Pharmaceutical Training Course Calendar

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Our Pharmaceutical calendar for the next 12 months:

Live online Classroom 2025 2026
Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep
A Practical Guide to Producing and Maintaining the PSMF Vigilance 13 29
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 12 20
A Practical Introduction to Good Clinical Practice (GCP) GxP 15
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Artificial Intelligence (AI) in Life Sciences 6 6
AI in Pharmacovigilance Artificial Intelligence (AI) in Life Sciences 19
Achieving Publication Success in Scientific Journals Medical Writing 2 21
Additional Risk Minimization Measures (aRMMs) and Their Effectiveness Vigilance 3
Advanced Pharmacovigilance: From Performing Successful Due Diligence to Benefit-Risk Assessments – What to Consider Vigilance 23-25 21-25
An Essential Overview of Medical Information Regulatory Affairs 4 22
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 12 28
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 20 8
An Introduction to Signal Detection Vigilance 16
An Introduction to Technology Transfer for Solid Dosage Forms GxP 14 6 18
An Overview of EU and UK Regulatory Affairs Regulatory Affairs 11-12 21-22
An Overview of Ethical Standards in Clinical Research Publication GxP 13
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions Regulatory Affairs 10 10
Balancing Costs and Compliance: The Financial Side of GMP GxP 6
Best Practice for Writing Effective SOPs Regulatory Affairs 4 26 14
Best Practices for Supplier Qualification in Life Science GxP 13-14 6-7
Biosimilars Biopharma 16-17 22-23
Biotechnology for the Non-Biotechnologist Biopharma 10-14
Building The Business Case For Pharma 4.0 Medical Technology 13
CAPA (Corrective and Preventative Action) Regulatory Affairs 5 15
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 20-21 23-24
Cleaning Validation - Best Practice in Pharmaceuticals GxP 2-3 23-24
Clinical & Post-Marketing Safety Vigilance 11-12
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 16-17 30-1
Clinical Quality Management Systems Clinical Research 23-24 17-18
Clinical Trial Agreements: Key Legal, Regulatory and IP Considerations for the EU and UK Markets Commercial Contracts 28 18 2
Clinical Trial Monitoring Clinical Research 29-30
Clinical Trial Regulatory Requirements Clinical Research 2-3 14-15
Competition Law for the Pharmaceutical Industry Commercial Contracts 27
Conflict Management for Pharmaceutical Executives Conflict Management 26-29 13-16
Cosmetovigilance Vigilance 18-19
Data Integrity Auditor Masterclass GxP 15-16 22-23
Data Integrity and Document Management GxP 11 22
Dealing With Scientific Journal Reviewers: From Comments to Resubmission Medical Writing 24 15
Demystifying European Post-Marketing Pharmacovigilance Vigilance 3-7
Development of Combination Products: Critical Interactions GxP 9-10 16-17
Digital CMC Medical Technology 6
Digital CMC: The Key To Realising Pharma 4.0 GxP 1 23
Digital Technology Transfers Medical Technology 4 22
Digital Technology and Personalisation in Patient Support Programmes Clinical Research 6
Drafting Commercial Contracts for the Pharmaceutical Industry Commercial Contracts 12-13 20-21
EU Pharmaceutical Regulations and Strategy Regulatory Affairs 2-3
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 19 1
Effective Change Management in Pharma GxP 17
Effective Communication & Negotiation in Technology Transfers GxP 18
Effective Deviation Management Systems in Pharma GxP 20 25
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 21 15
Effective Technical Writing & Editing Medical Writing 15
Ensuring Clinical Research Quality & Patient Safety GxP 2 14
Essential Documentation Skills for Clinical Research Compliance GxP 9
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 21 19
GMP Principles in Vaccine Manufacturing GxP 10-11 16-17
Golden Rules of Being a Successful GMP Auditor GxP 5-6 30-1
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18 14-15
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance GxP 20
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 26-27 14-15
How to Deal with Difficult Situations in GMP Audits GxP 5 28
How to Interview During GMP Audits GxP 10 12 24
How to Manage Internal GMP Audits GxP 24-25 21-22
How to Pass International Health Authority Inspections GxP 16-17
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits GxP 3-4 18-19
Interpersonal Project Management Skills for the Life Sciences Industries Project Management 22-23 16-17
Literature Searching in Drug Safety Vigilance 14-15
MBA Strategic Thinking for Pharma and Biopharma Professionals Leadership & Strategy 30-31 23-24 21-22
Managing Human Error: A Strategic Approach for Pharmaceutical Managers Health & Safety 28 1
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 13-14
Mastering CTD Submissions in the MENA Region Regulatory Affairs 28 19
Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP) Medical Writing 20 8
Mastering Grant Writing: Essential Skills for Crafting Winning Proposals Medical Writing 22-23
Medical Editing for Peer-Reviewed Journals Medical Writing 8
Medical Writing Excellence: Crafting Compelling Scientific Documents Medical Writing 4-5 30-1
Medical Writing for Consumers Medical Writing 21
Medical Writing with AI Artificial Intelligence (AI) in Life Sciences 18
Metrics and Earned Value in Clinical Research Projects Clinical Research 24 6
Microbiomics in Clinical Trials Clinical Research 26 14
Modern Agile Leadership for Pharma and Biopharma Professionals: Adapting to a Changing Workplace Leadership & Strategy 17-18 11-12
Molecular Biology for the Non-Molecular Biologist Biopharma 20-21
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 2-3 14-15
Navigating ICH GCP E6 (R3): What You Need to Know Clinical Research 29 13
New EU GMP Annex 1: Compliant Aseptic Operations GxP 25-27 19-21
Orphan Drug Regulatory Masterclass: EU & US Insights Regulatory Affairs 4
Pharmaceutical Development of ATMPs GxP 18-19 28-29
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success GxP 26-28 6-8
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 4-5 6-7
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 24-26
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 26-27 12-13
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 5-6 30-1
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 24-25
Pharmacovigilance Aspects of Licensing Agreements Vigilance 1-2 25
Pharmacovigilance QMS & Inspection Preparation Vigilance 27-28
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection Vigilance 30
Positive Persuading and Influencing Skills for Pharma Professionals Management 10-13 18-21
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 21-22
Project Management for Pharma Professionals Project Management 10-11 9-10 2-3
Protein Engineering for Pharmaceutical Biotechnology Biopharma 21-22 7-8
Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma Artificial Intelligence (AI) in Life Sciences 19 22
Root Cause Analysis and Critical Thinking Management 24 18
Selecting the Best Scientific Journal for Your Research Medical Writing 10 13
Signal Detection and Regulatory Expectations Vigilance 18-21 2-3 30-1
Signal Detection: A Comprehensive Introduction Vigilance 28 1
Smart Packaging and Electronic Patient Information GxP 3-4 15
Software Automation in Research and Development (R&D) Clinical Trials Clinical Research 17 28
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 10-11 20-21
Successful Cognitive Testing in Clinical Drug Trials: Biomarkers, Test Selection & Integration Clinical Research 16 18
Successful Medical Writing – from Protocol to CTD Medical Writing 23-24 22-23
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 23
The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries Biopharma 12-13 11-12 15-16
The Common Technical Document GxP 24-25 27-28 14-15
The FDA Drug Approval Process Regulatory Affairs 23-24 24-25
The Financial Benefits of Change Management GxP 13
The Financial Benefits of Pharmaceutical Quality Systems GxP 13 30
The Financial Benefits of Quality Risk Management GxP 17
The Financial Benefits of Validation Master Plans GxP 6
The Pharma Mini MBA Leadership & Strategy 5-7 18-20 8-10
The Principles & Applications of CRISPR Biopharma 23 7
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 20-21
Thinking Outside of the GMP Box GxP 3-4 16-17
US FDA - Understanding Key Factors When Working with the FDA Biopharma 26 12
Understanding Active Pharmaceutical Ingredients (APIs) GxP 19-20 29-30
Understanding Computer System Validation (CSV) GxP 24-25 17-18
Understanding Scientific Journal Submission and Publication Medical Writing 17 11
Understanding Toxicology: A Guide for Non-Toxicologists Regulatory Affairs 19 15
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 5 11
Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes Clinical Research 16
Variations to Marketing Authorisations Regulatory Affairs 29-30 2-3
Working with Emotional Intelligence in the Pharmaceutical and Biopharma Industry Leadership & Strategy 27