ParadigmIT Technology Services is a global technology solutions provider focused on delivering customer value through high-quality processes and cost-efficient solutions. Paradigm has been one of the trendsetters in global delivery practices with our Client-Centric Model for customer management and delivery. Established in 1998, Paradigm has global clientele in Fortune 500 and Government Sectors. Our teams provide the entire range of IT solutions from strategy consulting to implementation and maintenance across a range of sectors.
ParadigmIT offers a host of services for pharmaceutical, biotech, medical devices, Universities, and life science companies including a host of Clinical Research applications. They provide customized, end-to-end Clinical Data Management Services as per customer needs. ParadigmIT team consists of functional, technical and industry experts, who can successfully assist pharma, Bio and life sciences companies in navigating the complexity of the clinical trial lifecycle. The combined expertise consulting can be leveraged to identify the best suitable and pocket-friendly Clinical Operational and Clinical Data Management technologies from the market. ParadigmIT Streamlines your Clinical Trial Process, empowering the whole ecosystem, and bringing new therapies to patients, faster with great quality, while staying compliant with regulations.
Providing solutions across your Clinical Study experience with high quality deliverables and better return for your investment. They have successfully completed 1500+ EDC setup, worked with 43+ Sponsors/CRO, 10K Projects in clinical Trial, and had User Administration support from their team.
“Clinical Trial Data Combined With Advanced Business Intelligence Technology Will Benefit Our Customer To Save Cost And Time.”
Organized Service Offering
ParadigmIT has assessed multiple systems and understands the best-in-class applications/tools for your Clinical Trials. We take all your worries to bring in apt technology solutions per the trial design requirements. Our focus is to get
- The trial kick off on time
- Standardized eCRFs development is ready to map into respective SDTM domains
- Collect unambiguous and quality data from sites
- Timely receipt of external vendor/third party data
- Frequent review of Safety and Protocol end points data via BI tools
- Insight generation to Clinical Operations and CDM team on foresighted risks
- Custom solutions to handle the live integrated data of eCOA/ePRO
- Clinical Data Management
- Project Management
- Clinical Trial Management
- Regulatory affairs
- Biostatistics
- Site Selection and start-up
- Medical Writing
- Quality Management and Training
About Clinical Trials Innovation Programme 2023
Clinical Trials Innovation Programme is an invitation-only, premium event bringing together a mix of clinical research professionals and service providers in one stimulating environment.
Join us face to face to learn from the best in the drug development industry and have an opportunity to learn from their experiences. With an agenda covering the future of Clinical trials and drug development post COVID, Clinical Trials Innovation Programme 2023 will feature tailored sessions presented by the leading experts from across the globe.
We are bringing together the best in the industry to help you learn and grow, and accelerate your drug development journey. The experts will include thought leaders and visionaries from Danish Medicines Agency, Bayer Pharmaceuticals, AstraZeneca The Janssen Pharmaceutical Companies of Johnson & Johnson, Travere Therapeutics, Biogen, Vifor Pharma, Medical Products Agency and much more.