Get the latest updates on regulatory compliance in the US, Brazil, the EU, India, Russia and more.

Learn about important recent changes in serialization rules in the US, Brazil, the EU, India and Russia. New mandates are on the horizon for many countries. Right now, sustaining product readiness and preparing for the introduction of new vaccination manufacturing lines is top of mind. Following this guidance will help you to minimize costs and ensure timely compliance to mandates.

In this 45-minute webinar, regulatory expert Dirk Rodgers will review compliance changes in the US, Brazil, the EU, India, Russia and more, including:

  • US: VRS, the FDA pilot and the DSCSA impact on the COVID-19 pandemic
  • EU FMD: Dual unique identifier/anti-tamper device mandate
  • Brasil: Anvisa timeline changes
  • India: Switch from DAVA to iVEDA Portal
  • Russia: Prescription and OTC products requirements
  • Quick updates on Indonesia, Australia, China, Saudi Arabia, Lebanon and EU (Nordic countries)

There will be an interactive live Q&A session following the briefing.

Date | August 12, 2020
Time | 11:00 NYC | 16:00 London
Duration | 45 Minutes

 

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Join "Global Pharmaceutical Regulatory Update | Summer 2020" 

Speakers

 

dirk-rodgersDirk Rodgers
Global Regulatory Strategist,
RxTrace Founder



Dirk Rodgers is a Regulatory Strategist and writes regularly in an exploration of the intersection between the pharmaceutical supply chain, track and trace technology, standards and regulatory compliance. He has posted over 600 essays on these specific topics and is the author of the book “The Drug Supply Chain Security Explained” (Amazon). A logical thinker, Dirk is skilled at making complex technical topics understandable to non-technical readers and listeners. An Electrical and Computer Engineer by education, Dirk has worked as a consultant, software architect and automation engineer during a career spanning 30 years. Dirk has served on HDA, NCPDP, EPCglobal, GS1 and GS1 US technical and standards work groups.

 

steve-tallantSteve Tallant
Senior Director, Market
Development, Systech



Steve is a brand marketing and product management expert with over 25 years of experience. He’s worked in a myriad of vertical industries with enabling technologies including anti-counterfeiting, supply chain and product lifecycle management. As a thought leader, Steve has written several white papers and is a frequent contributor of content to global industry publications across pharmaceutical and consumer packaged goods industries. His specialty areas include supply chain security, traceability, blockchain and brand/consumer protection.