Introduction UQUIFA has more than fifty years experience in successfully improving and commercialising complex chemical processes for the pharmaceutical industry. Major Services Development of novel synthetic routes and optimisation of existing laboratory processes. Scale-up from Laboratory to Pilot Plant. Scale-up from Pilot Plant to commercial. Optimising laboratory developed routes of synthesis to reduce isolation steps, improve yield, reduce batch production time and eliminate the use of toxic and/or dangerous reagents. Transfer of commercial scale processes. All UQUIFA sites operate under cGMP conditions and all sites have been inspected and approved by the FDA.