Advancing Drugs

 Call for a consultation  202-780-4988

Custom API Synthesis or cGMP scale-up?

(U.S. based contract laboratory)   


                                         Contact us to discuss today 

Manufacturing operations performed on a routine basis

  • High & low temperature chemistry    
  • Pressure reactions    
  • Extractions  
  • Freeze-drying
  • Column purifications / Flash Chromatography    
  • Preparative HPLC     
  • Distillations    
  • Spray-drying
  • Formulation and component preparation
  • Filling, labeling and packing
  • Development and Clinical Trial Materials
  • QC testing and release





         Cost benefit Model


We provide quality API synthesis and process scale-up at competitive pricing while providing help to our clients through every step of the process.  





We provide quality custom synthesis and pharmacetical manufacturing for novel compounds and intermediates.  We provide scale up to kilogram quantities.   

We oversee all the quality and stability testing on all products manufactured and provide a CoA (Certificate of Analysis) for all product being supplied.  This means you can purchase from a U.S. manufacturer and not have to deal with the issues associated with purchasing and verifying quality with overseas manufacturers.  


Providing the following drug development services

  • ​​​Design and synthesis of novel compounds
  • Synthesis of analogs of lead compounds
  • Chemical synthesis process development and optimization
  • Formulation development and optimization
  • Analytical method development and validation
  • cGMP manufacturing of APIs with all routes of     administration including topical, oral, and injectable
  • Stability studies for APIs/intermediates and drug products
  • Documentation for all stages of drug development



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Pharmaceutical Manufacturing