05.08.25 -- Navigating Tariffs: Implications And Strategies For Pharmaceuticals Manufacturers

As the industry continues its move toward biologics, innovative solutions and technologies will be needed to ensure a safe and reliable approach to the manufacturing and delivery of these drugs.

Discover how a robust Quality Management System can help your organization reduce the cost of poor quality while maintaining high standards and enhancing customer satisfaction.

One way to address risk related to product quality is by implementing a Question-Based Review approach. Read on to learn about this approach and its advantages.

This discussion explores critical aspects of maintaining sterility in pharmaceutical manufacturing, from facility design and environmental monitoring to regulatory compliance and common misconceptions.

Multi-shaft mixers are versatile systems used in the production of pharma and medical products. Here, we discuss equipment features commonly supplied on multi-shaft mixers for sanitary applications.

Review the complexities of developing linkers – chemical moieties which attach a drug payload to an antibody – and considerations when identifying a CRO for ADC research and development.

There are two basic models of pharma manufacturing: batch and continuous. Delve in as we compare the two and examine the challenges they bring to containment product design.

Compressed tablets are common oral solid dosages that contain the API and various excipients. Learn about the critical steps in selecting manufacturing methods to achieve the desired therapeutic effects.

Bovine collagen, valued for biocompatibility and versatility, is gaining attention for medical devices in China as regulatory barriers ease, though safety assurances remain crucial.

Leveraging the expertise and experience of a trusted partner can reduce risk and accelerate the time to market for drug-device combination products by creating an optimal Validation Master Plan.