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Compiling Successful Clinical Trial Applications

Location London, UK

Cost of Event £1,095*

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Regulatory Affairs Senior Associate / Associate Manager - CTA

Location North London,

Salary £40,000 - £52,000

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Global Regulatory Strategy for Pharmaceuticals

Location At your desk,

Cost of Event $455*

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Regulatory Global Labelling Lead

Location Home Based,

Salary £60,000 - £70,000

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Electrical, Electronic and Software Medical Devices

Location London, UK

Cost of Event £675*

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Medical Devices: EU Regulations

Location At your desk,

Cost of Event $535*

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A Practical Guide to Writing Risk Management Plans (RMPS)

Location London, United Kingdom

Cost of Event £699*

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Intermediate Course for Regulatory Submissions in eCTD Format

Location San Diego, California, USA

Cost of Event $1,450*

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Pharmaceutical Regulatory Affairs in the EU and US

Location At your desk,

Cost of Event £999*

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Senior Regulatory Affairs Officer - Labelling – Global

Location Greater London - commutable from Edgware, Uxbridge, St Albans, Slough & Enfield areas,

Salary £42,000 - £50,000

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Essentials and Overview of the Regulatory Framework in Europe

Location Nanterre, France

Cost of Event €1605*

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Introduction to Electronic Regulatory Submissions in the eCTD Format

Location San Diego, California, USA

Cost of Event $1,450*

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Regulatory Director / Associate Director – (ATMP)

Location London or Cambridge ,

Salary Competitive

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Introduction To Medical Device Regulation in Europe

Location Chesham, Buckinghamshire, UK

Cost of Event £1,700*

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Regulatory Affairs Manager - EU

Location Central London,

Salary £50 - £55,000

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Getting the CMC Dossier Right

Location London, UK

Cost of Event £1095*

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Regulatory Convergence

Location Vancouver, BC, Canada

Cost of Event

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Medical Devices Symposium

Location Stockholm, Sweden

Cost of Event £525*

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Project Management for Regulatory Affairs Professionals

Location London, UK

Cost of Event £TBA

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An Introduction to Risk Evaluation & Mitigation Strategies (REMS)

Location London, UK

Cost of Event £699*

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Essentials of European Medical Device Regulatory Affairs

Location Ireland

Cost of Event £360

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Regulatory Strategy for Established Active Substances - Masterclass

Location Chesham, Buckinghamshire, UK

Cost of Event £1,700*

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Managing Variations Effectively

Location London, UK

Cost of Event £675*

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Regulatory Affairs Manager

Location Hertfordshire,

Salary £40,000 - £55,000

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Clinical Trial Regulatory Requirements

Location London, United Kingdom

Cost of Event £1,299 *

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A Practical Guide to Producing and Maintaining the PSMF

Location London, United Kingdom

Cost of Event £699*

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Regulatory Procedures for New Drug Applications / Biologics License Applications in the US

Location London, United Kingdom

Cost of Event €1395*

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Human Medicines Symposium

Location Stockholm, Sweden

Cost of Event £2,195*

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Intermediate Course for Regulatory Submissions in eCTD Format

Location Rockville, Maryland, USA

Cost of Event $1,550*

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Introduction to Electronic Regulatory Submissions in the eCTD Format

Location Rockville, Maryland, USA

Cost of Event $1,450*

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Essentials of European Pharmaceutical Regulatory Affairs

Location London, United Kingdom

Cost of Event £580

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Quality Assurance & Regulatory Affairs Officer - Pharmaceuticals

Location Slough,

Salary £55,000 - £60,000

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Writing Effective Product Information

Location London, UK

Cost of Event £810*

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Regulatory Affairs Manager - Emerging Markets - 4 positions available

Location Central London,

Salary Competitive

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Essentials of European Pharmaceutical Regulatory Affairs

Location London, United Kingdom

Cost of Event £580

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Regulatory Aspects in Pharmacovigilance and Practical Examples

Location London, United Kingdom

Cost of Event €1605*

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Regulatory Affairs Senior Officer

Location South London, England

Salary £40,000 - £50,000

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Understanding Clinical Development

Location London, UK

Cost of Event £1,095*

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Brexit - What does it mean for the Life Sciences

Location London, UK

Cost of Event £595*

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Global Regulatory Strategy & Drug Development in Asia, Latin America, & Other Emerging Markets

Location Nanterre, France

Cost of Event €1605*

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EU Health Authorities Scientific and Regulatory Advice

Location Nanterre, France

Cost of Event €955*

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Search our jobs and training sections

Let us help you advance your career

Compiling Successful Clinical Trial Applications

Regulatory Affairs Senior Associate / Associate Manager - CTA

Global Regulatory Strategy for Pharmaceuticals

Regulatory Global Labelling Lead

Electrical, Electronic and Software Medical Devices

Medical Devices: EU Regulations

A Practical Guide to Writing Risk Management Plans (RMPS)

Intermediate Course for Regulatory Submissions in eCTD Format

Pharmaceutical Regulatory Affairs in the EU and US

Senior Regulatory Affairs Officer - Labelling – Global

Essentials and Overview of the Regulatory Framework in Europe

Introduction to Electronic Regulatory Submissions in the eCTD Format

Regulatory Director / Associate Director – (ATMP)

Introduction To Medical Device Regulation in Europe

Regulatory Affairs Manager - EU

Getting the CMC Dossier Right

Regulatory Convergence

Medical Devices Symposium

Project Management for Regulatory Affairs Professionals

An Introduction to Risk Evaluation & Mitigation Strategies (REMS)

Essentials of European Medical Device Regulatory Affairs

Regulatory Strategy for Established Active Substances - Masterclass

Managing Variations Effectively

Regulatory Affairs Manager

Clinical Trial Regulatory Requirements

A Practical Guide to Producing and Maintaining the PSMF

Regulatory Procedures for New Drug Applications / Biologics License Applications in the US

Human Medicines Symposium

Intermediate Course for Regulatory Submissions in eCTD Format

Introduction to Electronic Regulatory Submissions in the eCTD Format

Essentials of European Pharmaceutical Regulatory Affairs

Quality Assurance & Regulatory Affairs Officer - Pharmaceuticals

Writing Effective Product Information

Regulatory Affairs Manager - Emerging Markets - 4 positions available

Essentials of European Pharmaceutical Regulatory Affairs

Regulatory Aspects in Pharmacovigilance and Practical Examples

Regulatory Affairs Senior Officer

Understanding Clinical Development

Brexit - What does it mean for the Life Sciences

Global Regulatory Strategy & Drug Development in Asia, Latin America, & Other Emerging Markets

EU Health Authorities Scientific and Regulatory Advice

Come and join our community!

We are ready and waiting for you