3/5付のMED DEVICE ONLINEがEU-GMP Annex 1関連の抄録を掲載しています。
ご存じの通り、「EU-GMP Annex 1 ≒ PIC/S GMP Annex 1」です。
企業による宣伝の一環としての抄録ではありますが、関係者および興味のある方は、下記URLsの抄録を参照ください。
3/5付「Most Frequently Asked Questions On The Revised EU GMP Annex 1: Volume 1」
https://www.meddeviceonline.com/doc/most-frequently-asked-questions-on-the-revised-eu-gmp-annex-volume-one-0001
3/5付「Most Frequently Asked Questions On The Revised EU GMP Annex 1: Volume 2」
https://www.meddeviceonline.com/doc/most-frequently-asked-questions-on-the-revised-eu-gmp-annex-volume-two-0001
3/4付「Achieving EU GMP Annex 1 Compliance Through An End-To-End Approach To Contamination Control」
https://www.meddeviceonline.com/doc/achieving-eu-gmp-annex-compliance-through-an-end-to-end-approach-to-contamination-control-0001
Case Study「Meeting Annex 1 Regulations: A Proactive Approach To Regulatory Compliance」
https://www.meddeviceonline.com/doc/meeting-annex-regulations-a-proactive-approach-to-regulatory-compliance-0001
3/13付「Managing Risks In Injectable Drug Delivery: Solutions For Today's Drug Products And Tomorrow's Novel Applications」
https://www.meddeviceonline.com/doc/managing-risks-in-injectable-drug-delivery-solutions-for-today-s-drug-products-and-tomorrow-s-novel-applications-0001
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