Clinical trials

We are a full-service Contract Research Organization (CRO) that conducts and manages ethical clinical research on drugs, biologics, medical devices and natural health products. We have the quality service and legal access to regulatory authorities in the EMEA Region. Our services extend to cover the needs of pharmaceutical, medical device, or biotechnology industries. We can meet your needs, whether your goal is for pharmacovigilance, drug development and discovery, submission-ready datasets, or any other goal of your organization's desire. This includes numerous specialized services that support the Medical development and clinical trials process.

Including...

  • Clinical Protocol Development
  • Regulatory & Ethical affairs support & Submissions
  • Case Report Form Design
  • Electronic Data Capture (EDC) System
  • Investigator Identification
  • Client - tailored training
  • Study Site Identification and Qualification
  • Investigator Education
  • Study Site Management
  • Clinical, Medical and Safety Monitoring
  • Data Management & Statistical Analysis
  • Medical Writing
  • Evaluation of reports
  • Medical writing services
  • Auditing and Quality Assurance
EMEACR is a leading bio/pharmaceutical services organization that strives to empower product development through designing and developing highly reliable medical development services for mission-critical products and applications. We provide high quality deliverables and exceptional services within impressive timelines on every project we manage.