Dublin, Nov. 10, 2026 (GLOBE NEWSWIRE) -- "Mastering Aseptic Processing for Pharmaceutical & Biotech Manufacturing (Mar 24th - Mar 25th, 2026)" has been added to ResearchAndMarkets.com's offering.
Research and Markets has made the recording of “Mastering Aseptic Processing for Pharmaceutical & Biotech Manufacturing” available for on-demand purchase. The two-day virtual course, led by Dr. Barry A. Friedman, was held live on March 24-25, 2026. It covers the critical factors manufacturers need to control to keep sterile production compliant, from contamination sources and cleaning to media fill design and FDA inspection findings.
The course is pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for up to 7.0 credits toward Regulatory Affairs Certification (RAC) recertification on full completion.
Key Event Facts
- Course: Mastering Aseptic Processing for Pharmaceutical & Biotech Manufacturing
- Format: Recorded training, accessed online through a secure website
- Original live event: March 24-25, 2026 (EST)
- Duration: Two days
- Continuing education: Pre-approved by RAPS for up to 7.0 RAC recertification credits
- Speaker: Dr. Barry A. Friedman
What the Course Covers
The programme opens with an introduction to aseptic processing. It then examines contamination sources in sterile manufacturing, cross-contamination hazards and endotoxin sources. Participants review cleaning processes and agents for sterile production, equipment set-up and sterilization processes. They also look at developing procedures for processes, preventive maintenance and corrective and preventive action (CAPA).
A central focus is media fills: how to develop media fill requirements in an aseptic environment and how to design simulations around worst-case scenarios. The course also covers smoke studies and their role in aseptic production in ISO Class 5 facilities, personnel training including gowning, and Form FDA 483 observations.
Why You Should Watch
- Develop media fill requirements and simulations built around worst-case scenarios
- Apply smoke studies to aseptic production in ISO Class 5 facilities
- Identify contamination, cross-contamination and endotoxin sources in sterile manufacturing
- Strengthen cleaning, sterilization, equipment set-up and gowning practices
- Learn from Form FDA 483 observations, and earn up to 7.0 RAPS credits toward RAC recertification
Who Should Watch
The course is designed for:
- Manufacturing and quality control professionals
- Project managers
- Formulation developers
- Process chemistry specialists
- Analytical chemists
- In-house regulatory compliance officials
- Scale-up and technology transfer professionals
- Validation experts
Featured Speaker
- Dr. Barry A. Friedman
Pharmaceutical and biotech manufacturing professionals who want to strengthen aseptic processing compliance can purchase the recording through Research and Markets. Access details are sent by email.
For more information about this training visit https://www.researchandmarkets.com/r/omjnku
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