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Pharmacovigilance & Safety Surveillance

Pharmaceutical Services

Data Management & Biostatistics

Clinical Development

Phase III B Programs

Clinical Trial Safety

Medical Affairs

Medical Writing

Quality Assurance

Regulatory Affairs

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

Additional Expertise

Wability understands that our clients have an enormous responsibility to ensure the safety of those who use their products. Our professionals have vast experience in designing and managing safety surveillance programs. Our project team works with our clients to develop an appropriate trial that identifies and quantifies adverse events (AE), incidents rates and describes the product safety profile. In addition, the teams provide spontaneous AE report collection, processing and regulatory reporting. Each program is customized and can include any or all of the following:

  • Receiving AE reports from healthcare professionals and from customers
  • Triaging calls such as product complaints back to the client side
  • Preparing data for inclusion in periodic safety updates