Pharmaceutical Training Course Calendar

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Our Pharmaceutical calendar for the next 12 months:

Live online Classroom 2025 2026
Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb
A Practical Guide to Producing and Maintaining the PSMF Vigilance 23 3
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 11 12
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Clinical Research 30 6
AI in Pharmacovigilance Vigilance 7 19
Additional Risk Minimization Measures (aRMMs) and Their Effectiveness Vigilance 9 10 3
Advanced Pharmacovigilance Vigilance 24-26 2-4 6-10
Advanced Project Management in Clinical Research Clinical Research 9 3
An Essential Overview of Medical Information Regulatory Affairs 18 4
An Essential Overview of Pharmacovigilance Vigilance 15 8-9
An Essential Overview of the Medical Device Industry Regulatory Affairs 3 7
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 12 22
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 9 20
An Introduction to Pharmaceutical Packaging GxP 2-4 30-2
An Introduction to Technology Transfer for Solid Dosage Forms GxP 4 14
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions Regulatory Affairs 9 17 10
Be In the Know With Pharma 4.0: Building The Business Case For Pharma 4.0 Medical Technology 16
Be In the Know With Pharma 4.0: Digital CMC Medical Technology 19 23
Be In the Know With Pharma 4.0: Digital Technology Transfer Medical Technology 9
Best Practice for Writing Effective SOPs Regulatory Affairs 27 17 4
Best Practices for Supplier Qualification in Life Science GxP 27-28 16-17 13-14
Biosimilars Biopharma 21-22 30-1
Biotechnology for the Non-Biotechnologist Biopharma 9-11 10-14
Breaking the Code – Achieving Publication Success in Scientific Journals: Dealing with Reviewers' Comments and Resubmission Medical Writing 14 24
Breaking the Code – Achieving Publication Success in Scientific Journals: Journal Submission and Publication Medical Writing 7 17
Breaking the Code – Achieving Publication Success in Scientific Journals: Selecting Your Journal Medical Writing 30 10
Breaking the Code – Achieving Publication Success in Scientific Journals: The Essentials Medical Writing 23 3
CAPA (Corrective and Preventative Action) Regulatory Affairs 18 5
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 26-27 20-21
Cleaning Validation - Best Practice in Pharmaceuticals GxP 8-9 2-3
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 18-19 1-2
Clinical Quality Management Systems Clinical Research 22-23 18-19
Clinical Trial Monitoring Clinical Research 6-7 21-22 8-9
Clinical Trial Regulatory Requirements Clinical Research 8-9 15-16
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Clinical Research 17
Conflict Management for Pharmaceutical Executives Conflict Management 12-15 15-18 12-15
Cosmetovigilance Vigilance 19-20 13-14
Data Integrity Auditor Masterclass GxP 12-13 15-16
Data Integrity and Document Management GxP 7 14 11
Development of Combination Products: Critical Interactions GxP 24-25 2-3
Digital CMC: The Key To Realising Pharma 4.0 GxP 7 7 1
Digital Technology and Personalisation in Patient Support Programmes Clinical Research 2 5
Drafting Commercial Contracts for the Pharmaceutical Industry Commercial Contracts 21-22 12-13
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience Clinical Research 2-3 13-14
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 9-10 6-7
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 19 16
Effective Technical Writing & Editing Medical Writing 5 1
Effective Technology Transfer GxP 2-3 6-7
Effective Training Skills in the Pharma Industry Coaching & Mentoring 26-27 9-10
European Post-Marketing Pharmacovigilance Vigilance 14-16 3-7
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 1 21
GMP Principles in Vaccine Manufacturing GxP 16-17 10-11 10-11
Golden Rules of Being a Successful GMP Auditor GxP 2-3 1-2 5-6
Good Distribution Practices of Pharmaceuticals and APIs GxP 9-10 17-18
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 26-27 24-25 26-27
How to Deal with Difficult Situations in Audits GxP 4 6
How to Interview During Audits GxP 11 10
How to Manage Internal GMP Audits GxP 23-24 20-21 19-20
How to Pass International Health Authority Inspections GxP 19-20 8-9 12-13
How to Perform Bullet-Proof GDP and GSP Audits GxP 14-15 3-4
ICH Q9(R1) Quality Risk Management (QRM) GxP 12 17
Innovate: The MedTech Series – The 2024 EU AI Act Regulatory Affairs 3 2
Interpersonal Project Management Skills for the Life Sciences Industries Project Management 10-11 29-30 22-23
MBA Strategic Thinking for Pharma and Biopharma Professionals Leadership & Strategy 16-17 2-3
Making Financial Sense of GMP: Change Management GxP 11 14
Making Financial Sense of GMP: Pharmaceutical Quality System (PQS) GxP 13 3 13
Making Financial Sense of GMP: Quality Risk Management (QRM) GxP 27 7
Making Financial Sense of GMP: Validation Master Plan (VMP) GxP 20 10 27
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 23-24 16-17
Mastering Ethical and Effective Scientific Publishing: Applying Good Publication Practice (GPP) Medical Writing 25 14 20
Mastering Grant Writing: Essential Skills for Crafting Winning Proposals Medical Writing 10-11 9-10 13-14
Medical Writing Excellence: Crafting Compelling Scientific Documents Medical Writing 14-15 10-11 4-5
Medical Writing with Alex Evans: Medical Editing for Peer-Reviewed Journals Medical Writing 8 8
Medical Writing with Alex Evans: Medical Writing for Consumers Medical Writing 1 1
Medical Writing with Alex Evans: Medical Writing with Artificial Intelligence (AI) Medical Writing 29 15
Metrics and Earned Value in Clinical Research Projects Clinical Research 22 24
Microbiomics in Clinical Trials Clinical Research 4 14
Modern Agile Leadership for Pharma and Biopharma Professionals: Adapting to a Changing Workplace Leadership & Strategy 3-4 17-18
Molecular Biology for the Non-molecular Biologist Biopharma 25-26 3-4 9-10
Molecule to Medicine: An Introduction to Pharmacology in Drug Development Clinical Research 8 18
Molecule to Medicine: An Introduction to Signal Detection Vigilance 16 15 16
Molecule to Medicine: An Introduction to Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 4 12 5
Molecule to Medicine: An Introduction to the ‘Soft Side’ of Technology Transfers GxP 16 3 2
Navigating China’s API Regulations: An Essential Guide to DMF Registration GxP 23 23
Navigating ICH GCP E6 (R3): What You Need to Know Clinical Research 20 12 15
New EU GMP Annex 1: Compliant Aseptic Operations GxP 1-3 25-27
Pharmaceutical Development of ATMPs GxP 17-18 13-14
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 22-23 4-5
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 11-13 8-10
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 25-26 26-27
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 19-20 2-3
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 23-24 21-22
Pharmacovigilance Aspects of Licensing Agreements Vigilance 1 1-2
Pharmacovigilance QMS & Inspection Preparation Vigilance 19-20 25-26
Positive Persuading and Influencing Skills for Pharma Professionals Management 7-10 10-11
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 12-13 16-17
Process Validation with Qualification GxP 20-21 22-23
Project Management for Pharma Professionals Project Management 24-25 1-2
Protein Engineering for Pharmaceutical Biotechnology Biopharma 8-9 10-11 21-22
Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma Clinical Research 16 19
Regulatory Affairs for Support Staff Regulatory Affairs 12-13 22-23
Regulatory Strategies for Orphan Drugs Regulatory Affairs 23 7
Responsible Conduct of Research (RCR): Good Clinical Practice (GCP) GxP 12 8 2
Responsible Conduct of Research (RCR): Good Documentation Practice (GDocP) GxP 19 15 9
Responsible Conduct of Research (RCR): Good Publication Practice (GPP) GxP 9 29
Responsible Conduct of Research (RCR): Good Writing Practice (GWP) GxP 2 22 23
Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP) Vigilance 21 24
Risk Management for Clinical Research Clinical Research 6 7
Root Cause Analysis and Critical Thinking Management 15 24
Signal Detection and Regulatory Expectations Vigilance 7-8 18-21
Smart Packaging and Electronic Patient Information GxP 3 3-4
Software Automation in Research and Development (R&D) Clinical Trials Clinical Research 4 1
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 21-22 10-11
Successful Medical Writing – from Protocol to CTD Medical Writing 5-6 25-26
The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries Biopharma 9-10 12-13
The Common Technical Document GxP 7-8 24-25
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 1 28
The FDA Drug Approval Process Regulatory Affairs 11-12 7-8
The Leadership and Management Summer School for Pharma Professionals Leadership & Strategy 7-11
The Pharma Mini MBA Leadership & Strategy 19-21 9-11 5-7
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 12-13 13-14
Thinking Outside of the GMP Box GxP 13-14 17-18
US FDA - Understanding Key Factors When Working with the FDA Biopharma 11 26
Understanding Active Pharmaceutical Ingredients (APIs) GxP 16-17 19-20
Understanding Computer System Validation (CSV) GxP 9-10 24-25
Understanding Pharmacovigilance Regulations in APAC Vigilance 16-17 9-10
Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes Clinical Research 18 15
Variations to Marketing Authorisations Regulatory Affairs 3-4 15-16
Working with Emotional Intelligence in the Pharmaceutical and Biopharma Industry Leadership & Strategy 30 20