A Contract Development and Manufacturing (CDMO) service provides integrated, end-to-end services that support pharmaceutical companies throughout the drug development lifecycle—from early R&D through clinical and commercial GMP manufacturing. CDMO services offer scientific, technical, and operational expertise that enables efficient development, streamlined scale-up, and reliable production of starting materials, intermediates, and drug substances. By leveraging specialized capabilities, advanced infrastructure, and regulatory proficiency, CDMO services help accelerate timelines, reduce costs, and ensure consistent quality and compliance across all development stages.
Key Deliverables
- Route scouting and process development for starting materials, intermediates, and drug substance
- Scale-up and tech transfer from laboratory to pilot and commercial facilities
- GMP manufacturing for clinical and commercial supply
- Analytical method development, validation, and quality control testing
- Regulatory documentation support, including CMC packages for IND/IMPD/NDA/DMF submissions
- Supply chain management, including raw material sourcing and batch release