Life Sciences Training Course Calendar

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Our Life Sciences calendar for the next 12 months:

Live online Classroom 2025 2026
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Journey Through Innovation to an AI-Driven Future Artificial Intelligence (AI) in Life Sciences 7 14
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 23-24
A Practical Guide to Producing and Maintaining the PSMF Vigilance 13 29
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 12 20 16
A Practical Introduction to Good Clinical Practice (GCP) GxP 15 6
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 29 20
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 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
Advanced Project Management in Clinical Research Clinical Research
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs
Advanced Veterinary Pharmacovigilance Vigilance 21-22
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 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 19 21
An Introduction to Pharmaceutical Packaging GxP 26-28 6-8
An Introduction to Signal Detection Vigilance 16 14
An Introduction to Technology Transfer for Solid Dosage Forms GxP 14 6 18
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 introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 27 20
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 16 22
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 23
Best Practice for Writing Effective SOPs Regulatory Affairs 4 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 16-17 22-23
Biotechnology for the Non-Biotechnologist Biopharma 10-14
Building The Business Case For Pharma 4.0 Medical Technology 13 6
CAPA (Corrective and Preventative Action) Regulatory Affairs 5 15
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 23-24 19-20
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 23 21
Clinical & Post-Marketing Safety Vigilance 11-12
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 28 1
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 30-1
Clinical Quality Management Systems Clinical Research 23-24 17-18
Clinical Research Project Management Clinical Research 29-1 21-23
Clinical Trial Monitoring Clinical Research 29-30
Clinical Trial Regulatory Requirements Clinical Research 2-3 14-15
Conducting Clinical Research With Integrity GxP 2 14
Cosmetovigilance Vigilance 18-19
Cyber Security for Medical Devices Regulatory Affairs 19-20 28-29
Data Innovation for AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 12
Data Integrity Auditor Masterclass GxP 22-23 14-15
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 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 5 6
Documenting Clinical Research with Integrity GxP 9 5
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience Clinical Research
EU Pharmaceutical Regulations and Strategy Regulatory Affairs 2-3 5-6
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 15
Effective Deviation Management Systems in Pharma GxP 20
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 21 15
Effective Technical Writing & Editing Medical Writing 15
Effective Technology Transfer GxP
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 5-6 30-1
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18 14-15
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 26-27 14-15
How to Deal with Difficult Situations in GMP Audits GxP 6 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 7-8
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 11-12 15-16
Introduction to Veterinary Pharmacovigilance Vigilance 5-6 9-10 16-17
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 4-5 16-17 15-16
Literature Searching in Drug Safety Vigilance 19-20
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 13-14 15-16
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 19-20
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 4-5 3-4 16-17
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 Studies: Clinical Evidence Clinical Research
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 1
Medical Writing for Medical Devices Medical Writing 20-21 25-26
Medical Writing with AI Artificial Intelligence (AI) in Life Sciences 18
Metered Dose Inhaler (MDI) Technology Medical Technology 27-28 7-8
Metrics and Earned Value in Clinical Research Projects Clinical Research 24 6
Microbiomics in Clinical Trials Clinical Research 26 14
Molecular Biology for the Non-Molecular Biologist Biopharma 20-21 8-9
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
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 4 6
Overview of EU and UK Regulatory Affairs Regulatory Affairs 11-12 21-22
Pharmaceutical Development of ATMPs GxP 18-19 28-29
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 4-5 6-7
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 24-26 7-9
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 20-21
Pharmaceutical Regulatory Affairs in the Middle East and North Africa Regulatory Affairs
Pharmacovigilance Aspects of Licensing Agreements Vigilance 1-2 25
Pharmacovigilance QMS & Inspection Preparation Vigilance 27-28 8-9
Pharmacovigilance: An Overview of Drug Safety from Safety Collection to Regulatory Inspection Vigilance 30 5-6
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 12-13
Pre-Filled Syringes: End-to-End Processing Medical Technology 5-6 11-12
Process Validation for Medical Devices GxP 4-5
Process Validation with Qualification GxP
Protein Engineering for Pharmaceutical Biotechnology Biopharma 21-22 7-8
Publishing Clinical Research with Integrity GxP 13
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 16 22
Regulatory Compliance and Safety Standards for Aesthetic Devices Regulatory Affairs 5 12
Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP) Vigilance
Risk Management for Clinical Research Clinical Research
Selecting the Best Scientific Journal for Your Research Medical Writing 10 13 19
Signal Detection and Regulatory Expectations Vigilance 18-21 2-3 30-1
Signal Detection: A Comprehensive Introduction Vigilance 28 13 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
Sterilization of Medical Devices GxP 23-24 15-16
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
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 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 21-22
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 28 19
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 9
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 10 17
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 20-21 12-13
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 4 21
Thinking Outside of the GMP Box GxP 3-4 16-17
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 21
US FDA - Understanding Key Factors When Working with the FDA Biopharma 26 12
Understanding Active Pharmaceutical Ingredients (APIs) GxP 19-20 29-30 21-22
Understanding Computer System Validation (CSV) GxP 24-25 17-18
Understanding Scientific Journal Submission and Publication Medical Writing 17 11
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 13
Variations to Marketing Authorisations Regulatory Affairs 2-3
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 25-26 18-19
Writing Clinical Research with Integrity GxP 20