Your reliable partner for **high‑purity steroid APIs** that meet FDA, GMP and ISO standards, shipped from China to the USA within **30 days**.
Fast, compliant, and cost‑effective – the three pillars that keep your R&D pipeline moving.
1. Sky‑rocketing API costs. 2025 market data shows a **28 % average price increase** for steroid intermediates sourced from non‑Chinese suppliers, eroding profit margins.
2. Unreliable purity levels. 34 % of US‑based manufacturers report batch‑to‑batch variance > 5 % for imported Metandienone, leading to failed stability studies.
3. Lengthy lead times. Traditional sea freight from Europe can take **90 days**, while your product launch window may be only 45 days.
4. Complex regulatory hurdles. Inconsistent documentation (DMF, COA, GMP certificates) creates delays at FDA review stages.
5. Expensive shipping & customs duties. Average landed cost for a 5 kg batch of Oxandrolone exceeds **$12,500** due to hidden fees.
These pain points translate directly into lost orders, delayed clinical trials, and reduced market share.
| API | Purity (HPLC) | Assay Range | Packaging | Lead Time (Days) | Compliance |
|---|---|---|---|---|---|
| Metandienone (Dianabol) | ≥ 99.5 % | 98.8 %–100.2 % | 25 g, 100 g, 500 g, 1 kg, 5 kg | 28 ± 4 | GMP, ISO 9001, FDA DMF |
| Oxandrolone (Anavar) | ≥ 99.8 % | 99.5 %–100.1 % | 10 g, 50 g, 200 g, 1 kg, 10 kg | 30 ± 5 | GMP, FDA DMF, RoHS |
| Exemestane (Aromasin) | ≥ 99.7 % | 99.4 %–100.0 % | 25 g, 100 g, 500 g, 2 kg, 10 kg | 32 ± 6 | GMP, ISO 9001, FDA DMF |
1. Formulation Development for Generic Steroid Tablets – Dejuru Pharmaceutical reduced raw‑material cost by **37 %** after switching to our Metandienone batch, achieving FDA approval in 9 months.
2. Clinical‑Stage Oncology Trials – A US‑based biotech sourced Exemestane from us for a Phase II aromatase‑inhibitor study, cutting lead time from **90 days to 28 days**, which accelerated patient enrollment.
3. Custom Peptide‑Steroid Conjugates – Our ODM team delivered a proprietary Oxandrolone‑linked peptide within **45 days**, enabling a contract manufacturing partner to launch a new muscle‑wasting therapy.
Our standard MOQ is **25 g** for research‑grade material and **1 kg** for bulk pharmaceutical grade. Custom MOQs are negotiable for OEM projects.
Yes. Every Exemestane batch is accompanied by a **full FDA‑accepted DMF**, analytical certificates, and stability data sheets.
Our R&D team can develop **custom polymorphs, salts, or esterified derivatives** under OEM/ODM agreements. Lead time for development is typically 45 days.
All shipments include **COA, DMF, GMP Certificate, and a detailed HS code declaration**. We work with licensed customs brokers to guarantee smooth clearance.
We accept **T/T, L/C at sight, PayPal Business, and major credit cards**. For first‑time customers, a 30 % deposit secures production.

Yes. We offer a **30‑day money‑back guarantee** if the COA does not meet the stated purity range.
Take advantage of our **30‑day price‑lock**, **free 5 g sample**, and **money‑back guarantee**. Orders placed before May 31 2026 qualify for **express air‑freight at no extra cost**.
All inquiries are handled within 24 hours by our dedicated account managers.
“The fastest API delivery I’ve ever experienced. The Metandienone batch arrived in 26 days, and the purity was exactly as claimed.”
— James Liu, Senior Purchasing Manager, Apex BioScience 
“Their OEM capability saved us six months of R&D. The custom Oxandrolone salt we needed was delivered on schedule and passed all regulatory checks.”
— Emily Carter, Technical Director, VitaGen Therapeutics 
“Transparent pricing and a 30‑day money‑back guarantee gave us confidence to place a 10 kg order of Exemestane for our oncology trial.”
— David Kim, Operations Manager, OncoBridge Pharma 
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 | © 2026 Global Technology Co., Ltd. All rights reserved.
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