CRO Finder

Pain CROs

Contract research organizations with pain expertise

19 organizations found

Axis Clinicals

Dilworth, MN, USA Specialty

Clinical pharmacology and bioanalytical CRO providing Phase I studies, bioequivalence, and PK/PD studies from a purpose-built 150-bed clinical pharmacology unit in Dilworth, Minnesota.

GCP Compliant GLP FDA Registered

Basi Research (CROS NT)

Milan, Italy Specialty

Italian CRO providing Phase I clinical pharmacology studies including bioequivalence, food-effect, and drug interaction trials from its dedicated Phase I unit in Milan.

GCP Compliant GLP

Biotrial

Rennes, France Specialty

Transatlantic Phase 1 CRO with clinical pharmacology units in Rennes (France) and Newark (NJ, USA). Specializes in first-in-human, CNS, cardiac safety, and abuse liability studies.

GLP GCP Compliant ANSM Approved

CHDR

Leiden, Netherlands Specialty

Independent early-phase CRO in the Netherlands specializing in first-in-human and Phase I trials using innovative biomarkers, with a purpose-built 54-bed clinical research unit adjacent to Leiden University Medical Center.

GCP Compliant ISO 9001

Clinical Ink

Winston-Salem, NC, USA Specialty

Clinical technology company providing eCOA, eConsent, and clinical data capture solutions integrated with CRO-like trial management capabilities for decentralized and hybrid clinical trials.

GCP Compliant ISO 27001

Clinilabs Drug Development

Eatontown, NJ, USA Specialty

The only global full-service CRO focused exclusively on CNS drug development, with involvement in 22 FDA-approved CNS therapies across 13 indications.

GCP Compliant GLP FDA Registered

Eurofins Panlabs Discovery

Toulouse, France Testing Lab

Eurofins Discovery division providing high-throughput in-vitro pharmacology screening, compound profiling, ADME assays, and bioanalytical services supporting drug discovery from target identification through lead optimization.

GLP ISO 9001 ISO 17025

Haskell Clinical Research

Manalapan, NJ, USA Specialty

Phase I clinical research unit in New Jersey providing first-in-human, food effect, bioequivalence, and early-phase pharmacokinetic studies for pharmaceutical sponsors.

GCP Compliant FDA Registered

Jubilant Biosys

Bangalore, India Full Service

Integrated drug discovery and development services company providing medicinal chemistry, ADME/DMPK, pharmacology, and clinical research from India, US, and China operations.

GLP GMP ISO 9001

MedPharm US

Durham, NC, USA CDMO

Specialist topical and transdermal formulation development CRO and CDMO offering dermal PK, in vitro permeation, bioequivalence, and formulation development services.

GMP GLP FDA Registered ISO 9001

Oakwood Labs

Oakwood Village, OH, USA CDMO

Specialized CDMO focused exclusively on sustained-release long-acting injectable formulation development, aseptic fill-finish, and lyophilization.

GMP FDA Registered

Pharma Solutions Group

Montreal, Canada Full Service

Canadian full-service CRO providing clinical research services from Phase I through Phase IV with particular expertise in bioequivalence studies and pharmacokinetic trials.

GCP Compliant GLP

PharmaEngine

Taipei, Taiwan Specialty

Taipei-based drug development company and CRO specializing in oncology, running Phase I-III clinical trials for new cancer therapies and out-licensing proprietary pipeline assets.

GCP Compliant

Pinnacle Biomedical Research

Phoenix, AZ, USA Specialty

Clinical research site in Phoenix conducting Phase I-IV clinical trials with particular strength in CNS, pain, and metabolic disease studies with rapid enrollment capabilities.

GCP Compliant

Prism Clinical Research

Saint Paul, MN, USA Specialty

Multi-site clinical research organization conducting Phase I-IV trials with a network of dedicated research sites across the upper Midwest specializing in diverse therapeutic areas.

GCP Compliant

Quotient Sciences (US)

Miami, FL, USA CDMO

Translational pharmaceutics CRO/CDMO uniquely combining formulation development and clinical pharmacology under one roof, accelerating drug development timelines by running formulation and clinical testing simultaneously.

GMP GCP Compliant GLP FDA Registered

Richmond Pharmacology

London, UK Specialty

London-based Phase 1 clinical research unit specializing in early phase clinical trials, pharmacokinetics, and healthy volunteer studies. Located at Guy's Hospital campus.

GCP Compliant MHRA Approved

Spaulding Clinical Research

West Bend, WI, USA Specialty

US-based early phase CRO specializing in cardiac safety (thorough QT/QTc) studies, abuse deterrent formulation, and human abuse liability studies. Operates a 120-bed clinical facility.

GCP Compliant FDA Registered

Veeda Clinical Research

Ahmedabad, India Specialty

Indian CRO providing Phase I clinical pharmacology, bioanalytical services, and bioequivalence studies from a 230-bed clinical pharmacology unit in Ahmedabad with USFDA and EMA track record.

GCP Compliant GLP ISO 9001