Quality Services in Clinical Research
We are a leading provider of quality services and resources in Clinical Data Management, Clinical SAS, Clinical Biostatistics, CDISC Submissions, Regulatory, Medical Writing, and more. Join us for excellence in Clinical Operations globally.
Our Services
Biostatistics and SAS Programming
The role of statistical programmers is to use their superior technical and programming skills in order to allow clinical trial statisticians to perform their statistical analysis duties more efficiently. Statistical analysis and programming for clinical research.
Clinical Data Management
Efficiently manage and analyze clinical trial data. The Study Data Tabulation Model (SDTM) and associated Implementation Guides are intended to guide the organization, structure, and format of standard human, animal and medical device trial tabulation datasets.
Drug Safety Services
Pharmacovigilance or Drug Saftey is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.Ensure drug safety compliance and reporting.
Clinical Operations
Clinical operations manager provides timely and accurate guidance to affiliate Clinical staff on the effective implementation of ICH GCP, existing or revised global and local Controlled Documents, regulatory and local law requirements.
Regulatory Support
We specialize in offering regulatory and compliance services in India. Navigating the intricate path from the inception of a concept to product approval can be challenging, particularly in light of rigorous regulations.
Medical Writing
medical writers are detailing, documenting, and sharing news and research that is improving health outcomes and saving lives.