Continuous Monitoring. Patient Safety. Scientific Vigilance.
Aidotick Pharmaceuticals maintains a structured pharmacovigilance (PV) framework designed to ensure the safe and responsible use of all products manufactured under our license.
Pharmacovigilance is a core component of our global commitment to patient protection.
Our PV System Ensures:
1. Early Detection of Adverse Events (AEs)
We actively monitor:
- Adverse drug reactions (ADR)
- Quality complaints
- Product-related incidents
- Unexpected therapeutic responses
2. Reporting & Documentation
All cases follow international PV documentation protocols and are reviewed by trained personnel.
3. Regulatory Communication
We collaborate with local Ministries of Health to ensure mandatory reporting is completed in a timely and transparent manner.
4. Continuous Benefit–Risk Assessment
Each product undergoes ongoing evaluation throughout its market lifecycle.
5. Partner Support
Distributors and healthcare professionals receive:
- Guidance on identifying AEs
- Support for completing AE forms
- Response to safety-related queries
How to Report an Adverse Event
If you experience or observe an adverse event, please contact:
📧 safety@aidotickpharma.com
📱 WhatsApp Hotline (optional placeholder): +91-9979015551
📝 Online PV Reporting Form (to be added on site)
All reports are handled confidentially and scientifically.