Quality you can trust, compliance you can verify
Every Saneveda medicine is made to WHO-GMP standards, marketed under valid Indian drug licences, and promoted within the bounds of India's pharmaceutical regulations. Here's how we hold that line.
WHO-GMP manufacturing
Our products are manufactured at WHO-GMP certified facilities operating under Good Manufacturing Practices as defined by Schedule M of the Drugs & Cosmetics Act.
- Controlled, validated production environments
- Batch-wise quality control and release testing
- Stability testing to support shelf-life claims
- Full traceability from raw material to finished pack
Regulatory compliance
We operate under the Drugs & Cosmetics Act, 1940 and its Rules. All our medicines are Schedule H prescription drugs, sold only against a valid prescription.
- Valid manufacturing / marketing drug licences
- Approved labelling and pack inserts
- "For the use of a registered medical practitioner only" on Rx material
- Compliant storage and distribution practices
Ethical promotion (UCPMP)
Our engagement with healthcare professionals follows the Uniform Code for Pharmaceutical Marketing Practices. We promote our products honestly, on evidence, without inducement.
- Accurate, non-misleading product claims
- Scientific exchange led by medical affairs
- No inappropriate gifts or inducements
- Internal Code of Conduct for all field staff
Pharmacovigilance & safety
Patient safety does not end at sale. We actively collect, assess and report adverse events, and cooperate with India's Pharmacovigilance Programme (PvPI).
- Dedicated pharmacovigilance mailbox: pv@sanevedahealthcare.in
- One-click "Report a Side Effect" on every page
- PvPI national helpline: 1800-180-3024 (toll-free)
- Timely onward reporting to regulators
Our quality assurance process
From raw material to the pack in a patient's hand, every step is checked.
Vendor & raw-material qualification
Active ingredients and excipients are sourced from qualified suppliers and tested on receipt.
Validated manufacturing
Production runs on validated processes in controlled, GMP-compliant environments.
In-process & finished-goods testing
Quality control checks identity, purity, potency and dissolution before release.
Stability & batch release
Each batch is released against specification, with retained samples and stability monitoring.
Traceable distribution
Batch numbers allow full traceability and rapid action if any concern is ever raised.
Registrations
Our statutory identifiers are listed below for transparency.
| Legal entity | Saneveda Healthcare Pvt Ltd |
|---|---|
| Registered office | No. 40/10, R Shamanna Res. No. 6/10, Ground Floor, SBI Layout, Bannerghatta Road, Bengaluru, Karnataka 560076, India |
| CIN | To be updated on allotment |
| GSTIN | 29ABPCS7551M1ZC |
| PAN | ABPCS7551M |
| Drug Licence Nos. | KA-B32-276043 & KA-B32-276044 |
| Pharmacovigilance contact | pv@sanevedahealthcare.in |
A question about quality or a product complaint?
Our quality and pharmacovigilance teams take every report seriously.