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Regulatory Affairs, Biotech & Pharma

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

Events

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EU Pharmaceutical Law Forum

16 - 20 November 2020, Delivered in Central European Time (CET)

Europe’s Leading Pharmaceutical Law Knowledge & Networking Hub

European Pharma Law Academy

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 25 coursesView all courses

EU & US Requirements for Pharmaceutical Labelling & Package Leaflets

9-19 November 2020, 8 sessions delivered over 2 weeks

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

Filing Variations

TBC in 2021, 6 sessions delivered over 2 weeks

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

Regulatory Guide to the Generics Market

23 November 2020, 3 weeks

Develop your understanding of EU and US regulations for generics to ensure swift approvals and maximise generic market share potential

Project Management For Regulatory Affairs Professionals

1-12 December 2020, 6 sessions delivered over 2 weeks

Learn to apply project management techniques to streamline your regulatory procedures

Articles & Video

Showing 9 of 37 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.

MedTech eBook Series

Clinical Evaluations for Medical Devices and IVDs - MedTech eBook Series

Discover how the EU MDR will affect clinical evaluations for medical devices and IVDs in this MedTech Summit eBook.

COVID-19

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

Regulatory affairs

What is standing in the way of global harmonisation?

Healthcare

REPORT: The Future of Healthcare Post COVID-19

Diversity and Inclusion

Women in Pharma: 44% of pharma professionals think that women are under represented in their organization

ANVISA

Regulations in Brazil: What the drug approval process is like in 2020

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

All opportunities can be customised to align with your needs and budget. Examples may include:

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