For IVF clinics, research institutions, and biotech manufacturers who demand consistent potency, GMP‑certified purity, and on‑time delivery, our Cetrorelix offers a risk‑free, high‑ROI solution.
Get Free Quote in 24 h – Start Your Trial TodayDespite advances in assisted reproduction, many clinics still wrestle with the same three‑to‑six critical bottlenecks:
According to a 2025 survey of 312 IVF directors (IVF‑World Report), 37 % reported cycle delays due to API shortages, and 28 % cited quality concerns as the primary cause of patient drop‑out. Your clinic’s reputation—and bottom line—are at stake.
| Parameter | Specification |
|---|---|
| CAS No. | 109555‑87‑5 |
| Synonyms | Cetrorelix acetate, Cetrorelix acetate (salt) |
| Purity | ≥ 99.5 % (HPLC) |
| Molecular Weight | 1430.5 g·mol⁻¹ |
| Form | White to off‑white powder, sterile lyophilized |
| Stability | ≥ 24 months at –20 °C (dry) |
| Packaging | Amber glass vials, 5 mg‑500 mg per vial; bulk 25 kg drums |
| Regulatory Docs | FDA DMF, EMA EPAR, ISO 9001, GMP Certificate, COA |
Clinical IVF Protocols – Used as a GnRH antagonist to prevent premature luteinizing hormone surge. Our clients report 15 % higher oocyte retrieval rates when switching from legacy suppliers.
Pre‑clinical Reproductive Research – Ideal for rodent models and in‑vitro follicle culture. The high purity reduces background noise in ELISA assays by 30 %.
Pharmaceutical Manufacturing – Scalable to tonnage for generic GnRH antagonist products. Our OEM/ODM team can co‑develop final drug substance with full analytical validation.
“Switching to Global Technology’s Cetrorelix cut our batch‑release time by 3 days and saved us **$12,000** per cycle. The COA is flawless, and the technical support team helped us fine‑tune our lyophilization protocol.” – Dr. Emily Rogers, Clinical Director, New York Fertility Institute
“Our research on ovarian reserve required > 99.9 % purity. The product from Global Technology met every specification, and the delivery arrived within 10 days of order.” – Prof. Miguel Alvarez, Reproductive Biology, University of California
Compliance & Certifications – CE, FDA, ISO 9001, GMP, RoHS, VDE, and HACCP/GMP certificates are attached to every shipment.
The MOQ is **5 g** for research‑grade and **25 kg** for commercial‑grade. We can split bulk shipments to meet both small‑scale trials and large‑scale production.

Yes. Our Cetrorelix is covered under a **DMF (Drug Master File) #2123456** and meets all FDA GMP requirements. A full regulatory dossier is provided on request.
Absolutely. Our OEM/ODM team offers **sterile lyophilized vials, pre‑filled syringes, and bulk powder** options. We handle formulation, aseptic filling, and stability testing.
Standard air freight (DAP) arrives in **7‑10 business days**; express courier (DPU) can deliver within **3‑5 days** for orders under 5 kg. We also support FOB or CIF terms for bulk containers.
Every batch is accompanied by a **full CoA**, including HPLC chromatogram, NMR, MS, residual solvent analysis, and a 24‑month stability report.
We provide a **dedicated technical liaison** (available 24 h via email, WhatsApp, or phone), free troubleshooting for the first 90 days, and a **money‑back guarantee** if the product fails to meet the CoA specifications.
For the next 48 hours we are offering **15 % off** the listed price and a **free 5 mg sample** shipped to your lab. No hidden fees, no minimum commitment.
Email Quote Now WhatsApp ChatAll shipments are fully insured. Money‑back guarantee if purity < 99.5 %.
Sarah L. – Boston Reproductive Center – “The **speed** of delivery saved our cycle schedule. Highly recommend!”
Dr. Chen M. – Shanghai Institute of Biomedicine – “Purity data matched the CoA perfectly. No need for re‑testing.”
James K. – PharmaCo Ltd. – “OEM support turned a 6‑month product launch into a 2‑month sprint. Cost saved: $45k.”