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Regulatory Affairs, Biotech & Pharma

Where regulatory meets e-regulatory: bringing answers to the pharmaceutical industry.

Events

Showing 5 of 5 events
Featured

Global Pharmaceutical Regulatory Affairs Summit

20th - 22nd April 2021, Presented in Central European Time (CET)

Thank you for joining us in 2021! Check back soon for more information on the 2022 event.

Featured

EU Pharmaceutical Law Forum

17th - 20th May 2021, Delivered in Central European Time (CET)

The Go To EU Pharmaceutical Law Conference for In-House and External Lawyers Alike

European Pharma Law Academy

6-10 September 2021, Cambridge University

European Pharma Law Academy

Advanced Regulatory Strategies for Veterinary Drug Development

24-25 June 2020, London

Advanced Regulatory Strategies for Veterinary Drug Development

Global Pharmaceutical Regulatory Affairs Summit Digital Week

24th - 25th June 2020, Digital Week

Discover the latest insights into RIM, SPOR, IDMP from task force members and industry experts with this complimentary 2-day webcast series

Training

Showing 4 of 19 coursesView all courses

Filing Variations

17-18 June 2021, 2 sessions over 2 days

Ensure speedy regulatory approval and guarantee your filing variation procedures are cost-effective

EU & US Requirements for Pharmaceutical Labelling & Package Leaflets

23-25 June 2021, 3 sessions over 3 days

Further your understanding of the latest requirements for labelling and packaging according to EU and FDA guidelines

Gaining Marketing Authorisations In CIS For Pharmaceuticals And Biotech

TBC, 5 sessions delivered over 2 weeks

An essential overview of regulatory requirements to ensure successful strategies for gaining market access in the CIS

Introduction to EU Regulatory Affairs

21-23 April 2021, 3 sessions over 3 days

Gain a strategic insight into the EU regulatory framework and learn how to improve your dossier compilation process

Articles & Video

Showing 9 of 40 articles & videoView all articles & video
Premium
Regulatory affairs

Pharma and Medical Device Regulations Content Library: Whitepapers and Reports Collection

Explore our collection of exclusive whitepapers and reports covering the hottest topics in pharma, biotech and medical device regulatory affairs and law with one simple registration.

Featured

The Future of the Global Pharmaceutical Regulatory Affairs Industry

In a new interactive ebook, we take a deep dive into the challenges and trends we may see in pharmaceutical regulatory affairs over the next decade.

Regulatory affairs

Post-event Report: Global Pharmaceutical Regulatory Affairs Summit 2020

This report takes a detailed look back at the 2020 virtual Global Pharmaceutical Regulatory Affairs Summit.

Diversity and Inclusion

REPORT: Diversity, Equity and Inclusion in the Life Sciences 2021

Explore the Diversity, Equity and Inclusion in the Life Sciences 2021 report based on an exclusive study of 483 industry professionals.

Diversity and Inclusion

SURVEY: Diversity, Equity and Inclusion in the Life Sciences 2021

Regulatory Information Management

Is your Regulatory Information Management process putting your company at risk?

MedTech eBook Series

Clinical Evaluations for Medical Devices and IVDs - MedTech eBook Series

COVID-19

Report: Partnering And Deal-Making in Pharma through the Pandemic

Regulatory affairs

What is standing in the way of global harmonisation?

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linda.cole@informa.com | +44 207 017 6631

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