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.  (803) 442-7590


    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