About Katalyst CRO
Trusted Business Partner
- Industry
- Business Consulting and Services
- Company size
- 51-200 employees
- Headquarters
- South Plainfield, NJ
- Company type
- Privately Held
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions
Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide.
With a strong foundation in cGxP & ICH-GCP-compliant clinical research, we offer fully customizable, end-to-end solutions, covering everything from pre-clinical studies to Phase I–IV clinical trials, regulatory affairs, and validation services - ensuring seamless drug and device development.
Our Expertise Across the Product Lifecycle: 🔹 Pre-Clinical Research & Development – In-Vitro (Lab-Based) & In-Vivo (Animal) Studies 🔹 Clinical Research & Development – Trial Management, Data Management, Biostatistics, Medical Writing, Pharmacovigilance 🔹 Regulatory & Quality Compliance – cGxP (GMP, GLP, GCP) Validations, Regulatory Affairs, Process & System Validations 🔹 Strategic Human Resourcing – Connecting top-tier talent to life sciences and healthcare organizations
With deep industry expertise and a flexible, client-centric approach, Katalyst CRO leverages an advise-build-operate model to de-risk and accelerate research programs. We help organizations achieve regulatory success, optimize quality systems, and bring life-changing therapies to market faster - ultimately improving global patient health and safety.
💡 Partner with Katalyst CRO to bring breakthrough therapies to market with confidence.
📩 Let’s connect and shape the future of healthcare together!
Specialties
- Clinical Research
- Clinical Trials
- Clinical Trial Operations
- Clinical Trial Monitoring
- Clinical Data Management
- Clinical Statistical Analysis
- Pharmacovigilance/Drug Safety
- Quality Control & Compliance
- Regulatory & Intellectual Property
- Validations
- Pharmaceuticals
- Medical Writing
- Regulatory Publishing & Submissions
- Pharma Software Implementations
- Pharma/Clinical Staffing
- Pharma/Clinical Consulting
- and HEOR
Company locations
285 Durham Ave, Suite 12, South Plainfield, NJ 07080, US
285 Durham Ave, Suite 12, South Plainfield, New Jersey 07080, US
Locations listed on the company profile. These may include offices outside Canada, and not every location is hiring.
On LinkedIn
- Followers
- 24,781
- People linked to this company
- 137
People who list this company on LinkedIn, not a verified employee count. Figures reflect the saved company profile.
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Employer category
Other employer
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