High-quality, audit-ready Clinical Data delivered seamlessly with our Data Management Services
At Navitas Life Sciences we pride ourselves on the seamless delivery of high-quality audit-ready clinical data documentation. Through quarterly reviews, comprehensive personnel training, and regular currency updates, we ensure you data remains reliable and effective. High-quality data enhances the efficiency and effectiveness of clinical trials, leading to better decision-making and successful outcomes.
Our experts play a crucial role in the success of your data management solutions, enabling you to present the results from your clinical trials effectively. Trustworthy data is essential for making informed decisions and driving your clinical trials forward.
Delivering comprehensive and flexible Data Management Support
- Database & eCRF Design, Edit Checks, Programmed Dynamics, & User Acceptance Testing (UAT)
- EDC Platform Development: InForm, Medidata RAVE, Veeva Vault, Medrio, & OpenClinica
- Programmed Standard & Smart Data Listings
- Data Quality, Data Cleaning, & Query Resolution
- Serious Adverse Event (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
We are your one-stop shop for all data management needs. We pride ourselves on delivering clean, high-quality data and offer complete support or augmentation of your existing team. Our expert team of Clinical Data Managers collaborate closely with your Medical and Clinical teams to:
- Build out a database within specified deadlines
- Develop a protocol from scratch and get the database up and running
- Quickly turn over deliverables when a new protocol is presented
- Provide 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 you are audit-ready and able to demonstrate the steps taken to arrive at your data
- Write DMP, CCG, DVS, Coding Guidelines, or RD
Brochure
A Global FSP helping you to meet the challenges of data requirements in clinical trials
BLOGS
Navitas Data Sciences’ Cutting Edge Clinical Data Science for Efficient Clinical Trials
Navitas Data Sciences and PHUSE: Collaborating for Innovative Solutions in Data Science in Clinical Trials
