Discover Aceto's extended Biopharma portfolio at CPhI North America


Aceto will exhibit at CPhI North America from May 17th to 19th in Philadelphia where we will launch our newly extended biopharma product portfolio, which now includes:


  • GMP excipients
  • Wide range of GMP raw materials
  • Biological buffers
  • Buffering salts
  • Process and cleaning solutions
  • APIs
  • Amino acids
  • Nucleotides
  • Cofactors
  • Water for Injection for further processing
  • Cell culture ingredients
  • IVD ingredients


We are specialized in providing tailored solutions to pharma & biopharma finished drug manufacturers through an innovative and highly personalized approach.  Learn more about our biopharma offering

Our tailored services include GMP custom ingredient development, GMP custom manufacturing, GMP custom packaging & repacking, regulatory support and analytical services. 


For all those who will attend CPhI North America, we would be delighted to meet you there and discuss with you the challenges & requirements of your manufacturing processes, to find out how Aceto can help you find the best customized solution for you.


Email us to book a meeting with our team, or stop by our booth #1105 (Informex Zone) at CPhI



Founded in 1947, Aceto is leading global supplier of niche, differentiated specialty materials for the life sciences and advanced technology end markets. 
With business operations in over ten countries, Aceto supplies over 3,000 chemical compounds used principally by the pharmaceutical, nutraceutical and specialty chemical industries. 
Aceto’s global operations include R&D, GMP manufacturing facilities, significant on the ground sourcing at strategic locations globally, and strong partnership with key suppliers and manufacturers. 

Through our integrated centers of excellence facility network in North America, Europe and Asia, Aceto is a global GMP manufacturer of raw materials suitable for biopharmaceutical applications. 

Aceto is renowned for our high quality standards and provides full transparency in the supply chain, which is vital for compliance with GMP and GDP. We hold all major certifications and applicable licences from the main accreditation bodies and agencies

We perform routine and non-routine analytical testing for biopharmaceutical products, in support of manufacturing processes, QA/QC functions, R&D projects, and environmental applications. 
Leveraging state-of-the-art instrumentation

Aceto’s global GMP manufacturing facilities allow us to complete a variety of projects simultaneously with rapid response and completion times. Thanks to our Partner Service Organization approach, our partners experience R&D, project management, GMP documentation and production lead times that surpass the industry norm. 

Find out more about Aceto