Have It Made
Our expertise lies in the reliable manufacture of high quality solid dose pharmaceuticals and controlled substances. From IND, NDA, or ANDA to commercial manufacture, our comprehensive and flexible services provide speed, quality and efficiency on the path to patients.
Clinical Trial Services
Leverage our expertise in clinical trial guidance to support the entire drug development process, including clinical trial dosage form, placebo manufacturing, quality assurance, and clinical supply chain management.
We provide GMP manufacturing of solid dose pharmaceuticals at ranging scales from small-batch to large-scale commercialization with our purpose-built facility and expert staff.
Produce stable, effective drug delivery platforms for active pharmaceutical ingredients (APIs) with our high-quality process development and validation services.
Our multiple, well-fitted GMP laboratories ensure we meet FDA compliance requirements for characterization, testing, analytical development and quality assurance, from pre-formulation to commercialization.
Tedor Pharma Services is a reliable, US-based contract development and manufacturing organization (CDMO) with 20+ years of experience in solid dosage forms. Headquartered in Cumberland, RI (an hour south of Boston, MA), our expert staff will partner with your team to provide guidance and flexible, end-to-end outsourcing solutions for your small molecule drug product.
Flexible Services to Meet Your Needs
Our state-of-the-art facility has an excellent regulatory track record and provides GMP manufacturing for every step of your solid dose drug product’s journey. We are FDA registered and inspected, and DEA licensed to manufacture controlled substances schedules II through V.