API and pharmaceutical intermediates manufacturer. Track record in both developmental and generic API manufacturing. Process R&D through to commercial production under cGMP. CMC services. FDA inspected US facilities. DEA registration. ISO 7 cleanroom. Parallel resources at Shanghai Chemspec with US project management. Operating in Fairfield, NJ since 1997, Chemspec-API provides expertise and FDA inspected facilities that will take your product through process R&D to production under cGMP. Special experience: Fluorine Chemistry SMB separations Continuous processing (with Proteaf Technologies: www.proteaf.com) Enquiries: info@chemspec-api.com