---
name: ReechPharma, LLC
slug: reechpharma
site: cro
website_domain: reechpharma.com
summary: Specializes in customized formulation development and drug delivery systems for preclinical and clinical stages, supporting drug discovery and biotech companies with GLP/GMP manufacturing and analytical services. Headquartered in South San Francisco, United States.
tagline: Customized formulation development for preclinical and clinical drug programs.
founded_year: 
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: US
tier2_domain_verified: false
updated_at: 2026-10-13T07:03:22.144Z
services_count: 8
modalities_count: 1
indications_count: 0
locations_count: 1
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# ReechPharma, LLC

Customized formulation development for preclinical and clinical drug programs.

Listed on cro.directory.

## Summary

Specializes in customized formulation development and drug delivery systems for preclinical and clinical stages, supporting drug discovery and biotech companies with GLP/GMP manufacturing and analytical services. Headquartered in South San Francisco, United States.

## At a glance

- HQ country: US

## Services

- Analytical Method Development & Validation
- ICH Stability Studies
- Translational Research
- Phase I Clinical Trials
- Phase II Clinical Trials
- Phase III Clinical Trials
- Preclinical In Vitro Studies
- In Vivo PK / PD Studies

## Modalities

- Small Molecule

## Locations

- Headquarters, South San Francisco, California, United States

## Long description

ReechPharma is a formulation research and development company offering customized drug product development solutions to address physicochemical, biopharmaceutical, intellectual property, and regulatory challenges in compliance with FDA and global regulations.

## Core Services

**Preclinical Formulations:**
- API characterization (solubility, stability, thermal and morphology analysis)
- Preformulation studies (compatibility, chemical and physical characterization, stability evaluation)
- Design and development of preclinical formulations for efficacy testing, animal PK/DMPK studies, and GLP toxicity assessments
- Dosage form development (immediate release, modified/extended release, nano-particle solutions, semisolids)

**Clinical Formulations:**
- Prototype formulations for first-in-human studies
- Phase-appropriate dosage form design
- GLP/GMP supplies for animal studies and Phase I manufacturing
- Pediatric and geriatric formulations

**Analytical Services:**
- Drug release profile and dissolution testing
- Stability storage and testing
- Analytical testing and release of API and dosage forms

## Infrastructure & Expertise

The company operates cleanrooms and maintains equipment including Nanomill, hot melt extruder, HPLCs, UPLC, dissolution/disintegration testers, UV spectrometer, stability chambers, and scanning electron microscope. The team combines 75+ years of hands-on product development experience with a hybrid approach utilizing classical and modern methodologies to accelerate development timelines and reduce costs.

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_Profile last updated: 2026-10-13T07:03:22.144Z. Profile facts may include AI-assisted enrichment._

Auto-generated by BioBM Editorial AI for machine-readable profile access.