Search CROs

• Biologics (Monoclonal Antibodies)

Boutique biologics CDMO providing analytical method development, process development, and cGMP manufacturing for biotech clients from early research through Phase 3, backed by over 20 years of experience and state-of-the-art facilities.

Anthea Pharma is an injectable CDMO in Hyderabad, India, offering development and manufacturing of vials, emulsions, lyophilized vials, and prefilled syringes. The company highlights aseptic fill and finish, terminal sterilization, lyophilization, and formulation and analytical development for clients.

• Medicinal Chemistry
• Small Molecule

HAARES ChemTech provides custom synthesis and contract R&D for complex organic molecules from Edmonton, Canada. Its PhD-level chemists work from milligram to multi-kilogram scale, and the company also offers process development and intermediate manufacture.

• Clinical Operations
• Clinical Trial Services

Care Access runs health screenings and connects volunteers to clinical trials, with site support staffing and referral services for research sites. It operates through country sites in the U.S., Canada, Poland, and Brazil.

• Bioanalysis
• Biostatistics & Statistical Programming
• Central Laboratory Services

ICBio is a Bengaluru-based CRO offering bioavailability/bioequivalence studies, phase II–IV clinical trials, and LC-MS/MS bioanalysis. The excerpts cite regulatory approvals from DCGI-CDSCO, ANVISA, and EMA.

• Analytical Method Development & Validation
• Discovery Research
• Medicinal Chemistry

Sapala Organics is a nucleic acid chemistry CRO and CDMO offering custom synthesis of oligonucleotide building blocks, oligo-based drug development and manufacturing, and orthogonal analytical services. The company is now a subsidiary of Cohance Lifesciences.

• Bioanalysis
• LC-MS Bioanalysis (Small Molecule)
• Antibody-Drug Conjugate (ADC)

Bioanalytical CRO delivering LC-MS/MS bioanalysis for small molecules, peptides, proteins, and ADCs, with method development and PK/TK support. The company reports 5-business-day study initiation and 98% on-time data delivery.

• Clinical Operations
• Phase I Clinical Trials
• Phase II Clinical Trials

ProRelix Research supports Phase 1–4 clinical trials across pharmaceutical, biotechnology, and medical device sectors, offering clinical trial project management, data management, and medical writing services in compliance with ICH and GCP principles across the US, India, Europe, and Australia.

• Biostatistics & Statistical Programming
• Clinical Operations
• Phase I Clinical Trials

Data-focused CRO providing full-spectrum biometrics, regulatory submissions, safety & risk management, and therapeutic expertise across oncology, CNS, rare diseases, and psychedelics. Named Best Specialist CRO at the Scrip Awards with zero refusals to file on 50+ marketing applications in five years.

• Computational & In-Silico Drug Discovery
• Discovery Research
• GLP Toxicology

ChemDiv is a fully integrated target-to-clinic CRO headquartered in San Diego, CA, offering drug discovery services including medicinal chemistry, CADD, ADME/DMPK, toxicology, and custom synthesis alongside the industry's largest commercial screening library of 1.6M compounds.

Japanese chemical manufacturer organized into four business segments: agro and life solutions, ICT and mobility solutions, advanced medical solutions, and essential and green materials. Its site lists R&D laboratories and product search, but the excerpts show no third-party contract development or manufacturing offering.

• Biostatistics & Statistical Programming
• Clinical Operations
• Data Management & eClinical

Biometric CRO delivering clinical data management, biostatistics, statistical programming (SDTM/ADaM), and medical writing for biotech, pharma, and medtech sponsors. Offers a functional service provider model and the BioGRID trial analytics platform.

• Bioanalysis
• Biomarker Assays
• Biostatistics & Statistical Programming

Amador Bioscience provides bioanalysis and biomarker services, including LCMS, immunoassays, flow cytometry, and immunogenicity testing, alongside clinical pharmacology modeling and regulatory affairs support. Its labs are GLP compliant, and its teams work across the US, China, and Europe.