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Regulatory Affairs, Biotech & Pharma

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

Events

Showing 4 of 5 eventsView all events

Global Pharmaceutical Regulatory Affairs Summit

20th - 22nd April 2021

IDMP, eSubmissions, Global Regulations: Critical Updates Directly to Your Screen

European Pharma Law Academy

September 2021, Cambridge University

European Pharma Law Academy

EU Pharmaceutical Law Forum

2021 Dates Coming Soon!

Europe’s Leading Pharmaceutical Law Knowledge & Networking Hub

Advanced Regulatory Strategies for Veterinary Drug Development

24-25 June 2020, London

Advanced Regulatory Strategies for Veterinary Drug Development

Training

Showing 4 of 25 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

Fundamentals Of EU Regulatory Affairs

TBC, 4 weeks

Gain a comprehensive understanding of the EU regulatory framework for drug development and dossier submission

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

TBC, 6 sessions delivered over 2 weeks

Learn to apply project management techniques to streamline your regulatory procedures

Articles & Video

Showing 9 of 38 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.

Regulatory Information Management

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

Many companies are putting themselves at risk lacking AI -powered RIM systems for regulatory data management. Get the details in this complimentary article.

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?

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

SPONSORSHIP & EXHIBITION OPPORTUNITIES

Let us help you engage qualified decision makers in need of experts and services to navigate global life science regulation. Share your strategy and plans so we can help you identify the best opportunities to reach your objectives. Our team will collaborate with you to develop a bespoke program tailored to your unique needs.

To find out more about sponsor opportunities, contact Linda Cole:
linda.cole@informa.com | +44 207 017 6631

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

  • Exhibition space
  • Speaking slots and onsite video interviews
  • High-impact branding and messaging
  • Private/public hosted events (lunches, breakfasts, and receptions)
  • Custom digital campaigns
DOWNLOAD SPONSOR PROSPECTUS

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