PharmTech

Computerized System Descriptions–How Hard Can It Be?

System documentation should include a system description, history, validation information, and references, according to Siegfried Schmitt, Vice President, Technical at Parexel. Q. Some 10 years ago, ...
Yahoo Finance

Master Risk-Based Computer System Validation to Cut Implementation Time - 2 Day Online ...

Dublin, May 14, 2025 (GLOBE NEWSWIRE) -- The "Risk-based Computer System Validation; Reduce Costs and Avoid 483s (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering.
Pharmabiz

Guidelines on process and computer-based validation to drive future of pharma operations ...

Incorporating Q8, Q9, Q10 into good manufacturing practices (GMP), guidance on process validation, health based exposure limits covering cleaning validation and computerized system validation are the ...
信濃毎日新聞デジタル

AI機能実装PV System稼働後のGVPバリデーション手法の ...

「AI機能実装PV System稼働後のGVPバリデーション手法のコンサルティングサポート開始」 株式会社ヒロファーマコンサルティング®（本社：大阪府大阪市、代表取締役：集 弘就）は、「AI機能を搭載した適正基準対応バリデーションシステム及び方法」に ...
Yahoo Finance

Digital Validation Demystified | GAMP 5 2.0 and CSA Integration Course - Master 21 CFR Part ...

Dublin, Aug. 25, 2025 (GLOBE NEWSWIRE) -- The "Digital Validation Demystified - GAMP? 5 2.0 and CSA Integration" training has been added to ResearchAndMarkets.com's offering. This course equips you ...