Pharmaceutical Training Course Calendar

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Our Pharmaceutical calendar for the next 12 months:

Live online Classroom 2023 2024
Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May
A Practical Guide to Producing and Maintaining the PSMF Vigilance 25 6
A Practical Guide to Writing Risk Management Plans (RMPs) Vigilance 24 5
Advanced Pharmacovigilance Vigilance 20-22 11-15
Agile Leadership for Pharma and Biopharma Professionals in a hybrid world Leadership & Strategy 6-7 20-21
An Essential Overview of Medical Information Regulatory Affairs 1
An Essential Overview of Pharmacovigilance Vigilance 11-12
An Essential Overview of the Medical Device Industry Regulatory Affairs 10-11 10
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 15
An Introduction to Pharmaceutical Packaging GxP 27-29
Artificial Intelligence and Machine Learning Powered Signal Management Medical Technology 20 24 15
Best Practice for Writing Effective SOPs Regulatory Affairs 17 14
Biosimilars Biopharma 12-13 30-31
Biotechnology for the Non-Biotechnologist Biopharma 26-30 27-29 4-8
CAPA (Corrective and Preventative Action) Regulatory Affairs 18 15
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 6-7 26-27
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 28-29 4-5
Clinical Quality Management Systems Clinical Research 16-17
Clinical Research - A Different Approach to Successful Project Delivery Clinical Research 6
Clinical Trial Monitoring Clinical Research 9-10
Clinical Trial Regulatory Requirements Clinical Research 18-19
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Clinical Research 20 20
Consultative Selling for Pharma Professionals Sales 19-20
Cosmetovigilance Vigilance 9-10
Data Integrity and Document Management GxP 24 1
Delivery of Biologics to the Nasal Cavity Biopharma 10
Development of Combination Products: Critical Interactions GxP 27-28 9-12
Drafting Commercial Contracts for the Pharmaceutical Industry Commercial Contracts 10-11 22-23
Drafting and Negotiating Clinical Trial Agreements Commercial Contracts 21 7
Drug Discovery: A Step-by-Step Introduction Medical Technology 21-22
EU Clinical Trial Regulation 536/2014: Overview and Implementation Clinical Research 20-21 13-14
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 16-17
Effective Technical Writing & Editing Medical Writing 30 3
Effective Technology Transfer GxP 18-19 12-13
Effective Training Skills in the Pharma Industry Coaching & Mentoring 27-28 16-17
European Post Marketing Pharmacovigilance - Including the EMA/PRAC deliberations and Brexit implications Vigilance 6-10
Filing eCTD Submissions Regulatory Affairs 21 17
GCP and Clinical Research Update - Hot Inspection Topics Clinical Research 3 24
MBA Strategic Thinking for Pharma and Biopharma Professionals Leadership & Strategy 25-26
Managing Vendor/CRO/CMO Oversight Clinical Research 10-11 19-20
Metrics and Earned Value in Clinical Research Projects Clinical Research 27
Navigating China’s API Regulations: An Essential Guide to DMF Registration GxP 1 1
New EU GMP Annex 1 and its Impact on Pharmaceutical Manufacturers GxP 8
Pharmaceutical Development of ATMPs GxP 20-21 16-17
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 21-24
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 14-16 11-13
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 4-5 12-13
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 26-29 5-6
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 19-20 11-14
Pharmacovigilance Vigilance 11-13
Pharmacovigilance Aspects of Licensing Agreements Vigilance 20 29-30
Pharmacovigilance QMS & Inspection Preparation Vigilance 28-29
Pharmacovigilance for Drug Safety, Regulatory Affairs and PV Auditors - Broadening your Knowledge Vigilance 2-4
Positive Persuading and Influencing Skills for Pharma Professionals Management 5-6 13-14
Practical Requirements of the Arab Pharmacovigilance Guidelines Vigilance 19-20
Process Validation with Qualification GxP 27-28
Project Management for Pharma Professionals Project Management 19-20 28-29 4-5
Regulatory Affairs for Support Staff Regulatory Affairs 26-29
Regulatory Strategies for Orphan Drugs Regulatory Affairs 26 27
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 13
Root Cause Analysis (RCA) and Critical Thinking Management 25 6
Signal Detection and Regulatory Expectations Vigilance 3-4 14-17
Smart Packaging and Electronic Patient Information GxP 12 6-7
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 13-14 13-14
Successful Medical Writing Medical Writing 2-4 6-8
The Common Technical Document GxP 10-11 27-28
The FDA Drug Approval Process Regulatory Affairs 14-15 2-3
The Leadership and Management Summer School for Pharma Professionals Leadership & Strategy 31-4
The Pharma Mini MBA Leadership & Strategy 2-4 8-10
US FDA - Understanding Key Factors When Working with the FDA Regulatory Affairs 20
Understanding Active Pharmaceutical Ingredients (APIs) - A Comprehensive and Practical Introduction GxP 19-20 20-21
Understanding Computer System Validation (CSV) - A Comprehensive and Practical Introduction GxP 26-27 27-28
Understanding Pharmacovigilance Regulations in APAC Vigilance 10-11 10-11 23-24 23-24
Update - Latest Position on the New UK Clinical Trial Proposals Clinical Research 26
Variations to Marketing Authorisations Regulatory Affairs 12-13
Working with Emotional Intelligence in the Pharmaceutical and Biopharma Industry Leadership & Strategy 16