Question 1

What are the key benefits of using ShareCRF for my clinical trial?

Accepted Answer

ShareCRF significantly reduces study setup time, eliminates the need for coding expertise, ensures data compliance with regulatory standards, and provides a flexible platform adaptable to various study designs, ultimately accelerating your research and reducing costs.

Question 2

Is ShareCRF compliant with industry regulations like 21 CFR Part 11?

Accepted Answer

Yes, ShareCRF is designed and validated to support compliance with key industry regulations, including 21 CFR Part 11, ensuring data integrity, audit trails, and electronic signatures are properly managed.

Question 3

What level of technical expertise is required to use ShareCRF?

Accepted Answer

ShareCRF is designed for ease of use and requires no coding skills. Its intuitive interface allows researchers and study managers to configure and manage studies independently.

Question 4

Can ShareCRF integrate with other clinical research tools?

Accepted Answer

ShareCRF offers integration capabilities with various clinical research tools and systems, allowing for seamless data exchange and workflow optimization. Specific integrations vary, so please contact us for details.

Question 5

How does ShareCRF handle data security and privacy?

Accepted Answer

Data security is a top priority. ShareCRF employs robust security measures, including data encryption, access controls, and regular security audits, to protect patient data and maintain privacy.

Question 6

What kind of support and training does ShareCRF offer?

Accepted Answer

We provide comprehensive support, including detailed documentation, online tutorials, and dedicated customer support via email and phone. Training options are also available to help you maximize the platform's capabilities.

Question 7

Is ShareCRF suitable for both small and large clinical trials?

Accepted Answer

Yes, ShareCRF is scalable and adaptable, making it suitable for clinical trials of all sizes and complexities, from small investigator-initiated studies to large, multi-site trials.

Question 8

What types of data can be captured using ShareCRF?

Accepted Answer

ShareCRF can capture a wide range of clinical trial data, including demographic information, medical history, adverse events, laboratory results, and patient-reported outcomes (PROs). It supports various data types and validation rules.

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