This webinar will present regulatory compliance considerations and regional differences for regulated and/or registered products for the U.S., Canada, the EU, Latin America and countries in the Asia / Pacific rim, to make the expansion to that region a success.
Why Should You Attend:
Many companies across Consumer Products, Food, Cosmetic and Life Science offerings are expanding sales by taking their products global. It is much more cost effective in expanding on registrations and licenses already in place in one part of the World, than in developing new products for a specific region. Being ready in knowing what to expect, what resources must be in-place, what supportive data will be required and how language and cultural norms factor into your country success rate can be underestimated or simply overlooked.
This live & interactive webinar will present considerations and regional differences for the U.S., Canada, the EU, Latin America and many countries in the Asia / Pacific rim. We will discuss what you will encounter as a regulated and / or registered product as we march around the globe. Leaving this seminar, you should walk away with a sequencing of considerations, that must be nailed down, to consider the expansion to that region a success. Realistic timing of events will be discussed in order to accurately set internal timeline expectations.
At the conclusion of presentation, we will open the lines for specific Q&A with the speaker. Companies previously attending this discussion have said it opened up their minds to thinking very differently as they globally expanded.
Areas Covered in the Webinar:
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies, with products requiring notification or registration within a country before importation will be allowed. The employees who will benefit include:
Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment
Recorded video session
Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bob has more than 25 years of experience working with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process. Prior to entering the consulting field, Mr. Russell was the Global Director of Regulatory Affairs for two Fortune 100 firms. These companies were major raw material suppliers to the pharmaceutical and medical device industry and one a joint-venture parent of a major pharmaceutical division.