We are a San Francisco Bay Area based CRO/CDMO supporting biopharma companies with customized formulations and clinical trial materials manufacturing. Our vision is to improve clinical success through customized formulations! Today, fewer than 5% of drug candidates advance from Phase 1 to clinical approval, but research has consistently shown that the right formulation strategy can increase clinical success rates by 30–40%. Formulations that control solubility, permeability, release rate, stability, scalability and patient acceptability can dramatically reduce false-negative outcomes. We are committed to advancing science-driven, tailored formulations that help innovators reach the clinic faster—and reach patients with better, safer, more effective medicines.

Our scientific belief: 
With the right formulation fit, every drug molecule can achieve clinical success and serve humanity!

Our capabilities: Preclinical to post marketed formulations - any dosage, any route, any challenge.
   
* API Characterization
* Solubility and compatibility studies of your API vs excipients
* Technical Solutions for Solubility and Permeability Challenges
* Micronizing by Milling or by creating Amorphous Solid Dispersions via Spray-Drying or HME
* Design and development of Preclinical Formulations
* Numerous Dosage Forms with a Wide Range of Release Profiles
* Preparation of Scalable Prototype Formulations of Animal PK Dosage forms for DMPK, Toxicity, or Efficacy Studies
* Analytical Studies of formulations to back up your dosage form with data pertaining to purity, stability, and dissolution profiles. 
* GLP Formulations for toxicity Assessments
* Phase 1 Manufacturing of Clinical Materials

ReechPharma

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