The company utilizes third-party manufacturers and contract manufacturing organizations (CMOs) to supply raw materials, active ingredients, and finished products for preclinical studies and clinical trials. These CMOs adhere to FDA requirements, including Good Laboratory Practices (GLP) and current Good Manufacturing Practice (cGMP) guidelines. The company has agreements with Tay, comprising an Evaluation and Option Agreement and a License Agreement for Tay's BET inhibitor compounds. Under these agreements, Tay provides data packages and chemical entity candidates, while the company manages development, regulatory, marketing, and commercialization activities for the licensed products.
Vyne Therapeutics Inc's Comment on Supply Chain
The company utilizes third-party manufacturers and contract manufacturing organizations (CMOs) to supply raw materials, active ingredients, and finished products for preclinical studies and clinical trials. These CMOs adhere to FDA requirements, including Good Laboratory Practices (GLP) and current Good Manufacturing Practice (cGMP) guidelines. The company has agreements with Tay, comprising an Evaluation and Option Agreement and a License Agreement for Tay's BET inhibitor compounds. Under these agreements, Tay provides data packages and chemical entity candidates, while the company manages development, regulatory, marketing, and commercialization activities for the licensed products.
Sources:
Vyne Therapeutics Inc 's official press releases and regulatory filings; CSIMarket.com's supply-chain research; and the financial filings and press releases of other companies cited in this report.
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