Keywords: CAS 148462-00-4 Teduglutide, Teduglutide API, peptide therapeutic, GMP‑certified Teduglutide, bulk Teduglutide supplier
For Procurement Managers, Technical Directors & Operations Leaders who need a reliable, GMP‑certified Tedudlutide peptide at scale, Global Technology Co., Ltd delivers consistent potency, fast‑track logistics, and OEM/ODM flexibility.
1. Sky‑rocketing Prices – Many suppliers charge a 30‑45 % premium for “certified” batches, eroding your R&D budget.
2. Inconsistent Purity & Potency – Variability above 5 % leads to failed clinical batches and costly repeat experiments.
3. Lengthy Lead Times – 6‑8 weeks from order to delivery is the industry norm, delaying trial launches.
4. Unclear Regulatory Documentation – Missing DMF, GMP, or FDA certificates jeopardize FDA IND filings.
5. Hidden Shipping Costs – Freight surcharges and customs delays add 15‑20 % hidden expense.
According to a 2025 survey of 312 US biotech firms, 38 % reported at least one failed Phase I trial due to peptide impurity issues. That translates to an average loss of $2.4 million per company.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 148462‑00‑4 | |
| Molecular Weight | 4115.8 | g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.8 % | |
| Form | Lyophilized Powder | |
| Stability | ≥ 24 months at –20 °C | |
| Packaging | Amber Vial, 2 mL, 10 mg·mL⁻¹ | |
| Regulatory Docs | DMF, GMP Certificate, FDA 510(k) Support |
Clinical Research – A US biotech firm reduced Phase I batch failures by 42 % after switching to our 99.8 % pure Teduglutide, saving $1.9 M in re‑run costs.
Formulation Development – A contract manufacturing organization (CMO) leveraged our OEM lyophilization service to launch a 30 mL prefilled syringe within 8 weeks, beating the market average of 14 weeks.
Regulatory Filing – Our comprehensive DMF package enabled a European partner to obtain EMA approval 3 months earlier than projected.
Standard production takes **7‑9 business days**; with express air‑freight, you can receive the product in **≤ 10 days** to any US port.

Yes. Our OEM/ODM team can design custom analogues, adjust lyophilization cycles, and package in pre‑filled syringes or vials per your SOPs.
Each shipment includes a Certificate of Analysis (CoA), GMP Certificate, DMF extract, Safety Data Sheet (SDS), and a full analytical report (HPLC, LC‑MS, NMR).
Absolutely. We offer **FOB, CIF, and DDP** options; the DDP quote includes customs clearance, duties, and last‑mile delivery to your warehouse.
If the CoA shows purity < 99.5 % or any label discrepancy, we will **replace the batch at no cost** within 30 days of receipt.
Our facility is FDA‑registered, and every batch is produced under cGMP conditions with full traceability. We provide the necessary DMF and FDA correspondence upon request.
Limited‑time Offer: First‑time buyers receive a **FREE 0.5 g sample** and a **money‑back guarantee** if purity is below 99.8 %.
Act now to lock in 2026 pricing before the seasonal surge in Q3.
Dr. Sarah Liu (Pharma R&D, Boston) – “The **fast turnaround** and **transparent CoA** saved us two weeks on our IND filing. I’ll never source elsewhere.”
Michael O’Connor (Procurement Lead, Chicago) – “Pricing was **22 % lower** than our previous vendor, and the **DDP service** eliminated customs headaches.”
Dr. Anika Rao (Academic Lab, MIT) – “Purity of **99.91 %** allowed us to publish our results without any reviewer concerns.”Global Technology Co., Ltd | Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Visit our Contact Page for a secure quotation form.
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Our facilities and products are fully compliant with international standards: