The regulatory division in our company offers a wide range of regulatory services to our clients that covers:

   Global regulatory consultancy/submissions
   Obtaining approvals from authorities forclinical trials
   Registration dossier submissions and follow up,
   Pharmacovigilance and import/export license for drugs, IMPs
   Bio-samples and other study materials

  Project Management

  Study Monitoring

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Biological and IMP Logistics

  Quality Assurance



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