RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance 2012

  • 18-20 Jun 2012
  • Mumbai, India

Description

RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance 2012 is a seminar that covers topics such as:

  • Laws and Regulations in the U.S
  • Introduction to U.S. Drug Regulation
  • Violations and Responses
  • The U.S. Drug GMP
  • An Overview of ICH Q8, Q9, and Q10
  • Filings and Submissions - DMF and Clinical Trials
  • Biosimilars in the U.S., An Overview
  • Risk Analysis and Corrective and Preventive Actions (CAPA)
  • Process Validation

RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance 2012 brings together Vice Presidents of Technical Departments, Presidents, Directors, Managers, Quality, Regulatory Associates and Analysts, Research, Regulatory and Development Group Heads.

Past Events

Important

Please, check "RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma

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