Overview Level: Intermediate Type: Certificate ISPE Continuing Education Units (CEUs): 2.8 ISPE’s Good Engineering Practices certificate program is a comprehensive program designed to equip professionals with the knowledge and skills required to...
ISPE Clinical Supply Business Continuity Survey Results and Discussion Complimentary Learning Level: Intermediate Time: 1000 - 1100 EST Session Length: 1 hour ISPE Clinical Supply Business Continuity Survey was conducted in November 2025. This...
QRM Based Integrated C&Q Series—System Boundaries and System Classification Complimentary Learning Level: Intermediate Time: 1000 - 1130 EST Session Length: 1.5 hour This is the sixth webinar in the C&Q CoP ten-part webinar series. System boundary...
SAVE THE DATE ISPE ANNEX 1 SYMPOSIUM in collaborazione con ISPE DACH | France | Ireland | Nordic Affiliates 29-30 Settembre 2025 Ospedale degli Innocenti Piazza della SS. Annunziata, 12 50121, Firenze Per la prima volta in Italia cinque Affiliate...
We’re excited to invite you to the Essential Innovations Event, a dynamic day of discussion, discovery, and real-world insights into cutting-edge innovation in the life sciences sector. 📍 Location: Charleville Park Hotel (Morning) + BCD Cork Site...
Women in Pharma Event: Work Life Balance: How do you manage it? Thursday, June 5, 2025 5:30 pm - 8:30 pm Hopewell Valley Vineyards 46 Yard Rd Pennington, NJ 08534 Join us for an honest, inspiring, and thought-provoking panel discussion featuring...
GAMP CoP "GAMP and ISA 95" Chris Monchinski, chair of the ISA-95 Standard Committee, will present on the important relationship between the ISA-95 Standard on integration between the business systems (ERP) and the control systems and the strong...
Ethylene oxide (EtO) gas sterilization is used across the pharma industry for a variety of products, including but not limited to medical devices. In light of FDA news release of January 2024, which encouraged end users to seek alternative...
Life Cycle Approach to Process Validation- Stage 3 Implementation Complimentary Learning Level: Intermediate Time: 1100 - 1200 EST Session Length: 1 hour Process validation is a fundamental requirement in pharmaceutical manufacturing, ensuring that...
Join us on June, 19th at UCB, Anderlecht (BE), for an exciting GAMP event on the " validation of SaaS systems”. Learn from experts in the field in how to manage SaaS vendors and what measures you can take to ensure a SaaS system is maintained in a...
