Post Marketing Surveillance
Post marketing surveillance is an important component of the science of pharmacovigilance, which entails monitoring the safety of pharmaceutical goods and medical devices after they are introduced to the market. Because clinical trials—involving relatively few individuals who typically do not have additional medical conditions that exist in the general population—are the foundation for the acceptance and approval of drugs and medical devices, post-marketing surveillance can further hone, or confirm, the safety of a drug or device after it has been used in the general population by numerous individuals with a variety of medical conditions.
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Post Marketing Surveillance Conference Speakers
Recommended Sessions
- Bioinformatics-Based Clinical Research
- Clinical data management
- Clinical research and clinical trials: an academic perspective
- Clinical research in oncology
- Clinical research on stem cells and genetics
- Clinical studies on various disorders
- Clinical study design advancements
- Clinical trials conduct
- Drug research and development
- Ethics in clinical research
- Future & innovations of clinical trials
- Globalization of clinical trials
- Medical and clinical case reports
- Patient-Centric clinical trials
- Pharmacoepidemiology
- Pharmacogenomics
- Pharmacovigilance & drug safety
- Post Marketing Surveillance
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