SGS Pharma Webinars

Join us to explore best-practice strategies and technologies that strengthen end-to-end antibody‑drug conjugate (ADC) development workflows.

Learn how a modern CHIM approach, Antwerp’s integrated setup and Belgium’s faster timeline, can give you the early efficacy signals your investors trust

Learn how chemical challenge agents work, when to apply them and how SGS’ proven approach helps pharma and biotech teams.

Join our live expert roundtable on USP 665 compliance and E&L challenges in the (bio)pharmaceutical industry.

Join us for an in-depth webinar designed for professionals involved in the development, validation and regulatory submission of in vitro diagnostic (IVD) devices.

Join our expert-led webinar to explore nitrosamine risks, testing strategies and mitigation approaches to safeguard patients and ensure compliance.

Join our expert-led webinar to gain a clear understanding of the Notification of Changes (NoC) process, including the updated submission flowchart and documentation requirements.

Join our webinar to hear further insights into ICH E6 R3 from our experts

Join our webinar for an overview of the new requirements, the state of the art, the risks and benefits and how to demonstrate clinical performance.

This webinar will provide an overview of the QMS audit process under the IVDR and share practical guidance to help manufacturers prepare effectively.