Farah Nadeem

  • Next: 11-12 Jul 2024 Live online
  • Also: 11-12 Nov 2024 Live online

Stability Testing of Pharmaceuticals and Biopharmaceuticals

Live online

Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learn how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.

  • 12 CPD hours Focused
  • Presented by Farah Nadeem
  • Next: 17-18 Jul 2024 Live online
  • Also: 18-19 Nov 2024 Live online

Understanding Active Pharmaceutical Ingredients (APIs)

Live online

This course has been designed to provide attendees with a fundamental understanding of best practice and the regulatory environment applicable to active pharmaceutical ingredients in the pharmaceutical industry. It will cover key terminology, the EU and USA regulatory framework, Good Manufacturing Practice (GMP) requirements including controls and validation, and consider Good Distribution Practice (GDP) and how to manage your supply chain.

  • 12 CPD hours Focused
  • Presented by Farah Nadeem
  • Next: 24-25 Jul 2024 Live online
  • Also: 25-26 Nov 2024 Live online

Understanding Computer System Validation (CSV)

Live online

This course covers the key concepts of computer systems validation and provides practical guidance on how to comply with the regulations applicable to the pharmaceutical industry. It will include the regulatory requirements, the industry standards and best industry practice based on Good Automated Machine Practice (GAMPĀ®5). It will provide a practical and efficient framework for computerised systems validation and compliance, and gives attendees an appreciation of how these ideas may be applied to their own systems and processes.

  • 12 CPD hours Focused
  • Presented by Farah Nadeem