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Live online
Classroom
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2027 |
2028 |
| 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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6 |
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2 |
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A Practical Approach to Veterinary Vaccine Development and Registration in the EU
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Animal Health |
9-10 |
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22-23 |
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A Practical Guide to Producing and Maintaining the PSMF & Annexes
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Vigilance |
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15 |
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A Practical Guide to Writing Risk Management Plans (RMPs)
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Vigilance |
19 |
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18 |
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A Practical Introduction to Good Clinical Practice (GCP)
New for 2027
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GxP |
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14 |
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5 |
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A Practical Overview of Pre-Filled Syringes
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Medical Devices |
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24-25 |
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10-11 |
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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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10 |
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12 |
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AI in Healthcare: Governance, Risk & Strategic Adoption
New for 2027
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Artificial Intelligence (AI) in Life Sciences |
9 |
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21 |
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AI in Pharmacovigilance
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Artificial Intelligence (AI) in Life Sciences |
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17 |
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17 |
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APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence
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GxP |
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28-29 |
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20-21 |
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Additional Risk Minimization Measures (aRMMs) and Their Effectiveness
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Vigilance |
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15 |
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14 |
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Advanced GMP & GDP Auditor Masterclass
New for 2027
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GxP |
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12-14 |
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12-14 |
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Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider
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Vigilance |
1-3 |
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20-24 |
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Advanced Veterinary Pharmacovigilance
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Animal Health |
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10-11 |
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3-4 |
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An Essential Overview of Medical Information
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Regulatory Affairs |
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21 |
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2 |
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An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices
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Medical Devices |
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13 |
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8 |
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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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7 |
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18 |
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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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An Introduction to the Design and Development of Medical Devices and Device-Drug Combination (DDC) Products
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Medical Devices |
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28-29 |
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8-9 |
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An Overview of EU and UK Regulatory Affairs
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Regulatory Affairs |
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20-21 |
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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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Animal Feed and Feed Additive Registration in China and Thailand
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Animal Health |
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15 |
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21 |
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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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9 |
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8 |
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Behavioural Risk Management in Clinical Trials
New for 2027
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Clinical Research |
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15 |
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19 |
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Best Practices for Supplier Qualification in Life Science
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Medical Devices |
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26-27 |
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11-12 |
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Biological Evaluation of Medical Devices
|
Medical Devices |
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1-2 |
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Biosimilars
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Biopharma |
15-16 |
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20-21 |
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Biotechnology for the Non-Biotechnologist
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Biopharma |
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CAPA (Corrective and Preventative Action)
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Regulatory Affairs |
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14 |
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3 |
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Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
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GxP |
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22-23 |
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18-19 |
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Cleaning Validation - Best Practice in Pharmaceuticals
|
GxP |
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22-23 |
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23-24 |
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Cleanroom Requirements for Medical Device Manufacturers
|
Medical Devices |
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20 |
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Clinical & Post-Marketing Safety
New for 2026
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Vigilance |
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10-11 |
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15-16 |
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Clinical Evaluation of Medical Device Software and Software as a Medical Device
|
Medical Devices |
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21 |
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7 |
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Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications
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Regulatory Affairs |
3-4 |
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29-30 |
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Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness
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Clinical Research |
15-16 |
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16-17 |
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Clinical Research Project Management
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Leadership & Management for Life Sciences |
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28-30 |
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20-22 |
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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 |
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12 |
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23 |
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Clinical Trial Monitoring
|
Clinical Research |
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17-18 |
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9-10 |
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Clinical Trial Regulatory Requirements
|
Clinical Research |
1-2 |
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23-24 |
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Clinical Trials in the MENA Region
New for 2026
|
Clinical Research |
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26 |
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10 |
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Competition Law for the Pharmaceutical Industry
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Commercial Contracts |
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8 |
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Conflict Management for Pharmaceutical Executives
New for 2027
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Leadership & Management for Life Sciences |
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27-28 |
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Cosmetovigilance
|
Cosmetics |
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17-18 |
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9-10 |
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Data Integrity and Document Management
|
Medical Devices |
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21 |
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13 |
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Data-Driven Process Control: Statistical Process Control (SPC) Tools for Quality, Stability, and Performance
New for 2027
|
GxP |
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27-28 |
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Dealing With Scientific Journal Reviewers: From Comments to Resubmission
New for 2026
|
Medical Devices |
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Development of Combination Products: Critical Interactions
|
GxP |
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15-16 |
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Difficult Conversations and Influence in Regulated Environments
|
Leadership & Management for Life Sciences |
|
26 |
|
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18 |
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Drafting Commercial Contracts for the Pharmaceutical Industry
|
Commercial Contracts |
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19-20 |
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10-11 |
|
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EU Pharmaceutical Regulations and Strategy
|
Regulatory Affairs |
1-2 |
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4-5 |
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EU Proposed Pharmaceutical Legislation Changes
|
Regulatory Affairs |
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7 |
|
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Effective Technical Writing & Editing
|
Medical Writing |
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14 |
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17 |
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Effective Technology Transfer
|
GxP |
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7-8 |
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7-8 |
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|
FDA Approval Process for Medical Devices
|
Medical Devices |
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24-25 |
|
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30-1 |
|
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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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13-14 |
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18-19 |
|
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|
GMP Advanced Masterclass for Pharmaceutical and Biotechnology Industries
New for 2026
|
GxP |
|
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7-9 |
|
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|
8-10 |
|
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|
GMP Principles in Vaccine Manufacturing
|
GxP |
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15-16 |
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13-14 |
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|
Good Distribution Practices of Pharmaceuticals and APIs
|
GxP |
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20-21 |
|
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15-16 |
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|
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance
New for 2026
|
GxP |
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How the Pharmaceutical and Biotech Industries Work: From Molecule to Market
|
Regulatory Affairs |
11 |
|
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|
27 |
|
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|
ICH Q12: Advanced Pharmaceutical Product Lifecycle Management in Practice
New for 2027
|
GxP |
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7-8 |
|
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ICH Q9(R1) Quality Risk Management (QRM)
|
GxP |
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24 |
|
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3 |
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|
Integrating AI into the GMP Environment
New for 2026
|
Artificial Intelligence (AI) in Life Sciences |
|
|
7 |
|
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|
5 |
|
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|
Interpersonal Project Management Skills for the Life Sciences Industries
|
Leadership & Management for Life Sciences |
|
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|
8-9 |
|
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Introduction to Veterinary Pharmacovigilance
|
Animal Health |
8-9 |
|
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15-16 |
|
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Literature Searching in Drug Safety
|
Vigilance |
|
|
13-14 |
|
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|
9-10 |
|
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MBA Frameworks for Strategic Thinking in Pharma & Biopharma
|
Leadership & Management for Life Sciences |
|
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|
20-21 |
|
|
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|
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
|
Animal Health |
|
12-13 |
|
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|
14-15 |
|
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|
Masterclass: Market Authorisation of AI-enabled Medical Devices
|
Artificial Intelligence (AI) in Life Sciences |
|
|
|
28-29 |
|
|
|
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|
7-8 |
|
|
|
Mastering CTD Submissions in the MENA Region
|
Regulatory Affairs |
|
|
25 |
|
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|
25 |
|
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|
Mastering Computer System Validation
|
GxP |
|
|
|
16-17 |
|
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|
|
9-10 |
|
|
|
Mastering Grant Writing: Essential Skills for Crafting Winning Proposals
New for 2026
|
Medical Writing |
|
|
|
|
|
|
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|
Mastering Health & Safety Leadership in the Pharmaceutical Industry
New for 2026
|
Leadership & Management for Life Sciences |
|
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|
Measuring Performance in Clinical Research Management
|
Clinical Research |
|
|
17 |
|
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|
19 |
|
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|
Medical Device Cybersecurity and Regulatory Compliance
|
Medical Devices |
18-19 |
|
|
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|
30-1 |
|
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Medical Device Regulation in the Eurasian Union, Russia and the CIS
|
Medical Devices |
|
|
|
29-30 |
|
|
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|
7-8 |
|
|
|
Medical Device Regulations in Asia-Pacific Markets
|
Medical Devices |
2-3 |
|
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15-16 |
|
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Medical Device Regulations in the Middle East and North Africa
|
Medical Devices |
|
|
17-18 |
|
|
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|
17-18 |
|
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|
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
|
Medical Devices |
|
|
|
21-25 |
|
|
|
|
|
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|
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
|
Medical Devices |
16-17 |
|
|
|
|
|
16-17 |
|
|
|
|
|
|
Medical Writing for Medical Devices
|
Medical Devices |
|
|
|
16-17 |
|
|
|
|
|
1-2 |
|
|
|
Medical Writing with AI
New for 2026
|
Artificial Intelligence (AI) in Life Sciences |
|
|
|
|
|
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|
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|
|
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|
|
Mergers & Acquisitions and Partnerships in the Pharmaceutical Sector
New for 2026
|
Leadership & Management for Life Sciences |
|
|
|
23-25 |
|
|
|
|
|
1-3 |
|
|
|
Metered Dose Inhalers (MDI) Technology in the 2020s and Beyond
|
Medical Devices |
|
26-27 |
|
|
|
|
|
6-7 |
|
|
|
|
|
Microbiomics in Clinical Trials
New for 2027
|
Clinical Research |
|
|
|
|
|
|
17 |
|
|
|
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|
Modern Agile Leadership for Pharma and Biopharma Professionals: Adapting to a Changing Workplace
|
Leadership & Management for Life Sciences |
|
|
10-11 |
|
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|
15-16 |
|
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|
Molecular Biology from Fundamentals to the Latest Applications
|
Biopharma |
|
19-20 |
|
|
|
|
|
7-8 |
|
|
|
|
|
Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass
Updated for 2026
|
Regulatory Affairs |
|
|
|
10 |
|
|
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|
3 |
|
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|
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests
New for 2026
|
Medical Devices |
|
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|
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|
Negotiation Skills for Pharma Professionals: Cross-Border, Virtual and AI Enabled Dealmaking
New for 2027
|
Leadership, Strategy & Negotiation |
|
|
24-25 |
|
|
|
|
|
22-23 |
|
|
|
|
New EU GMP Annex 1: Compliant Sterile Medicinal Products
|
GxP |
|
28-30 |
|
|
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|
|
4-6 |
|
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|
Non-Conformance and Corrective Action for Medical Device Manufacturers
|
Medical Devices |
|
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|
Orphan Drug Regulatory Masterclass: EU & US Insights
|
Regulatory Affairs |
3 |
|
|
|
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|
28 |
|
|
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|
Pharma Facility Project Management: Delivering GMP‑Compliant Sites On Time and Within Budget
New for 2027
|
GxP |
|
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|
|
15-16 |
|
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|
|
Pharmaceutical Development of ATMPs
|
GxP |
17-18 |
|
|
|
|
|
27-28 |
|
|
|
|
|
|
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success
|
GxP |
17-19 |
|
|
|
|
|
21-23 |
|
|
|
|
|
|
Pharmaceutical Regulatory Affairs in Asia
|
Regulatory Affairs |
3-5 |
|
|
|
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|
19-21 |
|
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|
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|
Pharmaceutical Regulatory Affairs in China
|
Regulatory Affairs |
|
|
19-20 |
|
|
|
|
|
24-25 |
|
|
|
|
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS
|
Regulatory Affairs |
4-5 |
|
|
|
|
|
29-30 |
|
|
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|
|
|
Pharmaceutical Regulatory Affairs in the Middle East
|
Regulatory Affairs |
|
12-13 |
|
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|
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|
19-20 |
|
|
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|
|
Pharmaceutical Regulatory Affairs in the Middle East and North Africa
New for 2026
|
Regulatory Affairs |
|
|
|
7-9 |
|
|
|
|
|
|
|
|
|
Pharmacovigilance Aspects of Licensing Agreements
|
Vigilance |
|
|
|
30 |
|
|
|
|
|
8 |
|
|
|
Pharmacovigilance QMS & Inspection Preparation
|
Vigilance |
|
26-27 |
|
|
|
|
|
7-8 |
|
|
|
|
|
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection
|
Vigilance |
|
29 |
|
|
|
|
|
4 |
|
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|
Positive Persuading and Influencing Skills for Pharma Professionals
|
Leadership & Management for Life Sciences |
|
|
26-27 |
|
|
|
|
|
1-2 |
|
|
|
|
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)
New for 2026
|
Medical Devices |
|
|
|
|
|
|
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|
Practical Implementation of GCP in Veterinary Field Studies
|
Animal Health |
|
20-21 |
|
|
|
|
|
13-14 |
|
|
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|
|
Practical Risk Management in Clinical Research and Trials
|
Clinical Research |
|
23 |
|
|
|
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|
5 |
|
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|
Preparing for GCP Inspections: Key Expectations under ICH GCP E6(R3), EU CTR and Current Regulatory Thinking
|
Clinical Research |
|
|
25 |
|
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|
19 |
|
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|
Process Validation for Medical Devices
|
Medical Devices |
|
|
|
10-11 |
|
|
|
|
|
2-3 |
|
|
|
Process Validation with Qualification
|
GxP |
|
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|
14-15 |
|
|
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|
1-2 |
|
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|
Project Management for Pharma Professionals
|
Leadership & Management for Life Sciences |
|
|
13-14 |
|
|
|
|
|
29-30 |
|
|
|
|
Project Management for Regulatory Affairs Professionals
New for 2027
|
Leadership & Management for Life Sciences |
|
19-20 |
|
|
|
|
|
7-8 |
|
|
|
|
|
Protein Engineering for Pharmaceutical Biotechnology
New for 2027
|
Biopharma |
|
|
|
|
|
|
21-22 |
|
|
|
|
|
|
Registration of Veterinary Pharmaceuticals in China
New for 2026
|
Animal Health |
|
15 |
|
|
|
|
|
21 |
|
|
|
|
|
Regulatory Compliance and Safety Standards for Aesthetic Devices
New for 2026
|
Cosmetics |
|
|
|
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|
|
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|
|
Root Cause Analysis and Critical Thinking
|
Leadership & Management for Life Sciences |
|
|
24 |
|
|
|
|
|
22 |
|
|
|
|
Selecting the Best Scientific Journal for Your Research
New for 2026
|
Medical Devices |
|
|
|
|
|
|
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|
|
Signal Detection and Regulatory Expectations
|
Vigilance |
|
|
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|
|
29-30 |
|
|
|
|
|
|
Smart Packaging and Electronic Patient Information
|
Medical Devices |
|
|
20 |
|
|
|
|
|
2 |
|
|
|
|
Stability Testing of Pharmaceuticals and Biopharmaceuticals
|
GxP |
|
|
19-21 |
|
|
|
|
|
8-10 |
|
|
|
|
Sterilization of Medical Devices
|
Medical Devices |
|
22-23 |
|
|
|
|
|
11-12 |
|
|
|
|
|
Successful Medical Writing – from Protocol to CTD
|
Medical Writing |
11-12 |
|
|
|
|
|
21-22 |
|
|
|
|
|
|
Sustainable Product Design for MedTech Engineers and Developers
|
Medical Devices |
|
|
6-7 |
|
|
|
|
|
25-26 |
|
|
|
|
The 2024 EU AI Act
New for 2026
|
Artificial Intelligence (AI) in Life Sciences |
|
|
|
22 |
|
|
|
|
|
2 |
|
|
|
The Common Technical Document
|
GxP |
|
13-14 |
|
|
|
|
|
20-21 |
|
|
|
|
|
The FDA Drug Approval Process
|
Regulatory Affairs |
|
|
|
|
|
|
23-24 |
|
|
|
|
|
|
The Future of Bioplastics in the Medical Industry
New for 2027
|
Medical Devices |
10 |
|
|
|
|
|
28 |
|
|
|
|
|
|
The Future of Manufacturing: 3D Printing for Medical Devices
New for 2026
|
Medical Devices |
|
|
|
16 |
|
|
|
|
|
8 |
|
|
|
The Pharma Mini MBA
|
Leadership & Management for Life Sciences |
|
|
19-21 |
|
|
|
|
|
10-12 |
|
|
|
|
The Principles & Applications of CRISPR
New for 2027
|
Biopharma |
|
|
|
|
6 |
|
|
|
|
|
|
|
|
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
|
Regulatory Affairs |
|
19-20 |
|
|
|
|
|
11-12 |
|
|
|
|
|
Thinking Beyond Traditional GMP
|
GxP |
9-10 |
|
|
|
|
|
15-16 |
|
|
|
|
|
|
UK Conformity Assessed (UKCA) Marking for Medical Devices
|
Medical Devices |
|
14 |
|
|
|
|
|
20 |
|
|
|
|
|
US FDA - Understanding Key Factors When Working with the FDA
|
Biopharma |
|
|
|
|
7 |
|
|
|
|
|
|
|
|
Understanding Pharmacovigilance Regulations in China
New for 2027
|
Vigilance |
|
27 |
|
|
|
|
|
11 |
|
|
|
|
|
Understanding Scientific Journal Submission and Publication
New for 2026
|
Medical Devices |
|
|
|
|
|
|
|
|
|
|
|
|
|
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers
|
Medical Devices |
|
|
|
7 |
|
|
|
|
29 |
|
|
|
|
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry
New for 2026
|
GxP |
|
|
|
|
|
|
|
|
|
|
|
|
|
Variations to Marketing Authorisations
|
Regulatory Affairs |
|
|
|
14-15 |
|
|
|
|
10-11 |
|
|
|
|
Veterinary Pharmaceutical Submissions in the EU
|
Animal Health |
|
|
17-18 |
|
|
|
|
|
18-19 |
|
|
|
|
Writing Inspection-Ready SOPs: Best Practice for Compliance and Control
|
Regulatory Affairs |
|
|
6 |
|
|
|
|
|
25 |
|
|
|