Latin America Summit on Pharmaceutical & Medical Device Regulatory Compliance
Monday, March 11 to Wednesday, March 13, 2013
The Westin Playa Bonita, Panama City
For nearly twenty years, American Conference Institute (ACI) has provided the business, legal and policy intelligence that senior decision-makers need to respond to challenges here in the U.S. and around the world. Staffed by attorneys, industry specialists, and other professionals, ACI operates as a ‘think tank’, monitoring trends and developments in all major industry sectors.
Headquartered in New York City, ACI – together with its affiliates, The Canadian Institute (Toronto) and C5 (London) – offers over 500 conferences, forums, and summits each year around the globe. Over 25,000 senior business and public sector executives, lawyers and other professionals from the United States, Canada, Europe, Russia and CIS, China, Australia, Asia, Latin America and Africa will attend our events this year.
ACI is pleased to announce its Latin America Summit on Pharmaceutical & Medical Device Regulatory Compliance, taking place March 11 – 13, 2013 in Panama City, Panama.
The Latin America Summit on Pharmaceutical & Medical Device Regulatory Compliance will be the premier program for pharmaceutical, biotech, and medical device manufacturers on reducing liability exposures when structuring and conducting clinical trials overseas. It will cover the complete international regulatory landscape, including privacy considerations, mitigating FCPA violations, interacting with the FDA and international governments, and ensuring that marketing activities are done compliantly.
Featuring multiple networking and benchmarking opportunities, your registration fee includes multiple breakfasts and lunches. Hear how your industry peers are facing the challenges unique to the Latin American region, and leave the conference with real takeaways on how to improve your research and compliance protocols.
Topics of discussion will include:
Increase your conference learning by attending the pre-conference Primer on FDA Fundamentals. Aimed at providing a primer to professionals who have limited experience working with FDA on regulatory matters, or who are new to the pharmaceutical regulatory space, this workshop will provide you with a basic overview of FDA regulations and will prepare you for the more in-depth discussions that will take place throughout the conference.
ACI looks forward to welcoming you to Panama in March. Register now by calling 1-888-224-2480 from within the U.S. or 416-926-82000 from outside the U.S. You can also register online here.
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Mon, Mar 11, 2013
Wed, Mar 13, 2013
The Westin Playa Bonita
Accreditation will be sought in those jurisdictions requested by the registrants which have continuing education requirements. This course is identified as nontransitional for the purposes of CLE accreditation.
ACI certifies that the activity has been approved for CLE credit by the New York State Continuing Legal Education Board in the amount of 13.5 hours. An additional 2.0 credit hours will apply to workshop participation, including 1.0 credit of ethics.
ACI certifies that this activity has been approved for CLE credit by the State Bar of California in the amount of 11.25 hours. An additional 2.0 credit hours will apply to workshop participation, including 1.0 credit of ethics.You are required to bring your state bar number to complete the appropriate state forms during the conference. CLE credits are processed in 4-8 weeks after a conference is held.
ACI has a dedicated team which processes requests for state approval. Please note that event accreditation varies by state and ACI will make every effort to process your request.Questions about CLE credits for your state? Visit our online CLE Help Center at www.americanconference.com/CLE