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Clinical Research Services, from Start-Up to Submission

Seven service areas for sponsors, CROs, SMOs, hospitals, research sites and healthcare start-ups, delivered by a remote-first team that works across India.

Regulatory Writing, Site Start-Up & CTA Contracting

Documents, approvals and agreements in place so studies reach first-patient-in faster.

  • Drafting, reviewing and negotiating CTAs, MSAs and CDAs
  • Protocol amendments, ethics committee submissions and CTRI documentation
  • Start-up milestone tracking, investigator budgets and turnaround optimisation
  • eTMF set-up and operational metric tracking
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Site Management (SMO) & Site Operations

GCP-ready sites that recruit well, document cleanly and stay inspection-ready.

  • Feasibility assessments, site selection dossiers and investigator meetings
  • Participant recruitment and retention plans, and informed-consent workflows
  • Source data verification support
  • Audit-ready TMF/ISF oversight and GCP compliance monitoring
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Clinical Data Management

Reliable trial data from first entry to database lock.

  • eCRF design, data validation specifications and edit-check programming
  • Medical coding with MedDRA and WHO-DD
  • Query generation, discrepancy management and database lock
  • CDISC-aligned data handling and ALCOA+ data integrity
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Biostatistics & Data Analytics

Analysis that is accurate, transparent and ready for review or publication.

  • Sample size calculation and statistical analysis plans
  • Descriptive and inferential statistics and modelling
  • Systematic reviews and meta-analyses following PRISMA (pairwise and network)
  • Analysis in SPSS, GraphPad Prism, R, Python and Base SAS
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Drug Information, Pharmacovigilance & Medical Writing

Accurate information and timely safety reporting that protect patients.

  • ICSR processing, safety narratives and MedDRA adverse-event triage
  • Medical inquiry handling and evidence-based drug information
  • Product monographs and investigator brochures
  • Clinical study reports (ICH E3) and manuscripts
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Clinical Research Branding & Marketing

A credible, scientifically accurate brand that wins sponsors, partners and participants.

  • Brand strategy and identity for CROs, SMOs, research sites, hospitals and pharma start-ups
  • Capability decks, company profiles, brochures and site profiles for sponsor feasibility
  • Website copy, articles, case studies and LinkedIn marketing
  • Conference, CME and webinar collateral
  • Participant awareness material, prepared for ethics committee review

Business Development & Partnership Consulting

A data-backed plan to find sponsors, build partnerships and grow.

  • Market research and feasibility for new clinical research and healthcare ventures
  • Sponsor and CRO outreach strategy, proposals and RFP responses
  • Hospital–SMO alliances, CRO collaborations and college–industry MoUs
  • Business plans, go-to-market strategy and KPI reviews
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How an Engagement Works

  1. Discovery Call

    We understand your study, timelines and constraints.

  2. Proposal

    A clear scope, team, timeline and quote.

  3. Kick-Off

    Named contacts, a communication plan and agreed SOPs.

  4. Delivery & Reporting

    Regular status updates and quality-checked deliverables.

Have a Study or Project in Mind?

Call our partnerships desk on +91 97650 06083, or send an inquiry and we will set up a discovery call.

WhatsApp us