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Data on a Touch Pad

Data Management

Services​

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At R-S-S, our comprehensive Clinical Data Management (CDM) services are designed to ensure the accurate collection, validation, and analysis of clinical trial data. With a focus on quality and compliance, we streamline the management of clinical data to support informed decision-making and accelerate the development of lifesaving treatments. Our commitment to data integrity and regulatory compliance ensures that your clinical trial data is managed efficiently, allowing for faster, data-driven decisions.

Why Choose Us?

Expertise in Global Regulatory Compliance: We adhere to international standards such as CDISC, ICH, GCP, and FDA guidelines.

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Cutting-Edge Technology: Implementing innovative EDC platforms and data management solutions to streamline the trial process.

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Dedicated Team of Experts: Our experienced clinical data managers, biostatisticians, and IT professionals ensure smooth and efficient study data management.

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Data Security and Confidentiality: We prioritize the security of your sensitive clinical data, ensuring that it is protected throughout the trial process.
 

Illuminated Abstract Shapes

Our Expertise in Data Management

CRF Annotation

Electronic Case Report Form Designing
(eCRF)

Data Extraction

Data Entry & Validation

CDISC Compliance

Randomisation

Database Development, Validation & Testing

Medical Coding

ePRO & eCOA

Clinical Data Review & Query Management

Data Management Plan

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