FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More

FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More is a webinar that covers topics such as:

  • Responsibilities of manufactures and suppliers
  • Regulatory requirements for supplier qualification
  • What are the FDA’s expectations in regards to quality agreements?
  • Best practices for supplier selection, qualification and management
  • Best practices for a good quality agreement
  • What is meant by the title owner, contractor, adulterated drug, and the term manufacturing within the guidance?
  • Documentation requirements and audit trails
  • Supplier audits

FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More is intended for:

  • Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists
  • Quality Assurance/Quality Control Directors, Managers, and Specialists
  • Engineering/Development Directors, Managers, and Specialists
  • Purchasing/Materials Management Directors, Managers, and Specialists
  • Document Control Managers and Specialists

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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