Independent quality assurance for the bioscience supply chain.
We qualify pharmaceutical-grade API manufacturers, run independent third-party testing on every batch we handle, and publish per-lot traceability to our procurement partners. No marketing claims — just verified data.
What we do
Supplier qualification
Structured vetting of API manufacturers across NMPA, FDA DMF, EU GMP, and ISO certification regimes. We maintain a live database of verified pharma-tier and CDMO-tier suppliers.
Per-batch testing
Every batch we handle is independently tested at an ISO 17025 laboratory. HPLC purity, MS identity, ICP-MS heavy metals, LAL endotoxin, Karl Fischer water content, and residual solvents.
Procurement coordination
End-to-end coordination with manufacturers across the UK, EU, US, and Asia. Capability deck collection, sample logistics, COA review, and ongoing relationship management.
Quality is the differentiator
Most of the discount end of bioscience supply skips the parts that matter — heavy metals testing, endotoxin testing, retain samples, and route-of-synthesis documentation. Our acceptance criteria reject batches outside pharmaceutical limits even when the price would justify keeping them.
Contact
- Procurement enquiries
- sourcing@peptivolabs.com
- Direct contact
- aidas@peptivolabs.com
- Registered address
- United Kingdom
We respond to manufacturer enquiries (capability decks, sample requests, pricing) within two business days. For COA reviews and quality questions, please reference the lot number in your subject line.