To lots of APIs (especially the Generic ones) we are doing:

Synthesis process selection→intermediates quality control→setting up analytical method for APIS→DMF documents compiling→CGMP Manufacturing 

We can support you the key technology and quality documents with validation for API synthesis free of charges under the condition that CDA and some related contracts have been signed by two parts. 

We are developing Olopatadine, Voriconazole and Darifenacin etc. as per the above guidelines. You are welcome to discuss with us!

         Voriconazole                            Olopatadine,

                      Darifenacin