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Arkans - Clinical Research Organization

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Welcome To Arkans - Clinical Research Organization

Phase I – III

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Clinical Research Excellence

Strategic approach to phase I – III clinical trials

Arkans offers a full suite of clinical services and functional solutions on a global, regional, and local basis. Our global reach, focused therapeutic experience, client-centric approach, and robust technology are strong pillars supporting your clinical trial success. At these stages, we enlist therapeutic and regulatory experts to build a customized strategy to meet your goals and select the best path forward.

Access to world-class senior medical and clinical advisors, guide the protocol development process and study conduct, adding to the efficiency of our services.



Early Phase I – II and specialized expertise includes:

  • First-in-human and proof-of-concept
  • Micro-dosing
  • Single Ascending Dose/Multiple Ascending Dose (SAD/MAD)
  • Drug-Drug and Food-Drug interaction
  • Flexible trial design, e.g., adaptive, basket/umbrella trial

  • Biosimilarity/Bioequivalence
  • Regulatory affairs strategy, preparation, and submission of CTA/ITA, PIP, IND, PMA/510(k)
  • Pharmacokinetics/Pharmacodynamics (PK/PD)
  • Pet imaging
  • Bioanalytical

  • Pediatric populations
  • Elderly populations
  • Rare disease and orphan indications
  • Medical devices
  • Customer access to executive level oversight with our TFS Governance model

Phase II/III

We provide full-service capabilities for phase II/III trials and pivotal studies for a range of drugs, biologics, and devices, across a large number of therapeutic areas. Each customer receives the same dedication and attention to detail.

  • A dedicated project manager is assigned to each project in agreement with the customer
  • Communication is continuous and transparent
  • A comprehensive project kickoff and planning process is conducted with built-in flexibility to adapt to changes, as needed, throughout your trial
  • Study initiation services and a network of trusted investigator sites for accelerated study start-up are accessible
  • Robust electronic data capture (EDC) systems combined with our clinical trial management system (CTMS) and clinical analytics ensure data integrity throughout your trial
  • A real-time review of EDC metrics is available through our customer portal

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