Process Development Services

Process Development Services
Product Description

Our team of highly skilled chemists specialize in fit-for-purpose route design of complex, multi-step organic syntheses. They leverage the extensive capabilities and diverse chemistry experience of Cayman Chemical to improve process development and accelerate innovation. Our team embraces a quality by design approach to maximize throughput and process understanding, ensuring seamless technology transfer during process scale up for CGMP manufacturing and commercialization. When project requirements change, our team can respond quickly to new project needs.

- Extensive scientific & technical expertise- Process development & optimization
- Route scouting
- Process safety assessments
- Material sourcing & vendor qualification

Cayman Chemical Company

  • Country/Region:
    United States
  • Founded:
    1980
  • On CPHI since:
    2021
  • Certificates:
    4
  • Employees:
    250 - 499
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Manufacturer/Innovator
Primary activities
Generic APIs producer
Specifications
  • Selling Points
    Price; Quality Service; Reputation
  • Supplied from
    Czech Republic; United States

Cayman Chemical Company

  • Country/Region:
    United States
  • Founded:
    1980
  • On CPHI since:
    2021
  • Certificates:
    4
  • Employees:
    250 - 499
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Manufacturer/Innovator
Primary activities
Generic APIs producer

More Products from Cayman Chemical Company (20)

  • GMP Psilocybin

    Product GMP Psilocybin

    Psilocybin is manufactured at Cayman Chemical in Ann Arbor, MI via a fully synthetic route. GMP material appropriate for clinical trials is available.
  • GMP SM-102

    Product GMP SM-102

    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.)
  • GMP Tafluprost

    Product GMP Tafluprost

    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.
  • GMP Travoprost

    Product GMP Travoprost

    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.
  • GMP Y-27632 (hydrochloride) Ancillary Material

    Product GMP Y-27632 (hydrochloride) Ancillary Material

    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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  • IWR-1-endo Ancillary Material

    Product IWR-1-endo Ancillary Material

    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...
  • Y-27632 (hydrochloride) Ancillary Material

    Product Y-27632 (hydrochloride) Ancillary Material

    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...
  • Bucladesine (sodium salt) Ancillary Material

    Product Bucladesine (sodium salt) Ancillary Material

    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 veter...
  • DAPT Ancillary Material

    Product DAPT Ancillary Material

    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 veter...
  • GMP (+)-Cloprostenol sodium salt

    Product GMP (+)-Cloprostenol sodium salt

    (+)-Cloprostenol sodium salt is manufactured at Cayman Pharma, our Czech subsidiary. GMP material is available, and the ASMF for (+)-Cloprostenol sodium salt is on file in the UK, Switzerland, and in most EU countries.
  • GMP (±)-Cloprostenol sodium salt

    Product GMP (±)-Cloprostenol sodium salt

    (±)-Cloprostenol sodium salt is manufactured at Cayman Pharma, our Czech subsidiary. GMP material, which conforms to the USP and BVP Monographs, is available. The DMF is on file with the US FDA, Canada, Russia, in almost all EU member states, and in many other countries.
  • GMP (−)-(R)-Methamphetamine (hydrochloride)

    Product GMP (−)-(R)-Methamphetamine (hydrochloride)

    (-)-(R)-Methamphetamine (hydrochloride) is manufactured at Cayman Chemical in Ann Arbor, MI. GMP material appropriate for clinical trials is available.