Tedor Pharma Services is a contract manufacturer of drug product for small and large molecules; solid and device delivered, dosage forms. We manufacture drug product from clinical phase II through large batch commercial for our worldwide clients. Tedor is a reliable outsourcing partner that utilizes decades of industry knowledge and quality manufacturing experience to help bring your product to market. Founded in 2001 and U.S. based we are headquartered in Cumberland, RI and are one hour south of Boston, MA.
Tedor Pharma Services is a contract development and manufacturing organization (CDMO). We have invested in our facility’s infrastructure and expanded our expert staff to affirm our commitment to customer success. Work with us for an easy tech transfer using our robust quality management system (QMS), and excellent regulatory track record.
Your Partner from start to finish
Whether your company has a diversified portfolio of commercialized products, you are filing for an IND, NDA, or ANDA, or you are a virtual company that has recently purchased an ANDA and wants to work out your next steps, Tedor will partner with your team to deliver end-to-end outsourcing solutions. We provide high-quality, cost competitive manufacturing services, are DEA licensed to manufacture controlled substances schedules CII through CV, and specialize in small batch, often difficult to manufacture products.
Our comprehensive solutions consist of formulation and process development, robust analytical services, and GMP manufacturing for clinical through commercial-scale production. Learn more about our service offerings:
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.
Clinical Trial Supply 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 small molecule 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.
Project Management Designed for Customer Success
Tedor’s agile team provides rapid, leadership-level responsiveness to each of our clients and a high level of attention on every size of project. Our Quality by Design (QbD) milestone-based project management process — which includes methodical assessment, analysis, and planning from day one — ensures our partners a successful outcome. We show our commitment to your goals from day one, and our four-part project management system boils down to:
Leverage our vast experience in small molecule pharmaceuticals to understand the scope of your project.
Build a custom, milestone-based plan for a thorough development or transfer process.
Execute each stage of your project and communicate our progress updates, acting as an extension of your team.
Small-batch to commercial GMP manufacture of your drug product with logistical support for a smooth path to patient.
Meet the Tedor Team
Tedor’s people are the backbone of our company. Our state-of-the-art facility is matched by our subject matter expert staff, who have the solid dose expertise necessary to guide your project.