CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture

CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture is an online event dedicated to a contract between a GMP Contract Manufacturer and a pharmaceutical firm is a Quality Agreement .

CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture covers topics such as:

  • What a Quality Agreement is and isn’t?
  • The Who and What of a good Quality Agreement
  • GMP responsibilities
  • Responsibilities of the owner vs. contract facility
  • A comparison of the new guidelines from the FDA and the EU

CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture intended for:

  • External Manufacturing / Outsourcing Departments
  • Quality Assurance Departments
  • Technology Transfer Departments
  • Quality Auditing Departments
  • Supply Chain Departments
  • Regulatory Affairs / Compliance Departments
  • Risk Management Departments
  • Purchasing Departments

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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