Why Cytespace

100+

Years in Project Management

150+

Clinical Trials

35+

Clients

25+

Cities

200+

Sites

35

years in Neurology & Psychiatry

40

years in Cardiovascular & Metabolism

25

years in
Vaccination

25

years in Respiratory and Gastroenterology

30

years in Infectious Diaseases & Immunology

60

years in
Oncology

20

years in Medical Device & Medical Affairs

End to End Solutions

  • eCRF Design, edit check, Data Coding and validation for large complex Phase III studies in less than 6-8 weeks compare to industry standard of 12-14 weeks.
  • Lean Back end check design, program and reviews process - Data review time reduces significantly by 20%
  • Database lock in less than 21 days from LPV

Deliverables

  • Effective Quality Control steps and documentation
  • Risk Analysis
    and mitigation plans
  • Expertise and experience in CDISC deliverables including Define.xml - starts right from eCRF design phase until Data submission.