Join the Stability & Shelf Life of Biologics training on 27–28 October 2026 in Rome and online. Learn practical approaches to stability studies, shelf-life justification, cold chain management, and global regulatory expectations for biologics.

Fleming Events presents Monoclonal Antibodies – Quality & Regulatory Requirements on 13–14 October 2026 in Vienna and online. Gain practical insights into CMC, ICH guidelines, analytical development, process validation, and lifecycle management.

Fleming will host Monoclonal Antibodies – Quality & Regulatory Requirements on 13–14 October 2026 in Vienna and online. The training explores ICH guidelines, comparability, CMC, analytics, lifecycle management and regulatory strategies for mAbs.

Fleming’s masterclass in Basel on Oct 20–21, 2026, explores design controls, regulatory submissions, and global approval strategies for drug‑device combination products.

Join Advanced GCP in Action to gain practical insights into GCP compliance, clinical trial audits, inspections, data integrity, risk-based monitoring, and regulatory expectations from industry experts.