Post Marketing Surveillance
Post advertising concentrates are required or concurred by a support that are led after FDA has endorsed an item to market. FDA utilizes present advertising study duties on accumulate extra data about an item's wellbeing, adequacy, or ideal utilize. Concurrences with supporters to lead post promoting studies can be come to either before or after FDA has conceded endorsement to a support to showcase an item.
Related Conference of Post Marketing Surveillance
Post Marketing Surveillance Conference Speakers
Recommended Sessions
- Bioinformatics in Clinical Research
- Clinical and Medical Case Reports
- Clinical Data Management
- Clinical Research On Different Diseases
- Clinical Trial Site Management
- Clinical Trials and Clinical Research Conducts
- CRO (Contract Research Organization) Clinical Trials
- Drug Discovery and Development
- Entrepreneurs Investment Meet
- Ethics in Clinical Trials and Research
- Globalization of Clinical Trials and Clinical Research
- In Silico Clinical Trials
- Innovations in Clinical Trials and Research
- Nanotechnology in Clinical Trials and Research
- Outsourcing and Collaborative Research in Clinical Trials
- Patient Centric Clinical Trials
- Pharmacoepidemiology
- Pharmacogenomics
- Pharmacovigilance and Drug Safety
- Post Marketing Surveillance
- Risk assessment and management in clinical trials (QRM)