Project planning and regular communication are utilized to ensure that customer expectations of quality and delivery are met. Manufacturing is conducted by an experienced staff of technicians, Bachelor–degreed and Ph.D. chemists.
Custom Synthesis work is provided over a broad range of reactions, including those requiring the use of high pressure reactors and conditions. Pilot–scale quantities can also be supplied.
For pharmaceutical applications, manufacturing of API's (active pharmaceutical ingredients) and intermediates is conducted under current Good Manufacturing Practices (cGMP) in our kilo–lab facility (class 10,000) which has been operational since 1988.
Complete documentation is available for manufacturing under cGMP including validation of stability studies. Active Drug Master Files (DMF's) are maintained in over 20 countries including USA, Europe and Australia (see below).
Additional products have been made under cGMP where no public regulatory filing is available.