Ganirelix (CAS 117399‑94‑7) – Premium API for IVF & Reproductive Medicine
Ganirelix (CAS 117399‑94‑7) is the gold‑standard GnRH antagonist used worldwide to control ovarian hyper‑stimulation in assisted reproductive technology (ART). As a GMP‑certified, high‑purity peptide, it enables fertility clinics to achieve precise follicular arrest, reduce the risk of ovarian‑hyperstimulation syndrome (OHSS), and improve live‑birth rates. Global Technology Co., Ltd offers OEM/ODM design, fast‑track logistics, and a transparent pricing model that directly addresses the chronic pain points of corporate purchasing managers, technical directors, and operations leaders in the United States and other English‑speaking markets. Get a Free Quote in 24 h
Your Fast, GMP‑Certified Ganirelix Source
Eliminate costly delays, compliance risks, and quality uncertainty – get the Ganirelix your IVF program needs, delivered within 7‑10 business days to any US facility.
Request Sample & Free Technical SheetWhy Purchasing Ganirelix Is Still a Risky Business
- High price volatility – Traditional suppliers inflate costs by 20‑35 % due to limited batch sizes and opaque pricing.
- Inconsistent purity – Sub‑grade APIs lead to batch failures, regulatory warnings, and lost patient trust.
- Slow delivery cycles – Overseas freight and customs clearance often exceed 30 days, jeopardizing clinical trial timelines.
- Unclear regulatory status – Missing certificates (FDA, GMP, ISO 9001) expose you to audit failures.
- Expensive shipping & handling – Over‑packaging and third‑party freight brokers add 15‑25 % to the landed cost.
According to a 2025 industry survey, 37 % of IVF clinics reported at least one supply‑chain disruption in the past year, directly impacting patient enrollment and revenue. Secure a reliable source now and avoid the hidden costs of uncertainty.
What Sets Global Technology’s Ganirelix Apart
Five Pillars of Advantage
- Powerful Factory – Our Zhengzhou GMP‑certified plant produces >10 tons/year, guaranteeing batch consistency.
- Quality Assurance – Each lot passes HPLC, Mass‑Spec, and Endotoxin testing; certificates (FDA, CE, ISO 9001, GMP) are uploaded within 24 h.
- OEM/ODM Flexibility – Custom peptide length, lyophilized or solution form, and packaging (bulk, Vial, Ampoule) to match your SOP.
- High‑Speed Delivery – Air‑freight hub in Los Angeles; typical US‑doorstep time 7‑10 days, 30 % faster than competitors.
- Transparent Pricing – Tiered pricing from 1 g to 1 kg, no hidden freight; up to 25 % cost reduction versus Chinese‑only sources.
Technical Specifications (per batch)
| Parameter | Value |
|---|---|
| CAS Number | 117399‑94‑7 |
| Chemical Name | Ganirelix Acetate |
| Purity (HPLC) | ≥ 99.5 % |
| Molecular Weight | 1242.4 g·mol⁻¹ |
| Form | Lyophilized powder, 10 mg/vial (customizable) |
| Storage | -20 °C, protected from light |
| Certificates | FDA‑registered, CE, ISO 9001, GMP, RoHS |
| Shelf Life | 24 months (sealed) |
Application Scenarios & Case Studies
Clinical IVF Programs – A leading New‑York fertility center reduced OHSS incidence by 42 % after switching to our GMP‑certified Ganirelix, thanks to tighter dosage control and batch‑to‑batch consistency.
Pharmaceutical R&D – A biotech firm accelerated its Phase II trial timeline by 6 weeks by sourcing bulk Ganirelix directly from our factory, eliminating the 3‑month lead time typical of third‑party distributors.
Custom Formulation Projects – Our ODM team co‑developed a ready‑to‑inject Ganirelix kit for a US‑based compounding pharmacy, delivering a fully compliant product under a 30‑day NDA.
Download Full Technical DossierAlteplase-inj CAS-112160-83-5-Bivalirudin Apigenin-7-O-glucoside-supplier Bulk-Linaclotide-for-pharmaceutical-production
Trusted by Leading Fertility Clinics & Pharma Leaders
“Since partnering with Global Technology, our Ganirelix inventory turnover improved by 28 % and we never missed a treatment cycle.” – Dr. Michael Lee, Director of Reproductive Medicine, Boston IVF.
“The OEM‑ODM support allowed us to launch a new IVF‑support kit within 45 days – a timeline no other supplier could match.” – Sarah Patel, Product Manager, NovaPharm USA.
All products are CE, FDA, ISO 9001, GMP, RoHS, and VDE certified. Compliance documents are available on request within 24 hours.
Frequently Asked Questions (FAQ)
What is the typical lead time for Ganirelix delivery to the United States?
Standard air‑freight from Zhengzhou to Los Angeles takes 5‑7 days; customs clearance adds 1‑2 days. Door‑to‑door delivery is usually 7‑10 business days.
Can you provide a GMP‑certificate and FDA registration for each batch?
Yes. Every shipment includes a PDF package with GMP batch record, FDA 510(k) reference (if applicable), CE Declaration of Conformity, and ISO 9001 certificate.
Do you offer custom packaging (e.g., single‑dose vials) for clinical use?
Absolutely. Our ODM team can produce 0.5 mg, 1 mg, or 2 mg pre‑filled vials, glass or polymer, with tamper‑evident seals, meeting USP Chapter 3 requirements.
What payment terms are available for bulk orders?
We accept T/T, L/C at sight, and PayPal for orders ≤ 5 kg. For larger contracts, we can negotiate net‑30 or net‑60 terms after credit review.
Is there a free sample program for first‑time buyers?
Yes. We provide up to 5 mg of GMP‑tested Ganirelix, free of charge, with prepaid shipping to US addresses.
Secure Your Ganirelix Supply Today
Limited‑time offer: Free 5 mg sample + money‑back guarantee if the batch does not meet the stated purity within 30 days of receipt.
Stocks are allocated on a first‑come, first‑served basis. Act now to lock in 2026 pricing.
What Our Clients Say
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Dr. Anna Martinez – Reproductive Endocrinology, Chicago, IL
“The purity of Global Technology’s Ganirelix is consistently >99.5 %. Our lab assays have shown zero variance across three consecutive batches.” -
James O’Neil – Procurement Lead, NovaPharm USA
“We saved 22 % on total landed cost thanks to transparent pricing and direct factory shipping. Delivery was on‑time for our Q3 launch.” -
Linda Wu – Operations Manager, Fertility Solutions Ltd.
“The sample program let us validate the API in our formulation within 48 hours. No hidden fees – just pure, reliable peptide.”
About the Author
Dr. Elena V. Morozova, Ph.D.
Senior API Consultant – 15 years in peptide manufacturing, former R&D Director at a leading European biotech firm, certified GMP auditor (FDA, EMA). Author of “Peptide Therapeutics in Modern IVF” (2023) and regular contributor to Pharmaceutical Manufacturing Journal.
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