The regulatory division in our company offers a wide range of regulatory services to our clients that cover 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 Writing

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Data Management & Statistics

  Biological and IMP Logistics

  Quality Assurance