Professionals across the pharmaceutical and medical device industries are invited to attend an upcoming webinar that promises to provide a comprehensive overview of the international standards shaping syringe testing. The session will explore the technical intricacies of testing requirements, from the syringe's subassembly components to their performance in prefilled configurations.

The webinar will take participants through the evolving expectations for syringe testing across the entire value chain—from original equipment manufacturers (OEMs) to Contract Development and Manufacturing Organizations (CDMOs) responsible for fill-finish operations. Attendees will gain valuable insight into the nuances of how testing evolves as products move closer to patient-ready use.

One of the key features of the webinar is an in-depth discussion of individual test methods. Experts will share best practices for equipment setup and data analysis, offering practical guidance tailored to different laboratory environments. The session will highlight strategies for configuring equipment to reduce setup time while ensuring compatibility with a wide range of syringe formats.

Participants can expect to leave with a clearer understanding of:

• The components of syringes and the testing protocols required for each part
• How to match syringe styles and use cases with the appropriate international standards
• Methods for interpreting complex references and equivalencies among various regulatory guidelines
• Approaches to streamline lab operations and ensure consistent, reliable testing outcomes

This educational event is especially relevant for professionals involved in quality assurance, regulatory affairs, laboratory management, and syringe design or manufacturing. Whether you're navigating ISO standards or working on the front lines of fill-finish operations, the webinar aims to equip you with the tools and insights needed to optimize testing workflows and ensure compliance.

View 25 Ways to Test a Syringe now