Global Events - Discuss Critical Issues with Pharma Industry Experts

Discuss Critical Issues with Industry Experts Want to network and exchange knowledge with regulatory agencies from around the world? Then don’t miss the Latin American Regulatory Conference (LARC) 2013. High-profile regulatory agencies will be participating in the meeting, to be held in Bogota, Colombia from May 15-16, to discuss the current regulatory landscape and its impact on future research and drug development. Representatives will be attending from Colombia (INVIMA), Ecuador (MoH), Guatemala (MoH), Chile (ISPCH), Brazil (ANVISA), the USA and Costa Rica (FDA), Canada (Health Canada), Spain (AEMPS), and Peru (DIGEMID). Global organizations including the Pan American Health Organization and the World Health Organization will also be taking part. Find out More Download Program Register now CALL FOR ABSTRACTS worldwide Don’t miss great opportunities to share knowledge with professionals around the globe. Click to Submit In Other News NEW MEMBER BENEFIT FREE Archived Webinars! OTHER EVENTS 6th Regulatory Conference in IndiaMay 23-24, 2013 Ahmedabad, India Asia New Drug Development April 15-16, 2013 Tokyo, Japan DIA/FDA Statistics Forum 2013: PDUFA V Statistical Topics and Emerging New Issues April 28-May 1 North Bethesda, MD Busy professionals need affordable, convenient access to the latest updates in the life sciences industry. That’s why DIA developed comprehensive online training courses and webinars designed for our global audience. Online Training Course: How to Prepare for a Safety Inspection March 26-28 | 11:00AM-1:00PM ET Register by March 22 to Save $100! Enter promo code SAFE at checkout Webinar: CDER – Data Submission 101 March 27 | 10:00-11:30AM ET Online Training Course: Fundamentals of Project Management for the Nonproject ManagersApril 9, 11, 16 & 18 | 12:00-1:30PM ET Online Training Course: Strategies for Comparative Effectiveness Research for Regulatory, Compliance and Legal Professionals in Life Sciences Promotion April 23 | 11:00AM-12:30PM ET Register for multiple courses in this CER series and save up to 20%! Two-Part Webinar Series: Impact of the New European Pharmacovigilance Legislation and Important Updates April 25-26 | 10:00-11:30AM ET Webinar: A Closer Look at FDASIA Provisions to Promote Biomedical Innovation April 29 | 1:00-2:30PM ET Book by April 22 for Early-bird Savings Register for the 5th DIA China Annual Meeting before April 22 to save with our early-bird discount. The conference, to be held in Beijing from May 12-15, will feature more than 40 sessions and 14+ tracks on hot topics from key opinion leaders in the global pharmaceutical industry, government agencies, and life sciences organizations. Global expansion, regulatory affairs, clinical research, pharmacovigiliance, and traditional Chinese medicines will be discussed in presentations and sessions at the event, focused this year on “Patient Safety – A Sustained Focus from Scientific Ideas to Innovative Medicines.” Read More Register

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Join high-profile global regulators, industry professionals, and academia to discuss current regulatory landscape in Latin America

Plan your Attendance at LARC 2013 Take a look at this overview of the insightful sessions coming to the Latin American Regulatory Conference (LARC) 2013. Not registered yet? Book your seat before April 12 to save with an early-bird discount! Join high-profile global regulators, industry professionals, and academia to discuss the current regulatory landscape and its impact on future research and drug development at the event in Bogota, Colombia from May 15-16. Find Out More Download the Program Register 2012 VIDEO HIGHLIGHTS Watch videos from last year’s Latin American conferences and get a taste of what you can expect from these insightful events in 2013. IT ONLY TAKES A FEW MINUTES... Update your customer profile to ensure that you receive communications tailored to your specific area(s) of interest. Session Highlights Updates on Regional and Global Convergence with perspectives from Chile, Colombia, Canada, the PAHO and WHO Latin American Agencies Profiles by CIRS: Number of Reviewers, Inspectors, Timeliness, Predictability and Quality of a Full Review Case Study: Challenges faced by Regulators in the Adoption of Internationally Recognized Technical Guidance Documents and Standards Risk Based Approach to Inspections Integrity of the Supply Chain: Serialization, Counterfeits and Disposal of Expired Drugs Transparency of Review Process Health Technology Assessment Implementation of e-Submissions “Miracle” Drugs and Pharmaceutical Products Bordering Dietary Supplement Find Out More Download the Program Register

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Highlights for upcoming Latin American Regulatory Conference - May 15-16, Bogota

Check out the Highlights for LARC 2013 Download the program and see what’s in store at the Latin American Regulatory Conference (LARC) 2013. Join global regulators, industry professionals and academia to discuss the current regulatory landscape and its impact on future research and drug development at the event in Bogota, Colombia from May 15-16. The LARC 2013 will focus on “Pharma-Co-Vergence” – the act of achieving pharmaceutical regulatory convergence through stakeholders’ collaboration – highlighting the true collaborative spirit of this multidisciplinary global conference. Attendees will learn how to define the various initiatives related to global regulatory environment and their impact on the access of medicines and future R&D in Latin America, and discuss the progress of the Pan American Network for Drug Regulatory Harmonization (PANDRH) convergence process and working groups. Download the Program Read More Register 2012 VIDEO HIGHLIGHTS Watch videos from last year’s Latin American conferences and get a taste of what you can expect from these insightful events in 2013. IT ONLY TAKES A FEW MINUTES... Update your customer profile to ensure that you receive communications tailored to your specific area(s) of interest. Featured Topics Regulatory Landscape and Convergence Initiatives Strengthening the Regulatory Framework Efforts Underway by Convergence Initiatives Reviews and Inspections Ethics Committee Research in the Regions Post-market Research Studies and Better Medicines to Influence Efficacy and Effectiveness Perspectives and Regulations of Pediatric Studies Drug Safety, Marketing Surveillance and Quality Control Monitoring Regulatory Concerns: Health Systems and Security of the Supply Chain Current Regulations of Biologics and Biosimilars Emerging Topics Who Should Attend Professionals involved in: Regulatory affairs Clinical research and development Clinical safety and pharmacovigilance Clinical trial and project management Drug development and discovery Medical and scientific affairs Preclinical development Quality assurance Research and development Strategic sourcing/planning Download the Program Read More Register

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