QRM Based Integrated C&Q Series - Implementing a Science and Risk Based Approach to Commissioning & Qualification Complimentary Learning Level: Intermediate Session Length: 2 hours This webinar is the first in a series...
Holistic Pharma 4.0 Digital Maturity Assessment Complimentary Learning Level: Basic Session Length: 1.5 hours The pharmaceutical industry is highly regulated due to its involvement with products that are essential to...
CSV vs CSA: GAMP 5's Actionable Steps to Transitioning Your Validation Complimentary Learning Level: Intermediate Session Length: 1 hour CSV or CSA? Some companies are still debating which approach is right for them and...
Actively Identifying Limiting Factors in Speed to Launch Drug Products Complimentary Learning Level: Advanced Session Length: 1.5 hour In the dynamic landscape of drug manufacturing, the development and launch of...
Secrets in the Digital Transformation Vibe Powered and Led by Women in Pharma ® This session features a comprehensive discussion on the impact of digital transformation in the pharmaceutical and biotech industries. It...
Improved Data Integrity via Digitization of Environmental Monitoring Complimentary Learning Level: Intermediate Session Length: 1 hour In today’s pharmaceutical industry there is myriad of GMP data being generated in the...
Purified Water Microbial Testing: False OOS Due to TNTC vs Filtration Volume Complimentary Learning Level: Advanced Session Length: 1 hour Due to filtering 100 ml of purified water through 47mm membrane filter there is a...
Quality Culture Matters: Key to Unlocking the Digital Validation Power Extended Learning Learning Level: Intermediate Session Length: 1 hour The forthcoming ISPE Good Practice Guide: Digital Validation emphasizes that a...
Using Simulations to Accelerate Pharmaceutical Manufacturing Processes Extended Learning Learning Level: Basic Session Length: 1 hour The pharmaceutical industry faces diverse challenges, ranging from drug delivery to...
