We offer Comprehensive GMP Peptide Manufacturing.  The GMP manufacturing professionals at TirzepatidePharma have over 50 years of cumulative experience in peptide process development, scale-up, and cGMP (Current Good Manufacturing Practice) standards, as defined by the FDA.  We manufacture peptides using solution-phase (liquid-phase or LPPS), solid-phase peptide synthesis (SPPS), or hybrid processes.

The minimum quantity for FDA-registered peptides with Methyl Vitamin B12 (1000mcg API)/ml is 50,000 packs for companies interested in ANDA drug application.  Manufactured with approved DMF according to the Federal Food, Drug, and Cosmetic Act for commercial distribution, ANDA registration, or clinical trials. Not affiliated, endorsed, or intended to replace Eli Lilly, Novo Nordisk, or other companies' or FDA-approved brands such as Victoza, Saxenda, Byetta, Ozempic, Rybelsus, Wegovy, Adlyxin, Trulicity, or Mounjaro.