Clinical Data Analytics
Clinical Data Analytics

Our Capabilities
Hayagriva Multinational Technologies provides flexible and scalable engagement models to manage your Biostatistics and SAS Programming staffing and outsourcing needs. These models assure quality services, constant communication, improved efficiencies and up to 15% – 40% cost savings. We offer wide range of expertise in all phases of clinical trials (I-IV), with pool of expert statisticians and statistical programmers holding advanced degrees and having a strong exposure to various therapeutic areas. Our team works with the end goal in mind, which is the timely submission of results from various clinical stages in order to support regulatory review, approval and monitoring of patient safety.
SAS Programming:
- Standardized approach for analysis files
- Transportable tools to support standard non-efficacy reports
- Programming for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)
- Programming of tables/listings/figures for clinical study report and data monitoring committee
- Programming based on analysis data
- Independent quality reviews
- Customized clinical data outputs
- Proactive, results-oriented approach to programming
- Preparation of Case Report Tabulations (CRT) for submission
- Programming based on data validation plan
CDISC Services
- Ensure accurate interpretation of the Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM)
- Convert datasets from legacy studies to SDTM
- Annotate Case Report Forms (CRFs) as per SDTM standards
- Create dataset specifications for ADaM datasets
- Create mapping specification for SDTM domains
Biostatistics
- Consultation on study design
- Protocol development
- Randomization
- Statistical Analysis Plan (SAP)
- Sample size calculations
- Interim analysis
- DSMB participation
Let’s Connect
At Hayagriva Multinational Technologies, we’re here to address your IT needs with tailored solutions and expert support. Reach out to us today!