Our Clinical Expertise

Clinical solutions tailored for your specific needs.

Therapeutic Expertise

Our team possesses deep knowledge in the musculoskeletal field.
Whether you’re developing a supplement, a drug or a medical device, we have the expertise to guide you through the regulatory requirements and clinical trial considerations.

Product Expertise

We understand the unique challenges associated with developing different types of products. Our team has extensive experience working with medical device, drug and food supplements. We can tailor our approach to ensure your clinical trials effectively evaluate the safety and efficacy of your specific product.

Type of Studies

Artialis offers a comprehensive range of clinical trial designs, from Phase I First-in-Human studies to Phase IV post-marketing surveillance. We’ll work closely with you to determine the most appropriate study type to meet your development goals and regulatory requirements.

  • Early phase, FI and Phase 1 on drug
  • Phase II on drug
  • Phase IV post market on drug
  • Pre-market and post market studies on MD
  • Food supplement studies
  • FIH and post market studies
  • Veterinarian studies
  • Satisfaction survey
  • Usability studies

Regulatory

Navigating the complex regulatory landscape is crucial for successful clinical trial execution. Our team possesses a deep understanding of global EU regulatory requirements. We’ll guide you through the entire regulatory process, ensuring your clinical trial program meets all necessary standards.

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Receive the latest on industry insights & Artialis news.