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Clinical Development

Pharmaceutical Services

Data Management & Biostatistics

Phase III B Programs

Clinical Trial Safety

Medical Affairs

Medical Writing

Quality Assurance

Regulatory Affairs

Pharmacovigilance & Safety Surveillance

Chemistry, Manufacturing, and Controls (CMC) / Quality Assurance

Additional Expertise

Wability delivers the insight and expertise of clinicians, scientists, and experts with competencies that cover every aspect of the drug development process. We take innovative approaches to provide high quality services, within budget, by challenging assumptions about traditional clinical trial design and management.

Our clinical development services include:

  • Revamping clinical development by accelerating pipelines, coordinating both science and technology
  • Partnerships with clinical sites to enhance recruitment rates
  • Engagement with patients to maximize therapeutic efficiency
  • Reduction of cost and implementation of therapeutic insight via innovative strategies
  • Phase II-III studies / Management
  • Site Clinical Monitoring / CRA support
  • Medical Monitoring of Clinical Studies
  • Medical Review of Regulatory Documents
  • Clinical Data Review
  • Clinical Trial Reports
  • Protocol Design and Writing
  • Study Sites Selection and Initiation
  • Investigators Meetings