Book Online Tickets for Process and Cleaning Validation Workshop, Hyderabad.  This interactive 2 day Live In Person seminar on Process and Cleaning Validation, utilizes the: – Product and process Realization using current cGMP requirements, Concepts and Principles of – Product and process Realization usi

Process and Cleaning Validation Workshop

 

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About The Event

 This interactive 2 day Live In Person seminar on Process and Cleaning Validation, utilizes the: – Product and process Realization using current cGMP requirements, Concepts and Principles of – Product and process Realization using Quality by Design, Risk based approach with Illustrative Example as the basis for explaining and providing examples of how products and processes can be validated, using QRM with special emphasis on the considerations for implementing these processes in manufacturing with respect to Formulation and API.

 

WHO SHOULD ATTEND:
A must attend seminar for professionals in Pharmaceuticals, QC Laboratories, Manufacturers of drug substances (APIs), Oral Solid Dosage Form, Contract Laboratories, Clinical research Organizations, Contract Research Organisations, Contract Manufacturing Organisations and Biopharma companies.
DEPARTMENTS:
– Quality Control
– Quality Assurance
– Research and Development
– Manufacturing
– Engineering
– Analytical Development Laboratories
– Regulatory Compliance
– Validation
– Production
– Technology Transfer
– Laboratory
– Documentation
– Training Departments
PROFESSIONALS:
– Managers
– Supervisors
– Senior Managers
– Team Leaders
– Executives and Senior Executives
– General Managers
– Engineers
– Design Engineers
– Plant Managers
– Laboratory Managers and Supervisors
– Regulatory Affairs Managers
– Documentation Specialists & Analysts
– Internal and External Auditors

 

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