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Katalyst CRO

Québec, Québec

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À propos de Katalyst CRO

Trusted Business Partner

Secteur
Business Consulting and Services
Taille de l’entreprise
51 à 200 employés
Siège social
South Plainfield, NJ
Type d’entreprise
Entreprise privée

Présentation originale de l’entreprise

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!

Spécialités

  • 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

Établissements

  • 285 Durham Ave, Suite 12, South Plainfield, NJ 07080, US

  • 285 Durham Ave, Suite 12, South Plainfield, New Jersey 07080, US

Les emplacements du profil de l’entreprise peuvent être hors de cette zone. Ils ne recrutent pas tous.

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Abonnés
24 781
Personnes liées à cette entreprise
137

Personnes qui indiquent cette entreprise sur LinkedIn. Il ne s’agit pas d’un effectif vérifié. Les chiffres proviennent du profil enregistré.

Catégorie d’employeur

Autre employeur

Catégorie estimée à partir du profil de l’entreprise, sans confirmation de l’employeur.