Life Sciences Training Course Calendar

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Our Life Sciences calendar for the next 12 months:

Live online Classroom 2024 2025
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 5 1
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 13-14
A Practical Guide to Producing and Maintaining the PSMF Vigilance 14 23 3
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 5 21 11
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China Regulatory Affairs 2-3
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 21
AI in Pharmacovigilance Vigilance 12 7
Additional Risk Minimization Measures (aRMMs) and Their Effectiveness Vigilance 4 9 10
Advanced Pharmacovigilance Vigilance 9-13 24-26 2-4 6-10
Advanced Project Management in Clinical Research Clinical Research 11 9 3
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 13-14 3-4 2-3
Advanced Veterinary Pharmacovigilance Vigilance 13-14 24-25 15-16
An Essential Overview of Medical Information Regulatory Affairs 29 14 18
An Essential Overview of Pharmacovigilance Vigilance 27 15 8-9
An Essential Overview of the Medical Device Industry Regulatory Affairs 14 3
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 16 12 22
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 11 1
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 17 9
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 22
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 13 3
An Introduction to Pharmaceutical Packaging GxP 13-15 2-4 24-26
An Introduction to the Design and Development of Medical Devices Medical Technology 10-11 8-9 23-24
An Introduction to the Medical Device Regulation Regulatory Affairs 25-27 16-18
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 11
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 27 26 23
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions Regulatory Affairs 9 17
Best Practice for Writing Effective SOPs Regulatory Affairs 12 27 17
Best Practices for Supplier Qualification in Life Science GxP 7-8 27-28 16-17
Biological Evaluation of Medical Devices Regulatory Affairs 15-16 15-16 15-16
Biosimilars Biopharma 30-31 21-22 30-1
Biotechnology for the Non-Biotechnologist Biopharma 2-6
Building Better Health via Digitalised and Personalised Patient Support Programmes Clinical Research 12 2
CAPA (Corrective and Preventative Action) Regulatory Affairs 13 28 18
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 27-28 26-27 20-21
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 28 9
Cleaning Validation Best Practice in Pharmaceuticals GxP 5-6 8-9 8-9
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 22 13 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 27-28 31-3 21-22
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 5-6 18-19 1-2
Clinical Quality Management Systems Clinical Research 23-24 22-23 18-19
Clinical Research Project Management Clinical Research 29-31 11-13 22-24
Clinical Trial Monitoring Clinical Research 2-3 28-29 21-22
Clinical Trial Regulatory Requirements Clinical Research 20-21 8-9 15-16
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Clinical Research 19 17
Cosmetovigilance Vigilance 3-4 19-20 13-14
Cyber Security for Medical Devices Regulatory Affairs 28-29 8-9 11-12
Data Innovation for AI-enabled Medical Devices Regulatory Affairs 28 9
Data Integrity Auditor Masterclass GxP 4-5 12-13 15-16
Data Integrity and Document Management GxP 6 7 14
Deep Dive into the IVDR Annex XIII Regulatory Affairs 5 10
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 3 10
Development of Combination Products: Critical Interactions GxP 10-11 24-25 2-3
Drug Discovery: A Step-by-Step Introduction Medical Technology 23-24 8-9 18-19
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience Clinical Research 13-14 2-3 13-14
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 10-11 9-10 6-7
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 20 19 16
Effective Technical Writing & Editing Medical Writing 5 5 1
Effective Technology Transfer GxP 3-4 2-3 6-7
European Post Marketing Pharmacovigilance - Including the EMA/PRAC Deliberations and Brexit Implications Vigilance 3-7 14-16
FDA Approval Process for Medical Devices Regulatory Affairs 2-3 31-1 22-23
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 22 14 1
GMP Principles in Vaccine Manufacturing GxP 16-17 10-11
Global Pharmaceutical Regulatory Affairs Summer School Regulatory Affairs 9-13
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18 9-10
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 15-16 13-14 16-17
ICH Q9(R1) Quality Risk Management (QRM) GxP 29 12 9
Introduction to Good Clinical Practice (GCP) GxP 11-12 24-25 7-8
Introduction to Veterinary Pharmacovigilance Vigilance 10-11 3-4
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 5-6 16-17
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746) Regulatory Affairs 4 9
Managing Competence within the Medical Device Industry Regulatory Affairs 26 11
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 6-7 23-24 16-17
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 26-27 7-8
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 7
Masterclass: Market Authorisation of AI-enabled Medical Devices Regulatory Affairs 4 11
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 9-10 3-4 23-24
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 10-11 23-24
Medical Device Single Audit Programme (MDSAP) GxP 28-29 24-25 10-11
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 18-21
Medical Device Studies: Clinical Evidence Clinical Research 17-18 9-10
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 15-16 7-8 15-16
Medical Writing for Medical Devices Medical Writing 25-26 1-2
Metered Dose Inhaler (MDI) Technology Medical Technology 24-27 19-20 8-9
Metrics and Earned Value in Clinical Research Projects Clinical Research 25 5 22
Microbiomics in Clinical Trials Clinical Research 27 4 14
Navigating China’s API Regulations: An Essential Guide to DMF Registration GxP 12 23 23
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 21-22 19-20 10-11
Navigating Regulatory Compliance Whilst Developing and Distributing PCR-Based IVD Tests Regulatory Affairs 6 26
New EU GMP Annex 1: Compliant Aseptic Operations GxP 26-28 11-13 1-3
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 12 10 18
Pharmaceutical Development of ATMPs GxP 3-4 17-18 13-14
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 19-20 24-25 16-17 21-22
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 25-27 11-13 8-10
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 10-11 31-1 25-26
Pharmaceutical Regulatory Affairs in Latin America Regulatory Affairs 25 18 22
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 6-7 19-20 2-3
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 9-10 25-26 23-24 21-22
Pharmacovigilance Vigilance 5-7 11-13 15-17
Pharmacovigilance Aspects of Licensing Agreements Vigilance 27-28 10 1
Pharmacovigilance QMS & Inspection Preparation Vigilance 20-21 19-20 25-26
Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors – Broadening your Knowledge Vigilance 29-31 7-9 29-1
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 12 5 9
Practical Implementation of GCP in Veterinary Field Studies GxP 26-27 14-15
Practical Implementation of a Human Factors Study Regulatory Affairs 4-5 1-2
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 10-11 12-13 16-17
Pre-Filled Syringes: End-to-End Processing Medical Technology 6-7 20-21 21-22
Process Validation for Medical Devices GxP 25-26 5-6 22-23
Process Validation with Qualification GxP 13-14 20-21 22-23
Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in The Pharmaceutical Market Clinical Research 26 16
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs 27 26 23
Regulatory Affairs for Support Staff Regulatory Affairs 27-28 12-13 22-23
Regulatory Strategies for Orphan Drugs Regulatory Affairs 10 23 7
Risk Evaluation and Mitigation Strategies (REMS) vs Risk Management Plans (RMP) Vigilance 15 21 24
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 4 6 7
Signal Detection and Regulatory Expectations Vigilance 12-15 17-18 7-8
Smart Packaging and Electronic Patient Information GxP 4-5 13 2
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 11-12 24-27 21-22
Sterilization of Medical Devices GxP 3-4 5-6 16-17
Successful Medical Writing – from Protocol to CTD Medical Writing 16-17 5-6 25-26
Sustainable Design and Manufacture for Medical Devices Medical Technology 24 3
The Advancement of Research and Development (R&D) Clinical Trials using Software Automation Clinical Research 12 4 1
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 16-19
The Common Technical Document GxP 25-26 11-12 7-8
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 28 13 1
The FDA Drug Approval Process Regulatory Affairs 2-3 24-25 11-12 7-8
The Importance of Patient Adherence Data and How Digital Tools Can Improve Patient Outcomes Clinical Research 26 18 15
The Medical Device School - From Concept to CE Marking Regulatory Affairs 2-6 9-13
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 13-14 12-13 13-14
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 23 22 22
Thinking Outside of the GMP Box GxP 14-15 13-14 17-18
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 10 26 21
US FDA - Understanding Key Factors When Working with the FDA Biopharma 27 13 11
Understanding Active Pharmaceutical Ingredients (APIs) GxP 25-26 16-17
Understanding Computer System Validation (CSV) GxP 18-19 9-10
Understanding Pharmacovigilance Regulations in APAC Vigilance 13-14 16-17 9-10
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 5 24 8
Variations to Marketing Authorisations Regulatory Affairs 28-29 6-7 3-4 15-16
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 26-27 19-20