Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices 2018

  • 10 Jul 2018
  • Webinar

Description

Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices 2018 is an event dedicated to learn how to develop compliant validation protocol and analytical procedures as per FDA and USP guidance.

Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices 2018 covers topics such as:

  • Familiarize with FDA requirements of analytical procedures
  • Discuss GMP regulatory requirements for Analytical Test Methods
  • Understand USP Good Documentation Practices
  • Development of method validation protocols
  • Establish acceptance criteria for validation
  • Discuss lifecycle management of method validation

Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices 2018 intended for:

  • QA and QC Managers
  • R&D Analysts
  • Directors
  • Regulatory Scientists
  • Manufacturers
  • Regulators
  • Quality Managers and Personnel
  • Laboratory Managers
  • Regulatory Affairs

Past Events

Important

Please, check "Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Management, Quality assurance
Health & Medicine: Healthcare, Medical laboratories, Pharma
Science: Biochemistry, Chemistry, Health sciences, Laboratories, Life Sciences & Biology
Technology: Biotechnology

Other Events with Similar Categories

Other Events with Similar Location or Organizer

Featured Conferences & Exhibitions