Upcoming Courses

• Bratislava, Slovakia, Sep 21, 2026
• Online Attendance, Organizated by Fleming
• The Legacy Wells and CCS Conference is an advanced training event focused on Carbon Capture Utilization and Storage CCUS, well integrity, carbon storage safety, and risk management. Attendees will gain practical insights into CO2 storage, leak prevention, corrosion management, carbon sequestration, and sustainable energy solutions through expert led sessions and real world case studies.

• Bratislava - Raca, Slovakia, Sep 23, 2026
• Online Attendance, Organizated by Fleming
• This live online training course provides practical insights into immunogenicity assessment, anti-drug antibodies (ADA), bioanalytical methods, regulatory requirements, and risk mitigation strategies for biologics, biopharmaceuticals, biosimilars, vaccines, and ATMPs. Led by renowned industry experts, participants will explore preclinical and clinical considerations, assay development, quality control, and global regulatory expectations.

• Bratislava, Slovakia, Oct 19, 2026
• Online Attendance, Organizated by Fleming
• Discover how Artificial Intelligence is transforming pharmacovigilance through expert-led training on AI governance, regulatory compliance, signal detection, validation, risk management, and digital transformation. Gain practical insights from real-world case studies, interactive sessions, and industry best practices to implement AI responsibly in regulated drug safety environments.

• Basel, Switzerland, Oct 20, 2026
• Mixed Attendance, Organizated by Fleming
• The Drug-Device Combination Products Masterclass 2026 is an advanced training program designed for professionals working in pharmaceuticals, biotechnology, biologics, and medical devices. Led by industry expert Abha Raveau-Violette, the course covers regulatory frameworks, FDA requirements, EU MDR Article 117, design controls, risk management, human factors, manufacturing, and global approval strategies.

• Bratislava, Slovakia, Nov 04, 2026
• Online Attendance, Organizated by Fleming
• Enhance your expertise in CMC requirements for generic drug applications through expert-led training covering CTD Module 3, API and drug product dossiers, DMFs, ASMFs, process validation, regulatory compliance, and the latest ICH, EMA, and FDA guidelines.