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Controlling and understanding your API’s crystal forms is critical not only in the early Phase of pre-clinical manufacturing but also including later phases of clinical trial manufacturing to commercialization. When new crystal forms appear of clinical trial manufacturing batches (CTM) the FDA will require prior to approval that the process can be controlled to only produce the desired polymorph. We provide the expertise to ensure each and every API manufacturing program will provide reliability and reproducibility in every CTM produced. Our partners have unsurpassed world-renowned leading scientific staff that will ensure your API program will be successful.

20 Years

Of experience serving the drug discovery market.

$100 Million

In transactions between pharmaceutical companies and our global supplier base.


Biotech programs brokered to date.

Ready to see how we can help you hit your R&D goals?

Please don’t hesitate to reach out to us today to discuss how we can help you reach your objectives.


Drug Discovery Alliances was recently certified by the Greater Womens Council and received the Women’s Business Enterprise National Council certification.

HUB Zone certification

Drug Discovery Alliances was recently HUB Zone Certified.