We offer comprehensive services including Phase I-III clinical trials, feasibility studies, medical writing, project management, site management, data management and statistics. To meet the requirements of our clients, we offer clinical trial services in India and USA. We have our own teams in India and we operate through strategic relationships with partner CROs in the other regions.

We have highly experienced and qualified functional teams to conduct Clinical Trials, from the study design to commercialization. Our expert team helps you design the study, select endpoints, and advise on sample size calculation strategies/justifications for reducing the sample size without compromising endpoints and study results. Our operations team ensures start-to-end trial management, patient | subjects recruitment and retention strategies, timelines, budget, quality & compliance.

  • Feasibility Check
  • Study Design – Scientifically substantiated claims | therapeutic claims
  • Sample size calculation
  • Investigator(s)/Site Selection
  • KOLs (Key Opinion Leaders) Identification
  • Clinical Safety & Monitoring
  • Data Management
  • Full-Scale Statistical Analysis
  • Clinical Study Report
  • Manuscript Writing |Journal Publication
  • Medical Overview of the clinical trials
  • Training of Study Teams and sites
  • Review or audit medical records for completeness and accuracy.
  • Often coordinate in-service meetings to educate the medical staff on proper documenting procedures.
  • Continue self-learning of new coding, government, and insurance guidelines.
  • Quality Control check for complete, legible documentation.
  • Review comments within projected timelines.

NeighbourCare offers comprehensive clinical trial monitoring and site management services from feasibility through site closeout to support clinical trials worldwide. Our clinical services are tailored to your needs. All monitoring activities follow the study protocol, clinical monitoring plan, Standard Operating Procedures, ICH-GCP, and applicable regional regulations. Qualified, knowledgeable professionals provide our clinical trial monitoring and site management services with extensive clinical research and therapeutic area experience.

  • Site Identification & Selection
  • Site feasibility assessments
  • Site Qualification & Initiation
  • Budget and Contract Negotiations with Sites
  • Ongoing site monitoring & management
  • Regulatory document collection, review & management
  • Management/facilitation of IRB/EC submissions
  • Remote monitoring via EDC
  • 100%, Targeted or Risk Based on monitoring
  • Electronic Trial Master File management (eTMF)
Medical writers are critical to the communication process of outlining the goals, strategies, analysis, and medical understanding of a clinical trial/program to patients, sites, sponsors, and regulatory agencies. Our scientific-minded writing team has significant experience preparing clinical documents, including Protocols, informed consent documents | and Clinical Study Reports (CSRs). We understand the complexities of writing in a highly regulated environment and the challenges of varied requirements of different regulatory agencies.
  • Protocol Synopsis, Protocols, and Amendments
  • Informed Consent Forms | Assent forms | Parental Consent
  • Clinical Study Reports (CSRs)
  • Subject Diaries
  • Case Report Forms (CRFs)
  • Clinical Study Recruitment Package | Advertisements