Choosing the most suitable physician as medical reviewer for safety monitoring is always an important part of any company’s pharmacovigilance responsibilities. Yet, it is important to keep in mind that the qualities and expertise that this key safety team member will be called upon to provide will differ depending on the particular safety scenario the company is facing. Knowing what is required and expected of the safety medical reviewer in these differing circumstances, and what factors determine the best choice, is integral to the overall smooth performance of the safety team.
Contact the event managers listed below for more information about how you can participate at the The Differences Between Clinical and Post Market Medical Reviews.
|Conference/Event Dates:||03/30/2016 - 03/30/2016|
|Primary Industry:||Clinical Pharmacology|
|Other Industries:||Business, Clinical Pharmacology, Professional Healthcare, Safety|
|Audience:||Senior level professionals working on the development of regulated health products such as drugs, RX, OTC, animal health, vaccines, medical devices, or products.
Job functions also include:
Heads of Medical Affairs
Pharmacovigilance Medical Directors
Regulatory Affairs Professionals
Chief Science, Safety or Medical Officers
For pharmaceutical, biotech, cosmetic, and medical device companies
|Booth Size||Booth Cost||Available Amenities|
|Marketing Vehicles Allowed:||n/a|
|Other Booth Sizes Available: n/a|
How do I show up here?
Add a note here, it is only visible by you.