Conference Details

4th Adverse Event Reporting and Safety Strategies Summit Adverse events are the pillars of pharmacovigilance and safety operations as we know them. They are the drivers for developing safety databases, risk management plans, risk evaluation and mitigation strategies, benefit-risk assessments, and periodic reports. Their collection and reporting is instrumental in leading to preventative actions for marketing better and safer drugs.

Date :

Place : United States, Philadelphia

Website :

Contact Person:Paula Edwards

Description:

4th Adverse Event Reporting and Safety Strategies Summit Adverse events are the pillars of pharmacovigilance and safety operations as we know them. They are the drivers for developing safety databases, risk management plans, risk evaluation and mitigation strategies, benefit-risk assessments, and periodic reports. Their collection and reporting is instrumental in leading to preventative actions for marketing better and safer drugs.

4th Adverse Event Reporting and Safety Strategies Summit Adverse events are the pillars of pharmacovigilance and safety operations as we know them. They are the drivers for developing safety databases, risk management plans, risk evaluation and mitigation strategies, benefit-risk assessments, and periodic reports. Their collection and reporting is instrumental in leading to preventative actions for marketing better and safer drugs. will be held in Philadelphia,United States on date 2017-12-05

Deadline for abstracts/proposals : 1st December 2017

Organized By :New York Events List

Keynote Speakers :

Conference Highlights :This conference is designed for professionals from pharmaceutical, biotech and medical device companies with responsibilities in the following areas: Pharmacovigilance Drug Safety Risk Management Safety Research/Epidemiology Pharmacoepidemiology Medical Product Safety Assessment Regulatory Affairs Clinical Research

Venue :Philadelphia, PA 19103, United States

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4th Adverse Event Reporting and Safety Strategies Summit
Adverse events are the pillars of pharmacovigilance and safety operations as we know them. They are the drivers for developing safety databases, risk management plans, risk evaluation and mitigation strategies, benefit-risk assessments, and periodic reports. Their collection and reporting is instrumental in leading to preventative actions for marketing better and safer drugs.

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