Clinical Research Services

We are equipped targeting faster patient’s enrollment, minimize protocol/SOP deviations, no/minor Audit observation by highest quality through GxP compliance and detailed monitoring, optimize cost by local FTE cost/services, endpoint monitoring, safeguarding ethical conduct and this assures our sponsor getting reliable results for submission to health authority/publications.

We understand your expectations and earlier pains in Clinical Trials

  • Lower recruitment
  • Protocol & SOP deviations
  • Audit/inspection observations
  • Delayed trials
  • Non-responding CRO/ Sites/ Labs
  • Pending DCFs

 

EXPERTISE

  • Clinical Operations
  • Data Management, Statistics & Programming
  • Regulatory Affairs & Ops.
  • Pharmacovigilance
  • Toxicology
  • Medical Writing
  • Medical Affairs
  • Quality, Risk & Compliance
  • Technology & Solutions
  • CMC & Non-clinical dev.
  • Pharmaco-economics

 

CAPABILITIES

  • >21 years of experience servicing for pharma companies and institutes
  • Associated with Food & Drug Administration
  • >200 Clinical Research Institutes /Hospitals
  • >10 Suppliers
  • Three Offices & One Laboratory
  • Global coverage for all time zones from different geographies
  • Global and regional workforce

 

THERAPEUTIC AREAS

  • Cardiovascular
  • Diabetes and Endocrinology
  • Immuno-Oncology
  • Infectious Diseases
  • Inflammation
  • Neuroscience
  • Non-Alcoholic Steatohepatitis (NASH)
  • Oncology
  • Rare Disease and Orphan Drugs

 

ASSOCIATES

  • Other global network of  CROs at other locations
  • Hospitals/ Institutes
  • Central and peripheral Labs
  • IMP warehouse and suppliers

 

TOOLS/ DATABASE/ANALYTICS

  • Osyscom® Clinical Trial Optimization
  • Osyscom ® Trial Design
  • Osyscom ® Trial Management
  • Osyscom ® Central Monitoring