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2026 |
2027 |
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Aug |
Sep |
Oct |
Nov |
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Feb |
Mar |
Apr |
May |
Jun |
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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 |
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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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6 |
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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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AI in Pharmacovigilance
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Artificial Intelligence (AI) in Life Sciences |
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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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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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2 |
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Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider
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Vigilance |
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21-25 |
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An Essential Overview of Medical Information
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Regulatory Affairs |
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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 Human Factors for Pharmaceutical and Medical Device Professionals
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Medical Devices |
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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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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 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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11 |
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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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Behavioural Risk Management in Clinical Trials
New for 2026
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Clinical Research |
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5 |
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Best Practice for Writing Effective SOPs
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Regulatory Affairs |
14 |
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26 |
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Best Practices for Supplier Qualification in Life Science
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Medical Devices |
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12-13 |
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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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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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6 |
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CAPA (Corrective and Preventative Action)
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Regulatory Affairs |
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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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19-20 |
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Cleaning Validation - Best Practice in Pharmaceuticals
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GxP |
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1-2 |
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Clinical & Post-Marketing Safety
New for 2026
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Vigilance |
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16-17 |
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Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
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Regulatory Affairs |
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30-1 |
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Clinical Quality Management Systems
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Clinical Research |
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17-18 |
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Clinical Research Project Management
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Medical Devices |
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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 |
2 |
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24 |
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Clinical Trial Monitoring
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Clinical Research |
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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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11 |
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Competition Law for the Pharmaceutical Industry
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Commercial Contracts |
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Cosmetovigilance
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Cosmetics |
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8-9 |
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Data Integrity Auditor Masterclass
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GxP |
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14-15 |
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Data Integrity and Document Management
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Medical Devices |
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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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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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Digital CMC
New for 2026
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Medical Technology |
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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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4 |
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Digital Technology Transfers
New for 2026
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Medical Technology |
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22 |
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Digital Technology and Personalisation in Patient Support Programmes
New for 2026
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Clinical Research |
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4 |
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Drafting Commercial Contracts for the Pharmaceutical Industry
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Commercial Contracts |
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11-12 |
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EU Pharmaceutical Regulations and Strategy
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Regulatory Affairs |
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5-6 |
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EU Proposed Pharmaceutical Legislation Changes
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Regulatory Affairs |
1 |
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Effective Change Management in Pharma
New for 2026
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GxP |
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9 |
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Effective Communication & Negotiation in Technology Transfers
New for 2026
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GxP |
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15 |
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Effective Deviation Management Systems in Pharma
New for 2026
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GxP |
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25 |
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Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains
New for 2026
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GxP |
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20 |
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Effective Technical Writing & Editing
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Medical Writing |
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18 |
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Ensuring Clinical Research Quality & Patient Safety
New for 2026
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GxP |
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14 |
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Essential Documentation Skills for Clinical Research Compliance
New for 2026
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GxP |
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5 |
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GCP and Clinical Research Update: What Inspectors Are Focusing on Now
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Clinical Research |
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20 |
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GMP Principles in Vaccine Manufacturing
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GxP |
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8-9 |
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Golden Rules of Being a Successful GMP Auditor
New for 2026
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GxP |
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30-1 |
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Good Distribution Practices of Pharmaceuticals and APIs
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GxP |
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16-17 |
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Good Writing Practice for Clinical Research: Ethics, Standards & Compliance
New for 2026
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GxP |
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18 |
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How to Audit Pharmaceutical Suppliers (Material and Service)
New for 2026
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GxP |
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14-15 |
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How to Deal with Difficult Situations in GMP Audits
New for 2026
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GxP |
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28 |
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How to Interview During GMP Audits
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GxP |
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24 |
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How to Manage Internal GMP Audits
New for 2026
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GxP |
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21-22 |
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How to Pass International Health Authority Inspections
New for 2026
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GxP |
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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
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GxP |
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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
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Clinical Research |
13 |
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Literature Searching in Drug Safety
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Vigilance |
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10-11 |
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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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Mastering CTD Submissions in the MENA Region
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Regulatory Affairs |
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26 |
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Mastering Computer System Validation
|
GxP |
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10-11 |
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Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP)
New for 2026
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Medical Writing |
8 |
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Mastering Grant Writing: Essential Skills for Crafting Winning Proposals
New for 2026
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Medical Writing |
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8-9 |
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Measuring Performance in Clinical Research Management
|
Clinical Research |
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23 |
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Medical Editing for Peer-Reviewed Journals
New for 2026
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Medical Writing |
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4 |
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Medical Writing Excellence: Crafting Compelling Scientific Documents
New for 2026
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Medical Writing |
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30-1 |
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Medical Writing for Consumers
New for 2026
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Medical Writing |
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1 |
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Medical Writing with AI
New for 2026
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Artificial Intelligence (AI) in Life Sciences |
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8 |
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Microbiomics in Clinical Trials
New for 2026
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Clinical Research |
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14 |
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Molecular Biology for the Non-Molecular Biologist
|
Biopharma |
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8-9 |
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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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New EU GMP Annex 1: Compliant Sterile Medicinal Products
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GxP |
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24-26 |
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Orphan Drug Regulatory Masterclass: EU & US Insights
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Regulatory Affairs |
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6 |
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Pharmaceutical Development of ATMPs
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GxP |
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28-29 |
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Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success
|
GxP |
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22-24 |
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Pharmaceutical Regulatory Affairs in Africa
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Regulatory Affairs |
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3-4 |
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Pharmaceutical Regulatory Affairs in Asia
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Regulatory Affairs |
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20-22 |
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Pharmaceutical Regulatory Affairs in China
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Regulatory Affairs |
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25-26 |
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Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS
|
Regulatory Affairs |
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30-1 |
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Pharmaceutical Regulatory Affairs in the Middle East
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Regulatory Affairs |
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20-21 |
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Pharmaceutical Regulatory Affairs in the Middle East and North Africa
New for 2026
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Regulatory Affairs |
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Pharmacovigilance Aspects of Licensing Agreements
|
Vigilance |
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10-11 |
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Pharmacovigilance QMS & Inspection Preparation
|
Vigilance |
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8-9 |
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Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection
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Vigilance |
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5-6 |
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Practical Requirements of the Arab Pharmacovigilance Guidelines
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Vigilance |
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21-22 |
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Protein Engineering for Pharmaceutical Biotechnology
New for 2026
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Biopharma |
7-8 |
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Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma
New for 2026
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Artificial Intelligence (AI) in Life Sciences |
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2 |
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Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP)
New for 2026
|
Vigilance |
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14 |
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Risk Management in Clinical Research and Trials
|
Clinical Research |
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6 |
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Selecting the Best Scientific Journal for Your Research
New for 2026
|
Medical Devices |
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19 |
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Signal Detection and Regulatory Expectations
|
Vigilance |
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30-1 |
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Signal Detection: A Comprehensive Introduction
New for 2026
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Vigilance |
1 |
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Smart Packaging and Electronic Patient Information
|
Medical Devices |
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2-3 |
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Software Automation in Research and Development (R&D) Clinical Trials
New for 2026
|
Clinical Research |
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28 |
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Stability Testing of Pharmaceuticals and Biopharmaceuticals
|
GxP |
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9-11 |
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Successful Cognitive Testing in Clinical Drug Trials: Biomarkers, Test Selection & Integration
New for 2026
|
Clinical Research |
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18 |
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Successful Medical Writing – from Protocol to CTD
|
Medical Writing |
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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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The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries
New for 2026
|
Biopharma |
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15-16 |
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The Common Technical Document
|
GxP |
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21-22 |
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The FDA Drug Approval Process
|
Regulatory Affairs |
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24-25 |
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The Principles & Applications of CRISPR
New for 2026
|
Biopharma |
7 |
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The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
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Regulatory Affairs |
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12-13 |
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Thinking Outside of the GMP Box
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GxP |
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16-17 |
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US FDA - Understanding Key Factors When Working with the FDA
|
Biopharma |
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25 |
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Understanding Scientific Journal Submission and Publication
New for 2026
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Medical Devices |
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16 |
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Understanding Toxicology: A Guide for Non-Toxicologists
New for 2026
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Regulatory Affairs |
15 |
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Upstream and Downstream Manufacturing in the Biopharmaceutical Industry
New for 2026
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GxP |
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18 |
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Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes
New for 2026
|
Clinical Research |
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13 |
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Variations to Marketing Authorisations
|
Regulatory Affairs |
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11-12 |
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