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There is a growing fear of potential fines and public relations nightmares due to the increasing demands of regulatory organizations (FDA and EMA) regarding post-market pharmacovigilance. Organizations struggle with trying to meet the increasing demands of both sets of regulations with their existing resources. Companies have had to restructure, create entirely new databases, adjust their departments, allocate funds, and increase employees’ workloads. In fact, many companies are struggling on how to approach these regulations successfully especially when it comes to the EMA laws.

Delegates at the marcus evans 3rd Pharmacovigilance, Risk Management, & Adverse Event Reporting Conference will learn and discuss how leaders in the industry are addressing challenges regarding global pharmacovigilance and benefit risk analysis. Hot topics will include the impact of the new EMA pharmacovigilance regulations, AER, signal detection, and benefit risk management. Delegates will have the unique opportunity to meet with their contemporaries to discuss the future of drug safety in post marketing.

Attending this premier marcus evans conference will enable you to:

  • · Address global pharmacovigilance regulations and updates to ensure compliance
  • · Determine best practices for data capture and data mining procedures
  • · Monitor adverse event reports to eliminate and minimize negligence
  • · Implement  new tactics to produce effective risk evaluation and mitigation strategies
  • · Execute internal and external excellence in modern pharmacovigilance

Industry leaders attending this conference will benefit from a dynamic presentation format consisting of workshops, panel discussions, and case studies. Attendees will experience highly interactive conference sessions, 10-15 minutes of Q&A time after each presentation, 4+ hours of networking, and exclusive online access to materials post-event.

Hear what previous attendees from our Pharmacovigilance Conference Series have to say:

“Great in-depth coverage of hot topics in an intimate setting that lent itself to excellent discussions.” –Novartis

“One of the best meetings I’ve attended. Excellent organization, topics, and speakers. Overall well done.” –Sanofi-Aventis

“Relevant and useful topics from industry perspective.” - Abbott

If the 3rd Pharmacovigilance, Risk Management & Adverse Event Reporting is important to your business, act now and make the appropriate connections. See the contact information below.

All information in Events In America is deemed to be accurate at the time we add it, and we take steps to verify all details and update our records when new information is provided, but as people, events and circumstances change, we caution users to independently confirm all information. and Events In America LLC make no guarantee of accuracy and assume no liability for inaccurate information.

Conference/Event Dates: 05/20/2013 - 05/22/2013
Classification: B2B
Primary Industry: Pharmaceutical
Other Industries: Pharmaceutical, Professional Healthcare
Audience: Contact Kara Drapala for the estimated attendance and the audience description.
Venue: Venue TBD
Conference Hotel URL:official hotel URL
Show Owner:marcus evans
Show Manager:Kara Drapala

Booth Size Booth Cost   Available Amenities
Call for information.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: Call
Other Booth Sizes Available: n/a

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