Real World Clinical Evidence

End-to-End support on evidence generation across hypothesis
building, protocol design, clinical operations, compliance,
biostatistics, medical writing, and publications

Clinical Real World Evidence and Medical Research
enabled through 5000+ centers and 1bn+ clinical parameters

  • Proprietary partners and clinical data collaborations
  • Cutting-edge automation to drive fastest turnaround time
  • Omni-format evidence generation – publications, white papers, medical presentations, multi-media, caselets
  • Extensive coverage – Retrospective, Observational, Prospective, Registries, Case Reports, HEOR, Clinical trial Synthetic arms, among others
  • End-to-end support – hypothesis/ protocol to publication

5000+

partner centers
with data and site
partnerships

5000+

partner centers
with data and site
partnerships

60mn+

unique patient lives
integrated and
managed

60mn+

unique patient lives
integrated and
managed

10+

years longitudinal
data and patient
journeys across
therapy areas

10+

years longitudinal
data and patient
journeys across
therapy areas

25+

therapy areas and
disease conditions
(acute, chronic,
super-specialty and rare diseases)

25+

therapy areas and
disease conditions
(acute, chronic,
super-specialty and rare diseases)

100+

publications and
white papers
across medical
journals and
conferences

100+

publications and
white papers
across medical
journals and
conferences

End-to-end/Full-stack
Research

Hypothesis building and testing to structure effective end points and outcomes

Best-in-class clinical operations, biostatistics, and medical writing teams and processes with 20+ SOPs in-line with the regulatory guidelines and approved by global pharma companies

Collaboration with hospitals, diagnostic labs, practitioners, and independent ethics committees

Identified and Prioritized journals to ensure publication and visibility across right platforms

Tech-enabled Clinical
Operations

eCRF to enable digital data compilation in the
new-age world

Extensive Quality Control backend engine and
workflows to ensure continued data monitoring
and site follow-ups

Detailed Tech and IT SOPs in compliance with the
data, confidentiality, security guidelines

Extensive Compliance
and SOPs

20+ SOPs spanning each micro-step of clinical operations, evidence generation and medical research

SOPs led management of day to day activities of retrospective and prospective studies

Detailed technology and IT SOPs to ensure compliance with local guidelines

Research

Retrospective real world data based clinical studies,
enabled by proprietary clinical data collaborations and
provider partnerships

Observational studies and long-term Registry
programs across a network of 5000+ sites

Phase 4 Clinical Operations, Prospective, and Post
marketing surveillance studies

HEOR hypothesis, modelling and studies

Scientific Content

Proprietary data and evidence backed scientific content and medical communications

Digital-ready and digital-effective scientific communications to enable new-age product commercialization

Trackable micro-sites to enable seamless monitoring of customer interactions and preferences w.r.t. scientific evidence

Surveillance Platforms

Real-time Epidemiology platforms

Infectious Disease Alerts based Surveillance

Decision Support
Algorithms

Risk Assessment – Outpatient and Inpatient

Disease specific risk algorithms

Empirical Treatment Support Platforms

Intervention / Surgical Decision Support

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