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Live online
Classroom
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2026 |
2027 |
| Mar |
Apr |
May |
Jun |
Jul |
Aug |
Sep |
Oct |
Nov |
Dec |
Jan |
Feb |
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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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7 |
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3 |
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A Practical Approach to Veterinary Vaccine Development and Registration in the EU
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Animal Health |
10-11 |
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23-24 |
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A Practical Guide to Producing and Maintaining the PSMF
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Vigilance |
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16 |
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A Practical Guide to Writing Risk Management Plans (RMPs)
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Vigilance |
20 |
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19 |
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A Practical Introduction to Good Clinical Practice (GCP)
New for 2026
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GxP |
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15 |
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6 |
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A Practical Overview of Pre-Filled Syringes
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Medical Devices |
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11-12 |
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11-12 |
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A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK
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Medical Devices |
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29 |
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20 |
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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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11 |
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5 |
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AI in Healthcare: Governance, Risk & Strategic Adoption
New for 2026
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Artificial Intelligence (AI) in Life Sciences |
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22 |
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AI in Pharmacovigilance
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Artificial Intelligence (AI) in Life Sciences |
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18 |
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18 |
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APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence
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GxP |
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29-30 |
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21-22 |
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Achieving Publication Success in Scientific Journals
New for 2026
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Medical Writing |
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21 |
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Additional Risk Minimization Measures (aRMMs) and Their Effectiveness
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Vigilance |
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16 |
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2 |
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Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider
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Vigilance |
23-25 |
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21-25 |
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Advanced Veterinary Pharmacovigilance
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Animal Health |
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11-12 |
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4-5 |
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An Essential Overview of Medical Information
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Regulatory Affairs |
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22 |
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3 |
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An Essential Overview of the Pharmaceutical and Biotech Industries
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Regulatory Affairs |
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28 |
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An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices
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Medical Devices |
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14 |
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9 |
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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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8 |
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19 |
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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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21 |
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19 |
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An Introduction to Signal Detection
New for 2026
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Vigilance |
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16 |
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14 |
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An Introduction to Technology Transfer for Solid Dosage Forms
New for 2026
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GxP |
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18 |
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An Introduction to the Design and Development of Medical Devices
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Medical Devices |
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29-30 |
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9-10 |
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An Overview of EU and UK Regulatory Affairs
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Regulatory Affairs |
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21-22 |
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An Overview of Ethical Standards in Clinical Research Publication
New for 2026
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GxP |
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13 |
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11 |
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An introduction to Risk Management ISO 14971:2019
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Medical Devices |
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27 |
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20 |
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Animal Feed and Feed Additive Registration in China and Thailand
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Animal Health |
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16 |
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22 |
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Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions
New for 2026
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Regulatory Affairs |
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10 |
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9 |
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Behavioural Risk Management in Clinical Trials
New for 2026
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Clinical Research |
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13 |
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5 |
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Best Practices for Supplier Qualification in Life Science
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Medical Devices |
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6-7 |
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12-13 |
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Biological Evaluation of Medical Devices
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Medical Devices |
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13-14 |
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Biosimilars
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Biopharma |
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22-23 |
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Biotechnology for the Non-Biotechnologist
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Biopharma |
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10-12 |
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30-4 |
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Building The Business Case For Pharma 4.0
New for 2026
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Medical Technology |
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13 |
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6 |
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CAPA (Corrective and Preventative Action)
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Regulatory Affairs |
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15 |
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4 |
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Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
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GxP |
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23-24 |
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19-20 |
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Cleaning Validation - Best Practice in Pharmaceuticals
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GxP |
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23-24 |
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1-2 |
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Cleanroom Requirements for Medical Device Manufacturers
New for 2026
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Medical Devices |
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21 |
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Clinical & Post-Marketing Safety
New for 2026
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Vigilance |
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11-12 |
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16-17 |
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Clinical Evaluation of Medical Device Software and Software as a Medical Device
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Medical Devices |
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28 |
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1 |
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Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
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Regulatory Affairs |
16-17 |
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30-1 |
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Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness
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Clinical Research |
23-24 |
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17-18 |
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Clinical Research Project Management
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Medical Devices |
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29-1 |
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21-23 |
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Clinical Trial Agreements: Key Legal, Regulatory and IP Considerations for the EU and UK Markets
New for 2026
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Commercial Contracts |
18 |
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2 |
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24 |
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Clinical Trial Monitoring
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Clinical Research |
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18-19 |
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10-11 |
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Clinical Trial Regulatory Requirements
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Clinical Research |
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14-15 |
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Clinical Trials in the MENA Region
New for 2026
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Clinical Research |
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6 |
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11 |
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Conflict Management for Pharmaceutical Executives
New for 2026
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Leadership & Management for Life Sciences |
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13-16 |
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Cosmetovigilance
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Cosmetics |
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18-19 |
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8-9 |
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Crisis Management from a Tactical Operations Perspective: A Practical Guide for Managers in the Pharmaceutical Sector
New for 2026
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Leadership & Management for Life Sciences |
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23 |
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Cyber Security for Medical Devices
|
Medical Devices |
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8-9 |
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Data Integrity Auditor Masterclass
|
GxP |
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22-23 |
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14-15 |
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Data Integrity and Document Management
|
Medical Devices |
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22 |
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8 |
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Dealing With Scientific Journal Reviewers: From Comments to Resubmission
New for 2026
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Medical Devices |
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15 |
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1 |
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Development of Combination Products: Critical Interactions
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GxP |
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16-17 |
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Difficult Conversations and Influence in Regulated Environments
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Leadership & Management for Life Sciences |
|
27 |
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19 |
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Digital CMC
New for 2026
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Medical Technology |
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6 |
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2 |
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Digital CMC: The Key To Realising Pharma 4.0
New for 2026
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Regulatory Affairs |
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23 |
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4 |
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Digital Technology Transfers
New for 2026
|
Medical Technology |
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22 |
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Drafting Commercial Contracts for the Pharmaceutical Industry
|
Commercial Contracts |
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20-21 |
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11-12 |
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EU Pharmaceutical Regulations and Strategy
|
Regulatory Affairs |
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5-6 |
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EU Proposed Pharmaceutical Legislation Changes
|
Regulatory Affairs |
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1 |
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Effective Change Management in Pharma
New for 2026
|
GxP |
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17 |
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9 |
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Effective Communication & Negotiation in Technology Transfers
New for 2026
|
GxP |
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18 |
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15 |
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Effective Deviation Management Systems in Pharma
New for 2026
|
GxP |
20 |
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25 |
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Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains
New for 2026
|
GxP |
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15 |
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20 |
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Effective Technical Writing & Editing
|
Medical Writing |
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15 |
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18 |
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Effective Technology Transfer
|
GxP |
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8-9 |
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8-9 |
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Effective Training Skills in the Pharma Industry
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Leadership & Management for Life Sciences |
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16-17 |
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1-2 |
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Ensuring Clinical Research Quality & Patient Safety
New for 2026
|
GxP |
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14 |
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Essential Documentation Skills for Clinical Research Compliance
New for 2026
|
GxP |
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5 |
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FDA Approval Process for Medical Devices
|
Medical Devices |
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30-1 |
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1-2 |
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Finance for Non-Financial Leaders in the Pharmaceutical Industry
New for 2026
|
Leadership & Management for Life Sciences |
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14-15 |
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19-20 |
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GCP and Clinical Research Update: What Inspectors Are Focusing on Now
|
Clinical Research |
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19 |
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20 |
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GMP Principles in Vaccine Manufacturing
|
GxP |
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16-17 |
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8-9 |
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Global Market Access for Medical Device Software
New for 2026
|
Medical Devices |
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8-9 |
|
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30-1 |
|
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|
Golden Rules of Being a Successful GMP Auditor
New for 2026
|
GxP |
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30-1 |
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Good Distribution Practices of Pharmaceuticals and APIs
|
GxP |
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14-15 |
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16-17 |
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Good Writing Practice for Clinical Research: Ethics, Standards & Compliance
New for 2026
|
GxP |
|
20 |
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18 |
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|
How to Audit Pharmaceutical Suppliers (Material and Service)
New for 2026
|
GxP |
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14-15 |
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How to Deal with Difficult Situations in GMP Audits
New for 2026
|
GxP |
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28 |
|
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How to Interview During GMP Audits
|
GxP |
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24 |
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How to Manage Internal GMP Audits
New for 2026
|
GxP |
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21-22 |
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How to Pass International Health Authority Inspections
New for 2026
|
GxP |
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16-17 |
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7-8 |
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How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits
New for 2026
|
GxP |
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18-19 |
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10-11 |
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ICH GCP E6 (R3): What You Need to Know for Implementation and Inspection
New for 2026
|
Clinical Research |
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13 |
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ICH Q9(R1) Quality Risk Management (QRM)
|
GxP |
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25 |
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4 |
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Interpersonal Project Management Skills for the Life Sciences Industries
New for 2026
|
Leadership & Management for Life Sciences |
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16-17 |
|
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Introduction to Veterinary Pharmacovigilance
|
Animal Health |
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16-17 |
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Introduction to the In-Vitro Diagnostic Regulation (IVDR)
|
Medical Devices |
|
16-17 |
|
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15-16 |
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Literature Searching in Drug Safety
|
Vigilance |
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14-15 |
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10-11 |
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MBA Strategic Thinking for Pharma and Biopharma Professionals
|
Leadership & Management for Life Sciences |
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21-22 |
|
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Managing Human Error: A Strategic Approach for Pharmaceutical Managers
New for 2026
|
Leadership & Management for Life Sciences |
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1 |
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Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
|
Animal Health |
|
13-14 |
|
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15-16 |
|
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|
Masterclass: Market Authorisation of AI-enabled Medical Devices
|
Artificial Intelligence (AI) in Life Sciences |
|
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29-30 |
|
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8-9 |
|
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Mastering CTD Submissions in the MENA Region
|
Regulatory Affairs |
|
|
19 |
|
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|
26 |
|
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Mastering Computer System Validation
|
GxP |
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|
17-18 |
|
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|
10-11 |
|
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|
Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP)
New for 2026
|
Medical Writing |
|
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8 |
|
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Mastering Grant Writing: Essential Skills for Crafting Winning Proposals
New for 2026
|
Medical Writing |
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22-23 |
|
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8-9 |
|
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|
Mastering Health & Safety Leadership in the Pharmaceutical Industry
New for 2026
|
Leadership & Management for Life Sciences |
|
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10 |
|
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18 |
|
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|
Measuring Performance in Clinical Research Management
|
Clinical Research |
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6 |
|
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23 |
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Medical Device Regulation in the Eurasian Union, Russia and the CIS
|
Medical Devices |
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30-1 |
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8-9 |
|
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Medical Device Regulations in Asia-Pacific Markets
|
Medical Devices |
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16-17 |
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Medical Device Regulations in the Middle East and North Africa
|
Medical Devices |
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18-19 |
|
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18-19 |
|
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|
Medical Device Single Audit Programme (MDSAP)
|
Medical Devices |
|
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25-26 |
|
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25-26 |
|
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Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
|
Medical Devices |
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22-26 |
|
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|
Medical Editing for Peer-Reviewed Journals
New for 2026
|
Medical Writing |
|
|
8 |
|
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4 |
|
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|
Medical Writing Excellence: Crafting Compelling Scientific Documents
New for 2026
|
Medical Writing |
|
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|
30-1 |
|
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|
Medical Writing for Consumers
New for 2026
|
Medical Writing |
|
21 |
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1 |
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Medical Writing for Medical Devices
|
Medical Devices |
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25-26 |
|
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30-1 |
|
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|
Medical Writing with AI
New for 2026
|
Artificial Intelligence (AI) in Life Sciences |
|
|
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18 |
|
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8 |
|
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|
Mergers & Acquisitions and Partnerships in the Pharmaceutical Sector
New for 2026
|
Leadership & Management for Life Sciences |
|
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24-26 |
|
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25-27 |
|
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|
Metered Dose Inhaler (MDI) Technology
|
Medical Devices |
|
27-28 |
|
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7-8 |
|
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|
Microbiomics in Clinical Trials
New for 2026
|
Clinical Research |
|
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|
14 |
|
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Modern Agile Leadership for Pharma and Biopharma Professionals: Adapting to a Changing Workplace
|
Leadership & Management for Life Sciences |
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11-12 |
|
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16-17 |
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|
Molecular Biology for the Non-Molecular Biologist
|
Biopharma |
|
20-21 |
|
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8-9 |
|
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|
Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass
Updated for 2026
|
Regulatory Affairs |
|
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|
12 |
|
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4 |
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|
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products
Updated for 2026
|
Medical Devices |
|
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|
14-15 |
|
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|
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests
New for 2026
|
Medical Devices |
|
|
15 |
|
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|
9 |
|
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|
Negotiation Skills for Pharma Professionals: Cross-Border, Virtual and AI Enabled Dealmaking
New for 2026
|
Leadership & Management for Life Sciences |
|
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|
15-16 |
|
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|
|
23-24 |
|
|
|
|
New EU GMP Annex 1: Compliant Sterile Medicinal Products
|
GxP |
|
|
19-21 |
|
|
|
|
|
24-26 |
|
|
|
|
Non-Conformance and Corrective Action for Medical Device Manufacturers
|
Medical Devices |
|
|
|
19 |
|
|
|
|
|
10 |
|
|
|
Orphan Drug Regulatory Masterclass: EU & US Insights
|
Regulatory Affairs |
|
|
|
|
|
|
|
6 |
|
|
|
|
|
Pharmaceutical Development of ATMPs
|
GxP |
18-19 |
|
|
|
|
|
28-29 |
|
|
|
|
|
|
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success
|
GxP |
|
|
|
|
|
|
22-24 |
|
|
|
|
|
|
Pharmaceutical Regulatory Affairs in Africa
|
Regulatory Affairs |
|
|
6-7 |
|
|
|
|
|
3-4 |
|
|
|
|
Pharmaceutical Regulatory Affairs in Asia
|
Regulatory Affairs |
24-26 |
|
|
|
|
|
|
20-22 |
|
|
|
|
|
Pharmaceutical Regulatory Affairs in China
|
Regulatory Affairs |
|
|
|
3-4 |
|
|
|
|
25-26 |
|
|
|
|
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS
|
Regulatory Affairs |
5-6 |
|
|
|
|
|
30-1 |
|
|
|
|
|
|
Pharmaceutical Regulatory Affairs in the Middle East
|
Regulatory Affairs |
|
|
|
|
|
|
|
20-21 |
|
|
|
|
|
Pharmaceutical Regulatory Affairs in the Middle East and North Africa
New for 2026
|
Regulatory Affairs |
|
|
|
2-4 |
|
|
|
|
|
|
|
|
|
Pharmacovigilance Aspects of Licensing Agreements
|
Vigilance |
|
|
|
25 |
|
|
|
|
|
10-11 |
|
|
|
Pharmacovigilance QMS & Inspection Preparation
|
Vigilance |
|
27-28 |
|
|
|
|
|
8-9 |
|
|
|
|
|
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection
|
Vigilance |
|
30 |
|
|
|
|
|
5-6 |
|
|
|
|
|
Positive Persuading and Influencing Skills for Pharma Professionals
|
Leadership & Management for Life Sciences |
|
|
18-21 |
|
|
|
|
|
2-5 |
|
|
|
|
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)
New for 2026
|
Medical Devices |
|
|
|
10-11 |
|
|
|
|
|
2-3 |
|
|
|
Practical Implementation of GCP in Veterinary Field Studies
|
Animal Health |
|
|
13-14 |
|
|
|
|
|
24-25 |
|
|
|
|
Practical Requirements of the Arab Pharmacovigilance Guidelines
|
Vigilance |
|
21-22 |
|
|
|
|
|
21-22 |
|
|
|
|
|
Practical Risk Management in Clinical Research and Trials
|
Clinical Research |
|
24 |
|
|
|
|
|
6 |
|
|
|
|
|
Process Validation for Medical Devices
|
Medical Devices |
|
|
|
4-5 |
|
|
|
|
|
3-4 |
|
|
|
Process Validation with Qualification
|
GxP |
|
|
|
3-4 |
|
|
|
|
|
1-2 |
|
|
|
Project Management for Pharma Professionals
|
Leadership & Management for Life Sciences |
9-10 |
|
|
|
2-3 |
|
|
|
30-1 |
|
|
|
|
Project Management for Regulatory Affairs Professionals
New for 2026
|
Leadership & Management for Life Sciences |
|
20-21 |
|
|
|
|
|
8-9 |
|
|
|
|
|
Protein Engineering for Pharmaceutical Biotechnology
New for 2026
|
Biopharma |
|
|
|
|
7-8 |
|
|
|
|
|
|
|
|
Registration of Veterinary Pharmaceuticals in China
New for 2026
|
Animal Health |
|
16 |
|
|
|
|
|
22 |
|
|
|
|
|
Regulatory Compliance and Safety Standards for Aesthetic Devices
New for 2026
|
Cosmetics |
|
|
|
12 |
|
|
|
|
|
4 |
|
|
|
Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP)
New for 2026
|
Vigilance |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
Root Cause Analysis and Critical Thinking
|
Leadership & Management for Life Sciences |
|
|
18 |
|
|
|
|
|
23 |
|
|
|
|
Selecting the Best Scientific Journal for Your Research
New for 2026
|
Medical Devices |
|
13 |
|
|
|
|
|
19 |
|
|
|
|
|
Signal Detection and Regulatory Expectations
|
Vigilance |
|
|
|
|
|
|
30-1 |
|
|
|
|
|
|
Signal Detection: A Comprehensive Introduction
New for 2026
|
Vigilance |
|
|
|
|
1 |
|
|
|
|
|
|
|
|
Smart Packaging and Electronic Patient Information
|
Medical Devices |
|
|
21 |
|
|
|
|
|
2-3 |
|
|
|
|
Stability Testing of Pharmaceuticals and Biopharmaceuticals
|
GxP |
|
|
20-22 |
|
|
|
|
|
9-11 |
|
|
|
|
Sterilization of Medical Devices
|
Medical Devices |
|
23-24 |
|
|
|
|
|
12-13 |
|
|
|
|
|
Successful Medical Writing – from Protocol to CTD
|
Medical Writing |
|
|
|
|
|
|
22-23 |
|
|
|
|
|
|
Sustainable Product Design for MedTech Engineers and Developers
|
Medical Devices |
|
|
7-8 |
|
|
|
|
|
26-27 |
|
|
|
|
The 2024 EU AI Act
New for 2026
|
Artificial Intelligence (AI) in Life Sciences |
|
|
|
23 |
|
|
|
|
|
3 |
|
|
|
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA
|
Animal Health |
|
|
|
15-18 |
|
|
|
|
|
|
|
|
|
The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries
New for 2026
|
Biopharma |
|
|
|
|
|
|
15-16 |
|
|
|
|
|
|
The Common Technical Document
|
GxP |
|
|
14-15 |
|
|
|
|
21-22 |
|
|
|
|
|
The FDA Drug Approval Process
|
Regulatory Affairs |
|
|
|
|
|
|
24-25 |
|
|
|
|
|
|
The Future of Bioplastics in the Medical Industry
New for 2026
|
Medical Technology |
|
|
|
|
|
|
29 |
|
|
|
|
|
|
The Future of Manufacturing: 3D Printing for Medical Devices
New for 2026
|
Medical Devices |
|
|
|
17 |
|
|
|
|
|
9 |
|
|
|
The Pharma Mini MBA
|
Leadership & Management for Life Sciences |
18-20 |
|
|
|
8-10 |
|
|
|
4-6 |
|
|
|
|
The Principles & Applications of CRISPR
New for 2026
|
Biopharma |
|
|
|
|
7 |
|
|
|
|
|
|
|
|
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
|
Regulatory Affairs |
|
20-21 |
|
|
|
|
|
12-13 |
|
|
|
|
|
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR
|
Medical Devices |
|
|
|
|
|
|
21 |
|
|
|
|
|
|
Thinking Outside of the GMP Box
|
GxP |
|
|
|
|
|
|
16-17 |
|
|
|
|
|
|
UK Conformity Assessed (UKCA) Marking for Medical Devices
|
Medical Devices |
|
15 |
|
|
|
|
|
21 |
|
|
|
|
|
US FDA - Understanding Key Factors When Working with the FDA
|
Biopharma |
|
|
12 |
|
|
|
|
|
25 |
|
|
|
|
Understanding Scientific Journal Submission and Publication
New for 2026
|
Medical Devices |
|
|
11 |
|
|
|
|
|
16 |
|
|
|
|
Understanding Toxicology: A Guide for Non-Toxicologists
New for 2026
|
Regulatory Affairs |
|
|
|
|
15 |
|
|
|
|
|
|
|
|
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers
|
Medical Devices |
|
|
|
8 |
|
|
|
|
30 |
|
|
|
|
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry
New for 2026
|
GxP |
|
|
|
11 |
|
|
|
|
18 |
|
|
|
|
Variations to Marketing Authorisations
|
Regulatory Affairs |
|
|
|
2-3 |
|
|
|
|
11-12 |
|
|
|
|
Veterinary Pharmaceutical Submissions in the EU
|
Animal Health |
|
|
18-19 |
|
|
|
|
|
19-20 |
|
|
|
|
Writing Inspection-Ready SOPs: Best Practice for Compliance and Control
|
Regulatory Affairs |
26 |
|
|
|
14 |
|
|
|
26 |
|
|
|