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.
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How to overcome this gap?
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No worries. Through our signature program called PharmXceed, we simply bridge this gap.
In short, we bring out the perfection in each Pharmaceutical professional, in order to make them exceed the expectations of the industrial sector.
C Level
The Beginners
Objective – to make them conversant with their job functions.
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Departments – Manufacturing & Packaging, QA, RA, QC, Product development, Warehouse & Project Engineering.
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Day-1 Pharmaceutical facility – introduction, various departments & it’s activities, Good Manufacturing Practices, Documentation & Data Integrity.
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Day-2 Introduction to various regulatory bodies & inspections.
B Level
The Juniors
Objective – to make them conversant with regulatory requirements.
Departments – Manufacturing & Packaging, QA, RA, QC, Product development, Warehouse & Project Engineering.
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Day-1 Introduction to various Regulatory bodies. EU-GMP guidelines.
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Day-2 Mock audits - as Internal Auditor; Handling regulatory inspections. Practical workshop, Q&As and Discussions
A Level
The Seniors
Objective – to make them confident to face regulatory inspections.
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Departments – Manufacturing & Packaging, QA, RA, QC, Warehouse & Engineering.
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Day-1 Orange Guide, EU-GMP guidelines.
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Day-2 Mock Inspections - as Lead Auditor in a group of 2-3 associate auditors. Written Exam & Open discussions.
Besides the above modules, we have designed several 1-day training courses on various topics ranging from Auditing techniques, Audit report writing, Cleaning Validation, Data Integrity, Environmental Monitoring, 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.
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Plans are underway to introduce remote (online) courses.
Meet our faculty
ram iyer
Principal Consultant
Expert in the areas of Qualifications, Process & Cleaning Validation,
Water system, Change Control, etc.
semerab tewolde
Qualified Person (QP)
Medical Doctor and Qualified Person in the UK. Expert in QMS documentation & Data integrity.
nandita iyer
Quality Assurance
Expert in SOP writing, QMS Document controls, Environmental monitoring, etc.
pavithra iyer
Communication Trainer
Expert in training people in English language & Communication skills, helping them to overcome fear and instill self-confidence.
How we do this?
We have designed three levels of training modules
NOTE:
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The training programs happen at the following locations,
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INDIA
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Ahmedabad
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Bengaluru
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Chennai
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Goa
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Hyderabad
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Mumbai
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UK
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London
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Besides these venues, we can organise programs at clients premises as well (minimum number of participants should be 10).
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Please send your inquiry through email.
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Individual enquiries - 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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Corporate enquiries - please send the list of employees, along with their job title and the departments in which each employee works.