


Senova Tech - CDMO/CMO
Senova Technology is a leading & professional supplier for APIs/Advanced Intermediates/CMO products & service based on our high level R&D center (in Hangzhou) and GMP approved facility (in Shaanxi).
Over the past 8 years, thanks to our partners and customers support, Senova has had a high speed development with 30% increase in sales turnover per year, and now our customers spread over Asia/Europe/Middle Eastern market.

China

ISO9001 certified

Drug R&D center (in Hangzhou)

From lab scale (mg/g) to commercial scale (kgs/tons)
Our services:
Production scale:
Response time:
Services
Drug Substance (CDMO/CRO)
Replies quickly
Replies quickly
Replies quickly
Contact Senova Technology Co., Ltd. for Contract Services Expertise
Connect with Senova Technology Co., Ltd., a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO). Contact Senova Technology Co., Ltd. for free and discover if they are the perfect partner for your pharmaceutical needs.
Drug Substance (CDMO/CRO)
Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.
Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.
Key Functions of Drug Substance CDMOs/CROs:
API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.
Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.
GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.
Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.
Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.
Explore Leading API CDMOs and CROs
Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.