From development batch to GMP supply.
The final step from first binder to medicine. We manufacture peptide APIs under GMP at SMS Pharmaceuticals’ Unit 7 in Visakhapatnam, an internationally approved API site, with its quality systems behind every batch.
Unit 7, Visakhapatnam.
SMS Pharmaceuticals’ flagship multipurpose API facility, and the home of our dedicated peptide plant.
SMS Peptides operates within Unit 7, SMS Pharmaceuticals’ flagship API site in Vizag. The site has a 3,000 KL reactor capacity and a strong inspection record, most recently a USFDA inspection in December 2025.
A dedicated peptide manufacturing plant is coming up on the site, built on the same quality systems that support every SMS Pharmaceuticals approval.
The Vizag site’s regulatory approvals include:
- Established quality management and change-control systems
- Experienced QA and QC teams used to regulatory audits
- Customer audits welcome
See SMS Pharmaceuticals in action.
The SMS Pharmaceuticals corporate film shows the people, sites and quality culture behind every batch we make.
About our parent company →
Corporate video · SMS Pharmaceuticals
Manufacturing built on the work that came before.
Because the same team develops your process and manufactures your API, nothing gets lost in transfer.
Scale-up & technology transfer
We take the route from development scale to manufacturing scale, transferring processes and analytical methods with full documentation.
GMP API manufacturing
Multi-kilogram quantities of final peptide API per month under GMP, for clinical trials and commercial supply.
Quality control & release
Validated analytical methods, batch release testing and certificates of analysis for every lot.
One partner from first binder to GMP batch.
- 01No hand-offs
The chemists who developed your route support its scale-up and manufacture.
- 02Pharmaceutical quality systems
Documentation, change control and compliance practices from SMS Pharmaceuticals, proven in regulated markets.
- 03Regulatory support
Batch records, quality data and documentation to support your regulatory filings.
- 04Clinical supply, coordinated
Clinical trials run by a trusted clinical partner under our coordination, while we keep supplying GMP material.
- 05Room to grow
Capacity planned to grow from clinical batches to commercial volumes.
Ready to scale up?
Tell us about your molecule, the quantities you need and your timelines, and we’ll plan the route to GMP supply together.