GMP Psilocin

Bimatoprost is manufactured at Cayman Pharma, our Czech subsidiary. GMP material is available, and the DMF for Bimatoprost is on file with the US FDA, Canada, and India.

DMT Hemifumarate is manufactured at Cayman Chemical in Ann Arbor, MI via a fully synthetic route. GMP material appropriate for clinical trials is available.

Epoprostenol sodium salt is manufactured at Cayman Pharma, our Czech subsidiary. GMP material is available, and the DMF is on file with the US FDA, Canada, Japan, Australia, and many EU member states.

This product has been manufactured and tested in accordance with GMP principles set forth by the ICH and FDA and meets the expectations for commercial cell, gene, and tissue-engineered products in accordance with USP <1043> “Ancillary Materials for Cell, Gene, and Tissue-engineered Products”.
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Latanoprost is manufactured at Cayman Chemical in Ann Arbor, MI and at Cayman Pharma, our Czech subsidiary. GMP material from both Cayman Chemical and Cayman Pharma, which conforms to the USP, EP, and IP Monographs, is available. Each site maintains a unique DMF; they have been filed with the US FDA, Canad...

Latanoprostene Bunod is manufactured at Cayman Pharma, our Czech subsidiary. GMP material is available, and the DMF for Latanoprostene Bunod is available for customer review upon request.

Psilocybin is manufactured at Cayman Chemical in Ann Arbor, MI via a fully synthetic route. GMP material appropriate for clinical trials is available.

M-102 is manufactured as an excipient suitable for use in LNP preparation and small molecule encapsulation at Cayman Chemical in Ann Arbor, MI. GMP material appropriate for clinical trials is available. (NOTE: This product is subject to licensing for use in commercial applications.)

Tafluprost is manufactured at Cayman Pharma, our Czech subsidiary. GMP material is available, and the DMF for Tafluprost is available for customer review upon request. The DMF has been filed with the US FDA and in Russia.

Travoprost is manufactured at Cayman Pharma, our Czech subsidiary. GMP material, which conforms to the USP Monograph, is available. The DMF is on file with the US FDA, Canada, India, Japan, China, in several EU member states, and in several other countries.

This product has been manufactured and tested in accordance with GMP principles set forth by the ICH and FDA and meets the expectations for commercial cell, gene, and tissue-engineered products in accordance with USP <1043> "Ancillary Materials for Cell, Gene, and Tissue-engineered Products.
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This product has been tested in accordance with GMP principles and meets the expectations for clinical cell, gene, and tissue-engineered products in accordance with USP <1043> “Ancillary Materials for Cell, Gene, and Tissue-engineered Products”.

WARNING This product is not for human or vet...