Israel & Middle East Services and Experience

While there has been an increase in clinical trials conducted in these regions in recent years, companies that provide support need to make changes in their business models and growth strategy to align themselves with the huge opportunities that lie ahead.

As a global dCRO, we recognize the expertise and local knowledge of clinical investigators, patient populations, regional regulatory nuances and cultural differences required to successfully run trials in these areas.

We are headquartered in Research Triangle Park, NC, USA, with Middle East offices in Tel Aviv, Israel. Within these offices we deliver a full array of outsourced regulatory, strategic development, clinical development, and post-approval services.

 

 

  • Biostatistics
  • Clinical Monitoring
  • Data Management
  • GCP training
  • Global Study Feasibility
  • GxP/CMC Quality Assurance Consultancy
  • Legal Representation
  • Patient Recruitment
  • Pharmacovigilance & Safety surveillance
  • Project Management
  • Regulatory & Strategic Consultancy
  • Regulatory Submissions & Filings
  • Site Selection & Management
  • TEMPO eClinical Platform

 

 

 

  • Oncology: 33%
  • Pulmology: 17%
  • Ophthalmology: 10%
  • Gastroenterology: 7%
  • Hematology: 7%
 

  • Endocrinology: 7%
  • Urology: 3%
  • Infectious Disease: 3%
  • Central Nervous System: 3%
  • Other: 9%

 

 

  • Phase 2: 40%
  • Phase 3: 40%
  • Phase 4: 10%
  • Other: 10%

 

Looking for help in Israel or the Middle East?

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