Pharmacovigilance

Bioquest provides drug safety and risk management services to pharmaceutical, biotechnological, and medical device companies. Their expertise ensures the timely submission of high-quality adverse event data to regulatory authorities worldwide. The Bioquest Pharmacovigilance teams possess in-depth knowledge of local regulations, care standards, and cultural practices, enabling them to effectively identify and assess risks during clinical trials, there by safeguarding the safety of study subjects.

Our Drug Safety Services Includes

• Customized Safety Survelliance
• Safety Narrative Writing
• Safety Signal Management
• Aggregate Report Management
• Adverse Event & Product Compliant Management
• Individual Case Reporting
• Developmental Safety Update Report (DSUR)
• Safety Database Services
• Clinical Adjudication Committee Management
• Signal Detection and analysis
• Eudravigilance Reporting