Life Sciences Training Course Calendar

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Our Life Sciences calendar for the next 12 months:

Live online Classroom 2025 2026
Sep Oct Nov Dec Jan Mar Mar Apr May Jun Jul Aug
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 4 7
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 6-7 10-11 10-11
A Practical Guide to Producing and Maintaining the PSMF Vigilance 3
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 12 20 20
A Practical Introduction to Good Clinical Practice (GCP) GxP 15
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 21 29
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 3 2 2
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 9-10 23-25 23-25
Advanced Veterinary Pharmacovigilance Vigilance 15-16 21-22
An Essential Overview of Medical Information Regulatory Affairs 4 22
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 12 12
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 10 14
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 20 8
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 17
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 20 21
An Introduction to Signal Detection Vigilance 15 16
An Introduction to Technology Transfer for Solid Dosage Forms GxP 14 6 6
An Introduction to the Design and Development of Medical Devices Medical Technology 10-11 29-30
An Introduction to the Medical Device Regulation Regulatory Affairs 3-5
An Overview of Ethical Standards in Clinical Research Publication GxP 13
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 27
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 23 16
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
Best Practice for Writing Effective SOPs Regulatory Affairs 4 26 26 14
Best Practices for Supplier Qualification in Life Science GxP 13-14 6-7
Biological Evaluation of Medical Devices Regulatory Affairs 21-22 13-14
Biosimilars Biopharma 30-1 16-17 16-17
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
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 12
Cleaning Validation - Best Practice in Pharmaceuticals GxP 2-3 23-24
Cleanroom Requirements for Medical Device Manufacturers Regulatory Affairs
Clinical & Post-Marketing Safety Vigilance 11-12
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 28
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 25-26
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 16-17 16-17
Clinical Quality Management Systems Clinical Research 23-24 23-24
Clinical Research Project Management Clinical Research 22-24 29-1
Clinical Trial Monitoring Clinical Research 29-30
Clinical Trial Regulatory Requirements Clinical Research 2-3 2-3
Cosmetovigilance Vigilance 13-14 18-19
Cyber Security for Medical Devices Regulatory Affairs 19-20 19-20
Data Innovation for AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 12
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
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 13
Development of Combination Products: Critical Interactions GxP
Digital CMC Medical Technology 6
Digital CMC: The Key To Realising Pharma 4.0 GxP 1 23
Digital Technology Transfers Medical Technology 4 4
Digital Technology and Personalisation in Patient Support Programmes Clinical Research 5 6
EU Pharmaceutical Regulations and Strategy Regulatory Affairs 2-3 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 3 18
Effective Deviation Management Systems in Pharma GxP 20 20
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 21 15
Effective Technical Writing & Editing Medical Writing 30 15
Effective Technology Transfer GxP 6-7
Ensuring Clinical Research Quality & Patient Safety GxP
Essential Documentation Skills for Clinical Research Compliance GxP 9 9
FDA Approval Process for Medical Devices Regulatory Affairs 2-3 30-1
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 21 19
GMP Principles in Vaccine Manufacturing GxP 10-11 16-17
Global Market Access for Medical Device Software Regulatory Affairs 1-2 8-9
Golden Rules of Being a Successful GMP Auditor GxP
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
How to Deal with Difficult Situations in GMP Audits GxP 6 5 5
How to Interview During GMP Audits GxP 10 12 12
How to Manage Internal GMP Audits GxP 20-21
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
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs
Introduction to Veterinary Pharmacovigilance Vigilance 5-6 9-10 9-10
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17
Literature Searching in Drug Safety Vigilance 19-20
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 16-17 13-14
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 10-11
Masterclass: Market Authorisation of AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 18-19 29-30
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 Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 9-10 30-1
Medical Device Regulations in Asia-Pacific Markets Regulatory Affairs 3-4 3-4 3-4
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 19-20 18-19
Medical Device Single Audit Programme (MDSAP) GxP 26-27 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 26-30 22-26
Medical Device Studies: Clinical Evidence Clinical Research 15-16
Medical Editing for Peer-Reviewed Journals Medical Writing 8
Medical Writing Excellence: Crafting Compelling Scientific Documents Medical Writing
Medical Writing for Consumers Medical Writing 21
Medical Writing for Medical Devices Medical Writing 20-21 25-26
Medical Writing with AI Artificial Intelligence (AI) in Life Sciences 15 18
Metered Dose Inhaler (MDI) Technology Medical Technology 27-28
Metrics and Earned Value in Clinical Research Projects Clinical Research 24 6
Microbiomics in Clinical Trials Clinical Research
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 2-3
Navigating ICH GCP E6 (R3): What You Need to Know Clinical Research 29 13
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Regulatory Affairs 6 15
New EU GMP Annex 1: Compliant Aseptic Operations GxP 25-27 19-21
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 11 19
Orphan Drug Regulatory Masterclass: EU & US Insights Regulatory Affairs 14 4 4
Overview of EU and UK Regulatory Affairs Regulatory Affairs
Pharmaceutical Development of ATMPs GxP 13-14 18-19 18-19
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 8-10
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 26-27 12-13
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 5-6 5-6
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs
Pharmaceutical Regulatory Affairs in the Middle East and North Africa Regulatory Affairs 21-23
Pharmacovigilance Aspects of Licensing Agreements Vigilance 1-2 25
Pharmacovigilance QMS & Inspection Preparation Vigilance 25-26 27-28
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection Vigilance 30
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Vigilance 3-4 10-11
Practical Implementation of GCP in Veterinary Field Studies GxP 25-26 13-14
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 21-22
Pre-Filled Syringes: End-to-End Processing Medical Technology 5-6 11-12
Process Validation for Medical Devices GxP 22-23 4-5
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
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs 23 16
Regulatory Compliance and Safety Standards for Aesthetic Devices Regulatory Affairs 5 12
Selecting the Best Scientific Journal for Your Research Medical Writing 10 13
Signal Detection and Regulatory Expectations Vigilance 18-21
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 17
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 10-11 20-21
Sterilization of Medical Devices GxP 16-17 23-24
Successful Cognitive Testing in Clinical Drug Trials: Biomarkers, Test Selection & Integration Clinical Research 16 16
Successful Medical Writing – from Protocol to CTD Medical Writing 23-24 23-24
Sustainable Product Design for MedTech Engineers and Developers Medical Technology 27 7
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 23
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 15-18
The Applications of Nanoparticles in the Pharmaceutical and Biomedical Industries Biopharma 12-13 11-12 11-12
The Common Technical Document GxP 24-25 27-28 14-15
The FDA Drug Approval Process Regulatory Affairs 7-8
The Financial Benefits of Change Management GxP 13
The Financial Benefits of Pharmaceutical Quality Systems GxP
The Financial Benefits of Quality Risk Management GxP 17
The Financial Benefits of Validation Master Plans GxP 6 6
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 10 17
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 13-14 20-21
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 4 4
Thinking Outside of the GMP Box GxP
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 21 15
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
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 20 8
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 15-16 2-3
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 25-26 18-19