Twenty years inside peptide chemistry
We began as a contract synthesis laboratory and grew into a research supplier — the same bench discipline, applied at institutional scale.
Built from the bench outward
Peptide+ started in 2004 with a single synthesis line serving university laboratories that needed reliable, documented material in small quantities. The requests grew: larger scales, modified residues, conjugates, and eventually full documentation packages for institutional procurement.
Today we operate a GMP+ production footprint of 18,000 m², supply more than sixty countries and support preclinical programmes through CRO and CMO services. The operating rule has not changed: a batch is released when the data says it is ready, not when the order says it is due.
Two decades, one direction
Founded as a synthesis laboratory
One synthesis line, university customers, small-batch custom peptides.
Analytical suite added
In-house HPLC and mass spectrometry brought identity and purity testing in-house.
GMP+ facility commissioned
Move to an 18,000 m² controlled production site with formal batch records.
Independent release testing
Every batch begins release testing at an external accredited laboratory.
Authorized-seller register
Public register launched so buyers can check a reseller before placing an order.
60+ countries supplied
Catalog of 40+ compounds, custom synthesis from 5 mg to multi-gram scale.
What we will and will not do
Documented, not claimed
If a result is not in the batch record, we do not put it in marketing copy.
Research customers only
We do not sell to consumers and we decline orders that cannot be verified as institutional.
Release before schedule
Lead times are quoted from the analytical queue. We do not ship to hit a promise.
Technical support, not sales scripts
Questions go to people who can read the chromatogram and answer in plain language.
Controlled from synthesis to seal
Production, purification, lyophilization and packaging take place inside a single documented footprint. Environmental monitoring, cleaning validation and personnel training are recorded per shift.
- ISO 8 fill zone with environmental monitoring
- Electronic batch records with full audit trail
- 24-month retention samples for every batch
Institutional procurement, CRO and CMO enquiries
Tell us the compound, the scale and the documentation you need. We will respond with a concrete plan.