Specializing in Clinical Data Management, we offer meticulous and comprehensive services for handling, analyzing, and organizing clinical trial data. Our solutions encompass data collection, validation, and database design adhering to regulatory standards. With expertise in EDC platforms, coding dictionaries, and quality control, we ensure accuracy and integrity throughout the data lifecycle. Trust us to streamline clinical trials, facilitating efficient decision-making and regulatory compliance while maintaining the highest standards of data quality and confidentiality.

 

Types:

  • Statistical Input to Protocol/Study Design Development
  • Sample Size Estimation
  • Randomization Schedule
  • Review of CRF and Data Management Plan
  • Statistical Analysis Plan (SAP) and Mock-up Shells
  • Analysis for ISS/ISE/Meta-Analysis
  • CDISC Implementation Service
  • SAS Programming - SDTM/Adam Datasets and Tables, Listings, Figures
  • Data de-identification for regulatory submissions
  • Statistical Report Writing
  • Analysis of Safety, Efficacy Data for CSR and Regulatory submissions
  • Herbal based clinical trials [Ayurvedha and Siddha]
  • Nutraceuticals researches

 

Training

  • Clinical Data Science (any science / engineering graduates)
  • Clinical Data Analyst (any Maths / Statistics / Biostatistics / Public Health / Epidemology students and working professionals
  • Pharmaco Data Science (B Pharm / M Pharm /any Pharmacologist/ PharmacoKinetician / Pharmacometrician and working professionals)
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