Registration for Fall 2026 programs and courses is now open. Learn more about the academic programs we are delivering in Fall 2026. If you have any questions about part-time studies, please contact us.
Good documentation constitutes an essential part of the effective pharmaceutical quality system. During their inspections of manufacturing sites, regulatory inspectors often spend much time examining a company's documents and records. This workshop focuses on the GMP requirements for documentation and records, types of documents needed in pharmaceutical industries and record retention and keeping practices.
This workshop is recommended for individuals needing additional expertise in developing, implementing, and managing documentation systems at pharmaceutical manufacturing sites.
Ancillary fees will be added at checkout and will vary based on the number of courses selected. For details on how the fees are calculated, please refer to ancillary fees for part-time studies.