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Clinical Trials – Protocol Development

Clinical Trials – Protocol Development

Your clinical investigation cannot begin without a clinical protocol development. Pacific Link Consulting has many years of experience developing clinical trial protocols for many different compound types. By utilizing our skilled in-house consultants and partners, Pacific-Link Consulting can thoroughly and efficiently develop a protocol to meet your clinical investigation needs. Our consultants and our partners are on hand for all your protocol needs.

PLC can assist your protocol development with:

  • Study Design Consultation
  • Research protocol
  • Interventional
  • Multi-site
  • Single site
  • Greater than Minimal Risk studies
  • Different data types
  • Data handling
  • Data analysis
  • Record keeping
  • Monitoring and reporting
  • Outcome measures
  • QC and QA
  • Financing and Insurance
  • Statistical methods and analysis
  • Termination criteria

The above list is not a comprehensive overview of our services. Please contact us to learn more about how we can assist you.

Other Clinical Trial Services

Pacific Link Consulting can file Clinical Trial Applications (CTAs) in Canada on a clients’ behalf. We can help the client obtain legal authorized representative for the region, project manage your CTA, write and prepare meeting requests as well as meeting packages.

Pacific Link can also assist the client with clinical trial data management, clinical trial monitoring and clinical protocol development.

Other markets of expertise include Japan and Europe.

Please contact us to learn more about what Pacific-Link Consulting can do for your project.

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