Pharmaceutical Training Course Calendar

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Our Pharmaceutical calendar for the next 12 months:

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