WHO
GMP
GMP
WHO-GMP Aligned
Facility design, hygiene, documentation and process controls aligned with Good Manufacturing Practices.
Certifications
Compliance-led systems that protect product quality and partner confidence.
Quality Framework
Standards we manufacture to
Our operations are structured around globally recognised pharmaceutical quality practices and Indian regulatory expectations.
ISO
9001
9001
ISO Quality Systems
Process orientation, continual improvement and measurable quality objectives across functions.
GLP
Good Lab Practices
Reliable analytical testing, calibrated instruments and retained sample discipline.
Drug
Licence
Licence
Licensed Operations
Manufacturing under applicable drug licences for oral dosage formulations.
Assurance
How quality is built in
Quality at Sucantis is not a final checkpoint — it is a chain of controls from vendor qualification to dispatch.
- Approved vendor lists for critical materials
- Incoming material identity and quality checks
- In-process controls during manufacturing
- Finished goods testing before release
- Batch manufacturing and packing records
- Stability and complaint handling procedures
Documentation
Traceability you can audit
Partners receive the documentation support expected in regulated manufacturing relationships — SOPs, batch records, COAs and change-control visibility as applicable.
Our teams are trained to treat every document as part of the product: accurate, contemporaneous and reviewable.
Need certificates for a tender or audit?
Share your requirement and our team will respond with the latest available documentation.
Contact Quality Team