ReechPharma LLC


ReechPharma is a formulation development company located in the San Francisco Bay Area, specializing in customized formulation solutions to address each drug's unique physicochemical, biopharmaceutical, IP, and regulatory challenges. With over 60+ years of combined experience, they support pharma and biopharma companies through discovery, preclinical, clinical, and life cycle management products, offering a wide range of services including preclinical formulations, clinical formulations, life cycle management, drug-device combination products, and expert consulting. Their mission is to improve clinical success rates through tailored formulations and innovative drug delivery systems.

Industries

biotechnology
consulting
medical
pharmaceutical

Nr. of Employees

small (1-50)

ReechPharma LLC

Newark, California, United States, North America


Services

Preclinical formulation services

Formulation and analytical services to support preclinical studies, including preformulation, prototype formulations for DMPK/Tox/Efficacy, solubility/permeability solutions, and GLP formulation supply.

Clinical formulation services

Development and scale-up of clinical dosage forms across immediate, modified and extended release oral forms, liquids, semisolids and novel delivery systems for First-in-Human through late-stage clinical development.

Life cycle management and reformulation

Formulation redesign and development for label expansion and lifecycle claims such as pediatric formulations, modified release/PK modification, new routes of administration, fixed-dose combinations and novel delivery systems.

Drug-device combination product services

Pharmaceutical formulation and characterization for drug-device combination products, including compatibility/interaction studies, drug release kinetics and ICH stability testing.

Expert consulting and advisory (Reech Expert Connect)

Access to subject-matter experts for candidate selection, biopharmaceutics/PK, analytical development, regulatory submissions, technology transfer, GMP audits, manufacturing scale-up and IP strategy.

Expertise Areas

  • Formulation development (preclinical through clinical)
  • API preformulation and characterization
  • Solubility and permeability enhancement
  • Dosage form development (oral, liquid, semisolid)
  • Show More (8)

Key Technologies

  • Hot-melt extrusion
  • Nanomilling / particle size reduction
  • HPLC / UPLC analytics
  • Dissolution testing (multimedia, biorelevant)
  • Show More (5)

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