Today we offer custom organic synthesis, contract process R&D and cGMP manufacturing of milligram to multi-kilo lots of intermediates and active pharmaceutical ingredients to the pharmaceutical, medical device, diagnostic and semi-conductor industries as well as other industries where scale-up and small lot manufacturing services from a reliable vendor with excellent quality systems is important.
Over the years, Seres has listened to clients and developed the following business practices and employee knowledge base:
- Rapid CDA, proposal and contract turnaround
- R&D and cGMP with a scale-up mentality
- Ready access to decision makers
- Professional, yet flexible business and quality systems
- Non-competitive protection for customer IP
Seres has established a comprehensive and well-tested Quality and SOP system through many years of consultation with pharmaceutical clients and the FDA. We are regularly audited by the FDA and the California Department of Health Services, Food and Drug Branch. Seres undergoes many quality audits every year from our clients and we would be glad to schedule one from your company.
To maintain Seres as a full-service, yet low overhead supplier, analytical methods development and testing is handled in-house or outsourced as appropriate to qualified and audited external laboratories.
Seres offers a link to larger volume scale-up services through full scale manufacture via an equity connection with Dixie Chemical Co. and its DX Pharma Division.
Listening, understanding and responding accurately to your business and technical needs . . . that’s the Seres advantage.
