Life Sciences Training Course Calendar

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Our Life Sciences calendar for the next 12 months:

Live online Classroom 2023 2024
Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 4
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 18 5
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 11-12 11-12
A Practical Guide to Producing and Maintaining the PSMF Vigilance 19 24 5 10
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 18 16 1 9
Advanced Pharmacovigilance Vigilance 11-15 20-22 5-7 18-20
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 1-2 4-7 7-8
Advanced Veterinary Pharmacovigilance Vigilance 22-25 16-17 18-19 16-17
An Essential Overview of Medical Information Regulatory Affairs 15 11 29
An Essential Overview of Pharmacovigilance Vigilance 29 16 9-10
An Essential Overview of the Medical Device Industry Regulatory Affairs 1 8-9 8
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 19 10 13
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 1 11
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 24 10 23
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 21 18
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 6 4 20
An Introduction to ISO 22716 - GMP for Cosmetic Products GxP 19-20 17-18 19-22
An Introduction to Pharmaceutical Packaging GxP 30-1 20-22 25-27
An Introduction to the Design and Development of Medical Devices Medical Technology 22-23 24-25
An Introduction to the Medical Device Regulation Regulatory Affairs 6-8 15-17 31-2 4-6
Artificial Intelligence and Machine Learning Powered Signal Management Medical Technology 24 15 18
Best Practice for Writing Effective SOPs Regulatory Affairs 14 23 18
Biological Evaluation of Medical Devices Regulatory Affairs 11-12 16-17
Biosimilars Biopharma 5-6 10-11 1-2
Biotechnology for the Non-Biotechnologist Biopharma 24-26 24-28 25-27
CAPA (Corrective and Preventative Action) Regulatory Affairs 22 19
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 29-1 27-28 17-18
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 26-29 9-10 5-6 27-28
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 7-8 19-20 2-3
Clinical Quality Management Systems Clinical Research 25-26 23-24 19-20
Clinical Research - A Different Approach to Successful Project Delivery Clinical Research 16 10 4
Clinical Research Project Management Clinical Research 26-28 26-28 23-25
Clinical Trial Monitoring Clinical Research 29-30 11-12
Clinical Trial Regulatory Requirements Clinical Research 22-23 2-3 16-17
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Clinical Research 20 18
Cosmetovigilance Vigilance 5-6 20-21 14-15
Cyber Security for Medical Devices Regulatory Affairs 30-31 2-3 4-5 15-16
Data Integrity Auditor Master Class GxP 30-31 30-1 24-25 16-17
Data Integrity and Document Management GxP 12 22
Delivery of Biologics to the Nasal Cavity Biopharma 6 4 8
Development of Combination Products: Critical Interactions GxP 12-13 25-26 7-10
Drug Discovery: A Step-by-Step Introduction Medical Technology 25-26 9-10 19-20
Drug/Device and Device/Drug Combinations in the EU and USA Regulatory Affairs 14-15 17-18
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience Clinical Research 15-16 20-21 25-26 11-12
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 12-13 11-12 14-15
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 24 22 18
Effective Technical Writing & Editing Medical Writing 1 28 1
Effective Technology Transfer GxP 23-24 16-17 16-17 7-8
European Post Marketing Pharmacovigilance - Including the EMA/PRAC Deliberations and Brexit Implications Vigilance 4-8 15-17 4-8
FDA Approval Process for Medical Devices Regulatory Affairs 4-7 19-20 10-11
Filing eCTD Submissions Regulatory Affairs 25 19
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 15 1 22
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 5-6 17-20
ICH Q9(R1) Quality Risk Management (QRM) GxP 31 1 25
In the Light of Annex 1: Use of Barrier Systems for Aseptic Pharmaceutical Manufacturing GxP 6
Introduction to Veterinary Pharmacovigilance Vigilance 5-8 27-28 2-3
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 7-8 24-25 5-8
Managing Competence within the Medical Device Industry Regulatory Affairs 1 5
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Clinical Research 15-16 18-19 24-25 17-18
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 6 26 7
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 11-12 16-19 2-3
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 5-6 11-12 7-8
Medical Device Single Audit Programme (MDSAP) GxP 25-26 4-5 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 11-14 22-25 22-25
Medical Device Studies: Clinical Evidence Clinical Research 18-21 10-11 11-12
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 17-18 21-22 16-19
Medical Writing for Medical Devices Medical Writing 13-14 1-2 21-22
Metered Dose Inhaler (MDI) Technology Medical Technology 26-29 20-21 9-10
Metrics and Earned Value in Clinical Research Projects Clinical Research 6 11 25
Navigating China’s API Regulations: An Essential Guide to DMF Registration GxP 1
New EU GMP Annex 1: Compliant Aseptic Operations GxP 12-14 2-4 26-28
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 19
Pharmaceutical Development of ATMPs GxP 5-8 18-19 14-15
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 7-8 23-24 19-22
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 27-29 12-14 9-11
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 12-13 29-30 2-3
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 8-9 24-27 3-4
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 22-23 17-18
Pharmacovigilance Vigilance 31-2 12-14 9-11
Pharmacovigilance Aspects of Licensing Agreements Vigilance 1 10 27-28
Pharmacovigilance QMS & Inspection Preparation Vigilance 22-25 20-21 26-27
Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors - Broadening your Knowledge Vigilance 31-2 8-10 30-2
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Vigilance 14 6 10
Practical Implementation of GCP in Veterinary Field Studies GxP 19-20 26-27
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 13-14 13-14 17-18
Pre-Filled Syringes: End-to-End Processing Medical Technology 21-22 25-26 6-7
Process Validation for Medical Devices GxP 7-8 5-6 15-16
Process Validation with Qualification GxP 16-17 21-22 23-24
Registration of Veterinary Vaccines in the USA and Canada Regulatory Affairs 1-2 11-12
Regulatory Affairs for Support Staff Regulatory Affairs 29-30 13-14 24-25
Regulatory Strategies for Orphan Drugs Regulatory Affairs 15 24 8
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 2 7 8
Robotics and Digitalization in Aseptic Pharmaceutical Manufacturing GxP 14
Signal Detection and Regulatory Expectations Vigilance 18-19 1-2 12-15
Smart Packaging and Electronic Patient Information GxP 14 10 4-5
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 4-7 11-12 11-12
Sterilization of Medical Devices GxP 1-2 6-7 17-18
Successful Medical Writing – from Protocol to CTD Medical Writing 20-22 24-26 27-29
Sustainable Design and Manufacture for Medical Devices Medical Technology 23 25 4 4
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 17-20
The Common Technical Document GxP 12-13 2-3 25-26
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 14 10 28
The FDA Drug Approval Process Regulatory Affairs 6-7 12-13 14-15
The Medical Device School - From Concept to CE Marking Regulatory Affairs 10-14
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 24 21 24
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 1 15 19
US FDA - Understanding Key Factors When Working with the FDA Biopharma 19 18 19
Understanding Active Pharmaceutical Ingredients (APIs) - A Comprehensive and Practical Introduction GxP 13-14 17-18 18-19
Understanding Computer System Validation (CSV) - A Comprehensive and Practical Introduction GxP 19-20 24-25 25-26
Understanding Pharmacovigilance Regulations in APAC Vigilance 23-24 23-24 8-9 8-9
Variations to Marketing Authorisations Regulatory Affairs 1-2 4-5 10-11
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 12-13 4-5 26-27