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2026 |
2027 |
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Apr |
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Aug |
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A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
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Animal Health |
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3 |
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6 |
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A Practical Approach to Veterinary Vaccine Development and Registration in the EU
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Animal Health |
23-24 |
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9-10 |
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AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects
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Artificial Intelligence (AI) in Life Sciences |
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5 |
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10 |
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AI in Healthcare: Governance, Risk & Strategic Adoption
New for 2027
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Artificial Intelligence (AI) in Life Sciences |
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9 |
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APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence
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GxP |
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21-22 |
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28-29 |
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An Essential Overview of Medical Information
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Vigilance |
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3 |
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21 |
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An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices
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Medical Devices |
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9 |
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13 |
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An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals
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Medical Devices |
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19 |
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7 |
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An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices
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Medical Devices |
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19 |
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An Overview of EU and UK Regulatory Affairs
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0 |
21-22 |
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3-4 |
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Animal Feed and Feed Additive Registration in China and Thailand
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Animal Health |
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22 |
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15 |
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Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions
New for 2026
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0 |
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9 |
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9 |
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Biological Evaluation of Medical Devices
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Medical Devices |
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20-21 |
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1-2 |
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CAPA (Corrective and Preventative Action)
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0 |
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4 |
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14 |
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Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
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GxP |
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19-20 |
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22-23 |
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Cleanroom Requirements for Medical Device Manufacturers
New for 2026
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Medical Devices |
21 |
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22 |
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Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications
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0 |
30-1 |
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15-16 |
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Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness
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Clinical Research |
17-18 |
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15-16 |
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Clinical Trial Regulatory Requirements
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Clinical Research |
14-15 |
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1-2 |
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EU Pharmaceutical Regulations and Strategy
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0 |
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5-6 |
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1-2 |
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EU Proposed Pharmaceutical Legislation Changes
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0 |
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18 |
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7 |
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FDA Approval Process for Medical Devices
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Medical Devices |
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1-2 |
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24-25 |
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Global Market Access for Medical Device Software
New for 2026
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Medical Devices |
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30-1 |
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How the Pharmaceutical and Biotech Industries Work: From Molecule to Market
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0 |
28 |
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11 |
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Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
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Animal Health |
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15-16 |
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Masterclass: Market Authorisation of AI-enabled Medical Devices
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Artificial Intelligence (AI) in Life Sciences |
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8-9 |
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28-29 |
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Mastering CTD Submissions in the MENA Region
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0 |
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26 |
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25 |
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Mastering Computer System Validation
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GxP |
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10-11 |
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16-17 |
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Medical Device Cybersecurity and Regulatory Compliance
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Medical Devices |
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15-16 |
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18-19 |
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Medical Device Regulation in the Eurasian Union, Russia and the CIS
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Medical Devices |
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8-9 |
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29-30 |
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Medical Device Regulations in Asia-Pacific Markets
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Medical Devices |
16-17 |
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2-3 |
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Medical Device Regulations in the Middle East and North Africa
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Medical Devices |
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18-19 |
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17-18 |
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Medical Device Single Audit Programme (MDSAP)
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Medical Devices |
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25-26 |
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Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
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Medical Devices |
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25-29 |
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5-9 |
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Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass
Updated for 2026
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0 |
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4 |
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10 |
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Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests
New for 2026
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Medical Devices |
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9 |
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Non-Conformance and Corrective Action for Medical Device Manufacturers
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Medical Devices |
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10 |
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Orphan Drug Regulatory Masterclass: EU & US Insights
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0 |
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6 |
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3 |
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Pharmaceutical Regulatory Affairs in Africa
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0 |
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3-4 |
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Pharmaceutical Regulatory Affairs in Asia
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0 |
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20-22 |
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3-5 |
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Pharmaceutical Regulatory Affairs in China
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0 |
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25-26 |
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19-20 |
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Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS
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0 |
30-1 |
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4-5 |
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Pharmaceutical Regulatory Affairs in the Middle East
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0 |
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23-24 |
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Pharmaceutical Regulatory Affairs in the Middle East and North Africa
New for 2026
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0 |
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20-22 |
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7-9 |
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Registration of Veterinary Pharmaceuticals in China
New for 2026
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Animal Health |
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22 |
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15 |
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Regulatory Compliance and Safety Standards for Aesthetic Devices
New for 2026
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Cosmetics |
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4 |
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Sterilization of Medical Devices
|
Medical Devices |
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12-13 |
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22-23 |
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The 2024 EU AI Act
New for 2026
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Artificial Intelligence (AI) in Life Sciences |
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3 |
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22 |
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The Common Technical Document
|
GxP |
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21-22 |
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13-14 |
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The FDA Drug Approval Process
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0 |
24-25 |
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22-23 |
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The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
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0 |
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12-13 |
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19-20 |
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UK Conformity Assessed (UKCA) Marking for Medical Devices
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Medical Devices |
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21 |
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14 |
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US FDA - Understanding Key Factors When Working with the FDA
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Biopharma |
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25 |
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26 |
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Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers
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Medical Devices |
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30 |
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7 |
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Variations to Marketing Authorisations
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0 |
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11-12 |
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14-15 |
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Veterinary Pharmaceutical Submissions in the EU
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Animal Health |
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19-20 |
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17-18 |
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Writing Inspection-Ready SOPs: Best Practice for Compliance and Control
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0 |
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26 |
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6 |
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