Data
Management

High-quality audit-ready clinical data
delivered seamlessly

HIGH QUALITY AUDIT-READY DATA DELIVERED BY EXPERTS

Seamlessly delivering high-quality audit-ready clinical data documentation with quarterly reviews, personnel training, and currency reviews. The quality of data improves the efficiency and effectiveness of clinical trials and leads to better decision-making.

Data that is Reliable is Data that you can use

Our experts contribute to the success of your Data Management solution, enabling you to present the results from your clinical trials effectively.

Flexible and Industry Leading Data Management Support

  • Database & eCRF Design, Edit Checks, Programmed Dynamics, & UAT
  • EDC Platform Development: InForm, Medidata RAVE, Veeva Vault, Medrio, & OpenClinica
  • Programmed Standard & Smart Data Listings
  • Data Quality, Data Cleaning, & Query Resolution
  • SAE Reconciliation/External Data Reconciliation
  • External Vendor & Project Team Management
  • Document Creation including DVS, DMP & Data Entry Guidelines
  • Audit Readiness & Study Documentation Management

Count On US TO DELIVER AUDIT-READY TRUSTWORTHY DATA

Navitas Data Sciences is your one stop shop for all data management needs. We pride ourselves on the quality and cleanliness of the data that we deliver and can provide you with complete support or augment your existing team. We understand the different complexities of work and our expert team of Clinical Data Managers will work with your Medical and Clinical teams to:

  • Build out a database within specified deadlines
  • Take a protocol from scratch and get the database up and running
  • Quickly turn over deliverables when a new facing protocol is presented
  • Provide a proper interpretation of the protocol
  • Support the migration of your database regardless of complexity
  • Meet study start-up dates and follow go-live timetables
  • Ensure that you are audit-ready and able to demonstrate the steps you took to arrive at the data you have
  • Write DMP, CCG, DVS, Coding Guidelines, or RD

Meet the challenges of data requirements in your clinical trials with our flexible global FSP

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