Tesamorelin Acetate is a synthetic 44-amino-acid analogue of human growth hormone-releasing hormone (GHRH), FDA-approved for the treatment of HIV-associated lipodystrophy (excess abdominal fat accumulation in patients on antiretroviral therapy). Manufactured via SPPS with convergent fragment condensation for the 44-residue chain, characterised per Ph. Eur. peptide monograph requirements.
We maintain regulatory dossiers in the following jurisdictions for Tesamorelin Acetate-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.
Tesamorelin Acetate is supplied as a pharmaceutical-grade peptides for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Tesamorelin Acetate typically reference it under CAS Registry Number 218949-48-5.
Our Tesamorelin Acetate is manufactured under WHO-GMP and ISO 9001:2015 conditions in Pune, India. Per-batch Certificate of Analysis (CoA) is released against USP / Ph. Eur. / IP / JP specifications depending on destination market. We hold US FDA Drug Master File and EDQM Certificate of Suitability dossiers for the molecules where regulatory recognition is required; Letter of Authorization (LoA) is issued at no charge to qualified buyers.
Quote requests for Tesamorelin Acetate are turned around within 24 business hours (IST, Pune). Bulk APIs typically ship within 7-10 business days of confirmed PO; air freight to North America and Europe runs 4-5 days door-to-door. Sample agreements are signed before shipping QC-grade material to your formulation laboratory.
We export Tesamorelin Acetate to 50+ countries including the United States, Canada, Mexico, Brazil, the European Union, the United Kingdom, Japan, Australia, South Korea, the GCC and across South-East Asia. All regulatory documents (DMF / CEP / LoA) and shipping incoterms (EXW, FCA, CIP, DAP, DDP) are negotiated per buyer.
Other peptides molecules from Longshine Boi-Tech's WHO-GMP catalogue — each with active regulatory filings, audit-ready CoA, and samples available under CDA.
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