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Regulatory Affairs, Biotech & Pharma

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

Events

Showing 3 of 3 events

Global Pharmaceutical Regulatory Affairs Summit

21 - 23 April 2020, Berlin, Germany

THANK YOU TO EVERYONE WHO ATTENDED THE 2019 GLOBAL PHARMACEUTICAL REGULATORY AFFAIRS SUMMIT!

EU Pharmaceutical Law Forum

12 - 14 May 2020, Brussels

Europe’s Leading Pharmaceutical Law Networking and Knowledge Hub

FDA/CMS Summit

December 3-4, 2019, Washington, D.C.

IMMERSE YOURSELF IN THE LATEST US REGULATORY POLICY AT THIS CRITICAL TIME IN SCIENTIFIC INNOVATION

Training

Showing 4 of 23 coursesView all courses

Fundamentals Of EU Regulatory Affairs

Starting 3 Feb 2020, 4 weeks online

Gain a comprehensive understanding of the EU regulatory framework and explore strategies for dossier application to ensure speedy approvals

Preparing the Quality Module of the CTD

Starting 3 Feb 2020, 5 weeks online

Learn to analyse, prepare and construct the intricate details of Module 3 of your dossier to ensure a more efficient submission process

Introduction to EU Regulatory Affairs

3 - 5 Mar 2020, London

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

eCTD Submissions

19 - 20 Oct 2020, London

Discover practical solutions for managing global regulatory requirements and new challenge

Articles & Video

Showing 8 of 8 articles & video
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ESubmissions

Regulatory development opportunities for global harmonisation of eSubmissions

What's delaying the global harmonisation of eSubmissions for market authorisation? This whitepaper examines the latest developments and ongoing challenges.

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Esubmissions

Global Pharmaceutical Regulatory Affairs: Tell us your view

What challenges are affecting your regulatory strategy? Tell us your view to win a 2-day conference pass.

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Global Pharmaceutical Regulatory Affairs State of the Industry Report 2019

In early 2019, we surveyed the perspectives of pharmaceutical regulatory professionals around the world. This report reveals insights into the industry's greatest challenges.

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Regulations

China's changing pharmaceutical regulatory approval landscape

China has recently taken unprecedented steps to improve its healthcare and regulatory system. This whitepaper examines the recent changes and what opportunities and challenges they bring.

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Peptides and Oligonucleotides

Regulatory challenges and strategies for oligonucleotide, peptide and mRNA therapeutics - WHITEPAPER

Innovation

Digital Health: Advancing innovation through technology and strategic partnerships 

Commercialization

The regulatory hurdles to microbiome therapeutic commercial success

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Microbiome

The Regulatory Environment of Microbiome-Based Therapies in the US and EU - WHITEPAPER

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
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  • High-impact branding and messaging
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