Summary : This series of webinars, available on-demand, provides a comprehensive overview of the proposed changes to Annex 1, the EU's guidance on manufacturing sterile medicinal products. more...

Summary : Updated for 2020, this 3 day course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA. more...

Summary : COURSE DESCRIPTION   OVERVIEW   Have you ever had a deviation occur that forced you to retrain staff, had a similar deviation appear, then correct it with another round of the same training on the same more...

Summary : FREE to current Pharmig Industry / NHS / and Supplier Members Nominal Fees for all Non-Members Technical presentations from leading supplier experts   Agenda (GMT time zone)   12.20 – 12.30  Welcome more...

Summary : This course is a comprehensive review of the philosophies and requirements of ISO/IEC 17025:2017.  The participant will gain an understanding of conformity assessment using the risks and opportunities-based approach.   This more...

Summary : Those concerned with the control of endotoxins, administration of deviations/root cause analysis, batch release, and audits and inspections will want to join this webinar to learn about the content of the new guideline.  more...

Summary : COURSE DESCRIPTION OVERVIEW   Method validation is legally required to show regulatory authorities that your organization’s method is appropriate for its intended use.  If not performed properly, method validation more...

Summary : Labs still using paper, spreadsheets and other legacy systems for their environmental monitoring are open to a range of risks, which could have heavy consequences.   Join Andrew Davies, Microgenetics Managing Director, on more...