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Train Your Entire Team at Global Pharmaceutical Regulatory Affairs Summit Virtual

Provide your entire team, division or company across multiple sites with access to Global Pharmaceutical Regulatory Affairs Summit Virtual by purchasing a company license, valid for anywhere between 10+ to 250+ attendees within a single company, at an affordable price per person.

Request pricing for a company license by filling out the short form at the link below.

Company License Benefits

Securing a company license to Global Pharmaceutical Regulatory Affairs Summit Virtual provides an affordable way to keep your team up to date on the latest in:

  • IDMP Updates
  • Regulatory Information Management
  • Regulatory Affairs in Latin America
  • Regulatory Affairs in Asia-Pacific
  • Regulatory Affairs in Russia, CIS, MENA & Turkey
  • Global eSubmissions
  • Telematics Policy

Book your company license today to provide each member of your team with access to the following benefits:


Expert Regulatory Guidance From Key Authority Speakers
Expert Regulatory Guidance From Key Authority Speakers

Ensure you team is up-to-date with the latest regulatory insights from government bodies, regulatory authorities, IDMP Taskforce members and experts in the pharmaceutical regulatory landscape. Your team will learn from the likes of:

  • ANVISA,
  • COFEPRIS
  •  Iraqi Ministry of Health
  • Bristol-Myers Squibb
  • DKMA, PPG Inc.
  • Merck
  • Sharp & Dohme

 and many more!

Comprehensive Coverage Across Multiple Fields Of the Regulatory Landscape
Comprehensive Coverage Across Multiple Fields Of the Regulatory Landscape

Make the most the added benefit of access to all of the conference tracks taking place on the days you choose to attend! 

Your company license passes will allow your team to attend the full conference, or jump in and out according to their preferred days and talks - allowing them to personlise their conference experience to their schedule and job demands.

With so much valuable content on offer, be sure to browse the full agenda to make sure you and you're team make most out of this comprehensive Global Pharmaceutical Regulatory Affairs Summit virtual experience.

Plus, your team will have access to the event's content for 30-days after the live dates with our on-demand* library. That's 70+ sessions with the option of on-demand access!

Take a look at the agenda at a glance below to start planning your company license package.


*Excluding sessions limited to live-viewing only. Subject to speaker permissions.

Virtual Networking With Interactive Content
Virtual Networking With Interactive Content

This year’s virtual format offers live Q&A sessions, interactive discussion panels, and dedicated networking breaks. Connecting with those who matter has never been easier! 

No need to bump into the right contact, you will have access to the full attendee list upon registration – giving you the tools to connect with peers, continue discussions with speakers and expand your network. 

You will be able to make the most of the live Q&A's, interactive round-tables and plenty more, to connect with peers, speakers and service providers - meaning you receive the full conference experience in the comfort of your own seat!

Global Pharmaceutical Regulatory Affairs Summit At A Glance


Register for the company licensing pass and your team can take advantage of obtaining complete access to all 4 conference tracks at Global Pharmaceutical Regulatory Affairs Summit 2021.