'Regulatory experience' presentation slideshows

Presentation By Prayas Energy Group, India prayaspune/peg

421 views • 23 slides

Inmarsat - Products and Strategy

Inmarsat - Products and Strategy. Workshop on Satellite in IP and Multimedia Gene Jilg, Chief Technology Officer. Overview of Inmarsat Today. Leading global mobile satellite communications service provider Data and voice to maritime, land and aeronautical users

486 views • 17 slides

Genetic Engineering Drug Development with Regulation Policy and Humans and the Environment and Ethical Issues

Genetic Engineering Drug Development with Regulation Policy and Humans and the Environment and Ethical Issues. Cai Wu. (4/24/2006). Outline. Introduction Biotechnology and Drug Development Genetic engineering Pharmaceuticals Biotechnology Industry Facts Government Regulations

2.2k views • 16 slides

Economic Society of Australia Business Symposium University of Sydney 30 September 2004

Economic Society of Australia Business Symposium University of Sydney 30 September 2004. Infrastructure Investment in Australia - Is there an Emerging Crisis? Implications for Economic Regulation of Future Infrastructure Investment. John Tamblyn Chairperson

444 views • 13 slides

RAC US Braindumps

Regulatory Affairs Specialist is one of the best certifications in the field of Drugs and medical. Most of the students choose this for the better career in the medical field. Dumpsbook provides you RAC US Exam Questions along with RAC US Test Engine. They have best quality RAC US Exam Dumps, So you can easily prepare and pass the exam on the first attempt. Visit us today and get a special discount on RAC US Braindumps by using this coupon code. "OFF20". https://www.dumpsbook.com/Exam/RAC-US

113 views • 10 slides

U.S. Cosmetic Regulations and New Legislation

This webinar will cover laws and regulations for successful marketing and compliance of cosmetics in the U.S. It will help clarify what claims and product labeling are appropriate for cosmetics to market them successfully and avoid regulatory issues and problems with FDA compliance and competitive challenges. Current FDA Warning letters to cosmetic firms will be reviewed. Adverse Event Reporting requirements for cosmetics will be discussed with focus on how these requirements will change under newly proposed legislation for cosmetics: The Personal Care Products Safety Act.

141 views • 5 slides

SAPA-GP Webinar Program A Professional Training Tool for SAPA Members Non-members are Welcome to Participate

SAPA-GP Webinar Program A Professional Training Tool for SAPA Members Non-members are Welcome to Participate. January, 2013 Introduction of Early Drug Development Dr. Sean Zhang , MD, FCP Medical Director, Bristol-Myers Squibb (BMS) February, 2013

196 views • 4 slides