Pharmaceutical Training Course Calendar

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Our Pharmaceutical calendar for the next 12 months:

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