CDMO R&D and Production Services
One-Stop Solution for Small Molecule Drug CDMO
}
API & Intermediates CDMO Service
Time: 2022-03-15
Source: Viva Biotech
Share:
[Abstract]:

 

  • Synthetic route design and selection
  • Process development & optimization
  • Tox batch manufacturing
  • API analytical method development and validation
  • API stability study
  • GMP manufacturing for Phase I, II and III clinical trials
  • Scale-up and commercial manufacturing (mg to 1000 ton)
  • API CTD document preparation for IND and NDA filings
Media contact: vivapr@vivabiotech.com
Contact Us