The companies I have listed are capable of multistep small
molecule cGMP synthesis. As is the case with contract drug manufacturers,
cost, quality, and level of GMP compliance varies greatly. Due to the many details
concerning the characteristics properties of the reactions, the intermediates of the final compound, successful project management of outsourced synthesis projects requires, in my opinion,
the direct involvement of the chemist who developed the process internally.
Many times it is prefererable for the chemist to attend the synthesis
as many details are not often captured into the batch record.
Cedarburg Laboratories, Inc.�s mission is to satisfy the needs of our customers by providing laboratory to pilot scale custom manufacturing of active pharmaceutical ingredients and pharmaceutical intermediates according to cGMP guidelines