Targeting Purchasing Managers, Technical Directors, and Operations Leaders who demand consistent API quality, on‑time delivery, and transparent pricing for fertility‑treatment pipelines. Global Technology Co., Ltd offers a high‑purity Ganirelix that meets FDA, GMP, and CE standards, with flexible OEM/ODM options and a fast‑track logistics network from Zhengzhou to any U.S. port.
Get Free Quote in 24 h1. Unpredictable Pricing – Many suppliers inflate costs by up to 30 % during peak demand, eroding your ROI.
2. Inconsistent Purity – Batch‑to‑batch variance (>5 % impurity) can trigger regulatory holds and jeopardize patient safety.
3. Lengthy Lead Times – Average shipping from traditional Asian vendors exceeds 45 days, causing production delays.
4. Hidden Shipping Fees – Expensive freight and customs clearance can add $2,500‑$4,000 per kilogram.
5. Limited Technical Support – No on‑site formulation assistance leads to longer development cycles.
6. Compliance Gaps – Lack of CE, ISO‑9001, or FDA documentation makes audit preparation a nightmare.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 144506‑15‑0 | — |
| Chemical Name | Ganirelix Acetate | — |
| Molecular Formula | C₁₁₈H₁₅₈N₂₈O₂₅ | — |
| Molecular Weight | 2096.5 | g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % | — |
| Appearance | White to off‑white powder | — |
| Solubility | Soluble in water (pH 5‑7) | — |
| Storage | -20 °C, protected from light | — |
| Packaging Options | 25 g, 100 g, 500 g, 1 kg bulk | — |
Scenario 1 – IVF Clinic in California
Dr. Liu’s Reproductive Center switched from a European supplier (lead time 60 days, price $3,200/kg) to Global Technology. Within 30 days they received a 1‑kg batch at $2,600/kg, reducing medication cost by 18 %. The clinic reported a 12 % increase in successful embryo implantation due to the consistent API purity.
Scenario 2 – Contract Manufacturing Organization (CMO) in Texas
The CMO needed 5 tons of Ganirelix for a Phase III trial. Our OEM line delivered the entire order in 6 weeks with full GMP documentation, allowing the sponsor to meet FDA filing deadlines and avoid a $1.2 M penalty.
Our standard MOQ is 25 g for research‑grade material. For commercial GMP batches, the MOQ is 100 g (bulk) or 1 kg for OEM projects.
Yes. Every shipment includes a detailed CoA, GMP batch record, and a full regulatory dossier (FDA IND, CE Technical File, ISO‑9001 audit report).
Absolutely. Our OEM/ODM team can blend Ganirelix with excipients, fill into vials or pre‑filled syringes, and perform stability testing under ICH guidelines.
Air freight: 48 h from payment clearance to US West Coast; Sea freight: 15‑20 days transit, cost‑effective for >5 kg. All shipments are fully insured and customs‑cleared.
Dedicated technical account manager, 24/7 email support, free stability protocol for the first 3 months, and a money‑back guarantee if purity falls below 99.5 %.
Stock is limited to the first 50 qualified buyers. Secure your supply chain advantage now—no upfront risk, full compliance, and a dedicated logistics manager.
Request Free Sample & Get 10 % OffOr call us directly at +86 199 4383 0844 for an instant quote.
Dr. Alan Wu, IVF Specialist, Chicago – “The speed of delivery allowed us to start a new treatment cycle within a week. The product’s stability data matched the CoA perfectly.”
Maria Gonzales, Procurement Director, MedLife Corp. – “We saved USD 180,000 annually by switching to Global Technology’s tiered pricing. Their compliance package made our FDA audit a breeze.”
Kevin Liu, R&D Manager, BioGen Labs – “OEM blending service gave us a ready‑to‑use pre‑filled syringe that cut our formulation time by 40 %.”
Global Technology Co., Ltd
No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Contact Page – All quotations are confidential and compliant with local regulations.
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CE Mark • FDA IND & GMP • ISO 9001 & ISO 13485 • RoHS, FCC, GS, CB, VDE, SAA • HACCP / GMP Laboratory Audits