Agati specializes in standardization of clinical trials data in compliance with CDISC data standards or sponsor defined standards. With our metadata driven standardization approach our customers are guaranteed to receive quality deliverables in the shortest possible time with significant cost savings.
- Conversion of the on-going or legacy trial data into CDISC SDTM data standards
- Conversion of analysis data as per CDISC ADAM data standards
- Define.xml creation/ validation services as per Define.xml 1.0 and 2.0 specifications
- CRF Annotation and Reviewer’s guide development
- Edit check Programming and Validation
- Laboratory/Vendor Data Reconciliation
- Safety Data Management and Reconciliation
- On-shore and Off-shore Clinical Data Management services
The Agati Advantages
- Our delivery models offer upto 40% cost efficiency.
- Flexibility to adhere either to the Client SOP or Internal SOP.
- Robust data security and quality management practises
- Strong bench strength that helps scale to varying work loads