Industry Training Course Calendar

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Our Industry calendar for the next 12 months:

Live online Live online Classroom 2024 2025
Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 4 5
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 5
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 8-9 11-12
A Practical Guide to Producing and Maintaining the PSMF Vigilance 24 5 10
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 1 9
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 22
Advanced Pharmacovigilance Vigilance 5-7 18-20 9-13
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 4-7 7-8
Advanced Reinsurance Contracts and Disputes Masterclass Contract Wordings 11 2
Advanced Understanding and Drafting Oil and Gas Industry Contracts Commercial Contracts 10 23 18-19
Advanced Veterinary Pharmacovigilance Vigilance 30-1 2-3 9-10
Agile Leadership for Pharma and Biopharma Professionals in a hybrid world Leadership & Strategy 4-5 18-19
An Essential Overview of Medical Information Regulatory Affairs 11 29
An Essential Overview of Pharmacovigilance Vigilance 16 9-10
An Essential Overview of the Medical Device Industry Regulatory Affairs 8-9 8
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 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 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 4 20
An Introduction to ISO 22716 - GMP for Cosmetic Products GxP 17-18 19-22
An Introduction to Pharmaceutical Packaging GxP 20-22 25-27
An Introduction to the Design and Development of Medical Devices Medical Technology 22-23 24-25 10-11
An Introduction to the Medical Device Regulation Regulatory Affairs 15-17 31-2 4-6
Best Practice for Writing Effective SOPs Regulatory Affairs 23 18 12
Biological Evaluation of Medical Devices Regulatory Affairs 16-17
Biosimilars Biopharma 10-11 1-2
Biotechnology for the Non-Biotechnologist Biopharma 24-28 25-27 2-6
CAPA (Corrective and Preventative Action) Regulatory Affairs 22 19 13
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 27-28 17-18
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 9-10 5-6 27-28
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 19-20 2-3
Clinical Quality Management Systems Clinical Research 23-24 19-20
Clinical Research - A Different Approach to Successful Project Delivery Clinical Research 10 4
Clinical Trial Monitoring Clinical Research 29-30 11-12 2-3
Clinical Trial Regulatory Requirements Clinical Research 2-3 16-17
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Clinical Research 18
Consultative Selling for Pharma Professionals Sales 13-14 17-18
Cosmetovigilance Vigilance 20-21 14-15
Cyber Security for Medical Devices Regulatory Affairs 2-3 4-5 15-16
Data Integrity Auditor Master Class GxP 30-1 24-25 16-17
Data Integrity and Document Management GxP 22 6
Delivery of Biologics to the Nasal Cavity Biopharma 4 8
Development of Combination Products: Critical Interactions GxP 25-26 3-4
Drafting Commercial Contracts for the Pharmaceutical Industry Commercial Contracts 8-9 20-21
Drafting and Negotiating Clinical Trial Agreements Commercial Contracts 9 19 5
Drug Discovery: A Step-by-Step Introduction Medical Technology 9-10 19-20
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience Clinical Research 20-21 25-26 11-12
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 10-11 14-15
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 22 18
Effective Technical Writing & Editing Medical Writing 28 1
Effective Technology Transfer GxP 16-17 7-8
Effective Training Skills in the Pharma Industry Coaching & Mentoring 13-14 10-11
European Post Marketing Pharmacovigilance - Including the EMA/PRAC Deliberations and Brexit Implications Vigilance 15-17 4-8
FDA Approval Process for Medical Devices Regulatory Affairs 19-20 10-11 2-3
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 1 22
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 17-20 5-6
ICH Q9(R1) Quality Risk Management (QRM) GxP 1 25
Introduction to Veterinary Pharmacovigilance Vigilance 26-27 2-3
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 24-25 5-8
MBA Strategic Thinking for Pharma and Biopharma Professionals Leadership & Strategy 25-26 3-4
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 18-19 24-25 17-18
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 26 7
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 16-19 2-3 9-10
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 11-12 7-8
Medical Device Single Audit Programme (MDSAP) GxP 4-5 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 22-25 22-25 9-12
Medical Device Studies: Clinical Evidence Clinical Research 10-11 11-12
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 21-22 16-19
Medical Writing for Medical Devices Medical Writing 1-2 21-22
Metered Dose Inhaler (MDI) Technology Medical Technology 20-21 9-10
Metrics and Earned Value in Clinical Research Projects Clinical Research 11 25
New EU GMP Annex 1: Compliant Aseptic Operations GxP 2-4 26-28
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 19 12
Pharmaceutical Development of ATMPs GxP 18-19 14-15
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 17-18 19-22
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 12-14 9-11
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 29-30 2-3 10-11
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 24-25 3-4
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 22-23 26-27 9-10
Pharmacovigilance Vigilance 12-14 9-11
Pharmacovigilance Aspects of Licensing Agreements Vigilance 10 27-28
Pharmacovigilance QMS & Inspection Preparation Vigilance 20-21 26-27
Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors - Broadening your Knowledge Vigilance 8-10 30-2
Positive Persuading and Influencing Skills for Pharma Professionals Management 29-30 11-12
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 6 10
Practical Implementation of GCP in Veterinary Field Studies GxP 15-16 26-27
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 13-14 17-18
Pre-Filled Syringes: End-to-End Processing Medical Technology 25-26 6-7
Process Validation for Medical Devices GxP 5-6 15-16
Process Validation with Qualification GxP 21-22 23-24
Project Management for Pharma Professionals Project Management 17-18 26-27 9-10
Regulatory Affairs for Support Staff Regulatory Affairs 13-14 24-25
Regulatory Strategies for Orphan Drugs Regulatory Affairs 24 8
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 7 8
Root Cause Analysis and Critical Thinking Management 23 25
Signal Detection and Regulatory Expectations Vigilance 1-2 12-15
Smart Packaging and Electronic Patient Information GxP 10 4-5
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 11-12 11-12
Sterilization of Medical Devices GxP 6-7 17-18
Successful Medical Writing – from Protocol to CTD Medical Writing 27-29
Sustainable Design and Manufacture for Medical Devices Medical Technology 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 8-9 25-26
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 10 28
The FDA Drug Approval Process Regulatory Affairs 12-13 2-3
The Leadership and Management Summer School for Pharma Professionals Leadership & Strategy 29-2
The Medical Device School - From Concept to CE Marking Regulatory Affairs 10-14 2-6
The Pharma Mini MBA Leadership & Strategy 15-17 31-2 6-8
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 21 24
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 19
US FDA - Understanding Key Factors When Working with the FDA Biopharma 12 27
Understanding Active Pharmaceutical Ingredients (APIs) GxP 17-18 18-19
Understanding Computer System Validation (CSV) GxP 24-25 25-26
Understanding Pharmacovigilance Regulations in APAC Vigilance 23-24 8-9 8-9
Understanding and Drafting Oil and Gas Industry Contracts Commercial Contracts 22 15-16
Understanding and Interpreting the Proposed Changes to EU GMP Annex 11 GxP 14 17 21
Understanding the Reinsurance Industry Contract Wordings 2-3 6-7
Variations to Marketing Authorisations Regulatory Affairs 4-5 28-29
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 11-12 26-27
Working with Emotional Intelligence in the Pharmaceutical and Biopharma Industry Leadership & Strategy 21 14