Pharmacovigilance & Drug Safety
Pharmacovigilance is characterized as the science and exercises identifying with the recognition, appraisal, comprehension and counteractive action of unfriendly impacts or some other medication-related issue. Medication wellbeing identifies with the potential for unfavorable impacts identified with the organization of medications. Endeavors to set up the secure profile of medications start right off the bat in their improvement, within vitro, and in vivo harmfulness testing, and proceed through clinical preliminaries paving the way to sedate endorsement and following endorsement in explicit post-promoting studies or general pharmacovigilance endeavors
- Clinical development programme
- Cross-sectional studies
- Company core data sheet (CCDS)
- Descriptive studies
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Pharmacovigilance & Drug Safety Conference Speakers
Recommended Sessions
- 12.Pharma Audit, GMP, GCP & Quality Control
- Adoption of Innovative Clinical Operations Technology
- Clinical & Experimental Dermatology
- Clinical and Medical Case Reports
- Clinical Data Management
- Clinical Trials on Different Diseases
- Clinical Trials Pharmacovigilance
- Design of Clinical Studies and Trials
- Diversity in Industrial Clinical Trials and Clinical Research
- Pharmacovigilance & Drug Safety
- Regulatory Affairs
- Risk assessment and management in clinical trials
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