CDMO Services

End-to-End NCE Development & Custom Manufacturing

At Synergene Active Ingredients, we prioritize client goals by working as a collaborative CDMO partner to ensure project success. We offer an end-to-end continuum of customized New Chemical Entity (NCE) development services, supporting small molecules from early-stage lab route scouting through to large-scale commercial cGMP supply.
With over 40 years of industrial chemistry experience, state-of-the-art infrastructure, and a strong regulatory track record, we help pharmaceutical and biotech companies de-risk process development, shorten time-to-market, and optimize manufacturing economics.

Core CDMO Offerings

Chemistry & Process Development
Designing efficient, scalable, and robust synthetic routes.
Analytical Development & Validation
Advanced analytical methods development to support regulatory filings.
Process Safety & Engineering
Comprehensive thermal, hazards, and reaction assessment for safe scale-up.
Phase-Appropriate Development
Tailored solutions meeting regulatory requirements from Pre-Clinical through Phase III trials.

Custom Manufacturing

Our flexible, cGMP-compliant manufacturing units support seamless scale-up from kilogram batches to commercial multi-ton volumes.
Dedicated pilot plants and commercial reaction capacity.
Expertise in complex, multi-step chemical synthesis.
Stringent quality systems ensuring full compliance with global standards.