No pharmaceutical product reaches a patient without protection against contamination. For many sterile products, this means full aseptic manufacturing. But sterility is fragile. Microorganisms and ...

Environmental monitoring (EM) is the backbone of cleanroom control in pharmaceutical manufacturing. For lab managers, QA/QC leads, and scientific staff, it ensures that the environment where products ...

Muscat: The Public Authority for Special Economic Zones and Free Zones (Opaz), represented by the Compliance and Environmental Affairs Department, organised a workshop on general environmental ...

As Advanced Therapeutic Medicinal Products (ATMPs) surge in popularity and the market sees an increase in therapy development and available products, contemporary manufacturing processes must align ...

Editor’s note: This article is the third in a series to help practitioners learn about the AICPA’s new quality management standards and prepare to implement them. The new final standards on quality ...