Assessment


Submit Requirements

How should we reach you? (required)
EmailPhoneEither

Do you have a peptide which is being developed as a potential new chemical entity which will require cGMP synthesis which you would like AmbioPharm to quote? (required)
YesNo

Do you have a budget for this project? (required)
YesNo

Would you like to sign a Nondisclosure Agreement so that we can learn more about your project and it’s requirements to further our discussions? (required)
YesNo

Do you have a need for custom peptide synthesis under non-GMP conditions for your research program?(required)
YesNo

Are you interested in learning more about our generic active pharmaceutical ingredients (APIs)? (required)
YesNo

Do you need methods validation, stability studies or other analytical testing for your peptide API? (required)
YesNo

Questions for our GMP peptide expert

Hi, this is Jim Hampton, Executive VP of Business Development. Please call me to discuss any aspect of GMP manufacturing of peptides for clinical studies and leave a message.  (415) 921-3593


Questions for our Regulatory and Generics Departments

Regulatory Affairs Department
Phone: (803) 442-7590
Generics Department

Please click here to download our standard NDA


USA Headquarters

AmbioPharm, Inc.
1024 Dittman Court
North Augusta, SC 29842

Phone: (803) 442-7590