The following guideline can be ordered through the address listed in the "Source/Publisher"-category. In cases in which you can order through the Internet we have established a hyperlink.

FA Guidance for Industry: Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Annex



This Annex document is intended to be considered in conjunction with the ICH Q12 Core Guideline being simultaneously published for comment

Go back

GMP Conferences by Topics