BIA Events

Jumpstart your career in regulatory affairs with our Overview of EU Pharmaceutical Regulatory Affairs training course.

The Global Cell & Gene Therapy Summit creates an ideal environment for researchers, clinicians, industry professionals, and stakeholders to remain abreast of the latest advancements in cell & gene therapy.

Join Founders Growth Community x Innovate Cambridge for our monthly drop in and networking event!

Join us for an evening of insightful panel discussion with experts in tax, law, executive search, leadership and organization development to answer this pivotal question. This is a unique opportunity to connect with industry leaders, exchange innovative ideas and insights, and forge valuable relationships within the UK's life science and technology sectors.

Join the Precision Clinical Trials Summit Boston 2025 to explore cutting-edge advancements, network with experts, and shape the future of clinical research.

Advanced Therapies Integrates North is dedicated to uniting industry leaders to drive and realize the full potential of Advanced Therapies and Medicinal Products (ATMPs).

Save the date for SynBioBeta 2025: The Global Synthetic Biology Conference, taking place from May 5-8, 2025, in the heart of California's Silicon Valley, San Jose.

Discover how to successfully complete your projects with our skills-based ‘Project Management for Regulatory Affairs Professionals’ CRED course.

CDMO Live 2025 is an exclusive event designed to spotlight the pivotal role of outsourcing in pharma and biotech and to connect partners. Attendees will gain valuable insights into how to accelerate drug development and manufacturing, de-carbonise by reducing Scope 3 emissions, and optimise contract manufacturing networks for operational efficiencies, resilience, and quality. Find you next partner with PartnerMatch, our 1-2-1 curated meeting programme that connect sponsors with relevant partners who can help them with drug development and manufacturing.

Biopharmaceutical process development faces new challenges: shorter time-to-market and changing regulatory expectations for new molecular entities. Implementing tools and solutions are essential for optimizing manufacturing workflows that are scalable, flexible, and transferable.