In September, the FDA published Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients to provide API manufacturers with recommendations intended to ensure compliance with regulations.

What is in the new FDA Guidance:

This guidance document, originally published by ICH in 2000, includes recommended best practices for computer systems, such as:

  • Validation
  • System documentation
  • Security
  • Record protection and retention
  • Audit trails
  • SOPs for system use and support
  • Change management
  • Incident investigation

Do you need more help implementing these recommendations in your organization? Talk to our CSV experts about how you can update your practices for compliance.

 
Like it? Share it:

You may also like

Are you prepared for WHO draft guidance on Good Data and Record Management Practices?
5 October, 2015

In September 2015, the World Health Organization (WHO) published a draft guidance document focused solely on data integr...

Are your procedures aligned with the FDA Guidance for Analytical Procedures and Methods Validation?
7 August, 2015

Last month, the FDA published this document for drug and biological license applicants submitting analytical procedures ...

23 Data Integrity FAQs Answered By The EMA
22 September, 2016

Last month, the EMA’s Good Manufacturing Practice (GMP) / Good Distribution Practice (GDP) Inspectors Working Group publ...