contact us and discover how we can transform you/ your employees.


The training programs happen in London and few major cities in India, viz., Ahmedabad, Bengaluru, Chennai, Hyderabad, Mumbai and Panjim (Goa). Besides these venues, we can organise programs at clients premises as well. 

Please send your inquiry through email.

While sending an inquiry, please send your CV and preferred location of training. We will then recommend the suitable level of training along with optional training time-slots. You can choose the time-slot that is convenient to you.


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