Laboratory Information Management System (LIMS) for Clinical Research - Medical / Health Care - Medical Research
Streamline and Automate Clinical Research Workflows Using CloudLIMS - A SaaS, in-the-Cloud Clinical Research LIMS Software. Clinical research plays a vital role in advancing medical knowledge, disease prognosis, and improving patient care. It encompasses the investigation of new drugs, medical devices, and treatments to determine their safety and efficacy. The data generated from clinical research is critical for developing evidence-based guidelines, improving patient outcomes, and informing public health policies.
However, clinical research labs face several challenges, including ensuring the safety and protecting the rights of study participants, complying with ethical guidelines, managing large amounts of data, assuring the quality of results, and recruiting and retaining participants. Clinical researchers must also ensure that their research is conducted in accordance with ICH-GCP guidelines and other relevant standards and regulations to support the validity and reliability of their findings.
CloudLIMS is a scalable, SaaS, in-the-cloud LIMS specifically designed for clinical research labs, CROs, and clinical trials. It supports the data management, automation, and regulatory requirements of your lab, no matter its size or operational complexity. Being in the cloud, CloudLIMS can be accessed anytime, anywhere, is easy to deploy, and enables clinical laboratories to quickly automate without the need to invest in IT infrastructure or personnel, saving time and resources.
- Meet regulatory guidelines and standards such as HIPAA, US FDA, EMEA, CAP, EU GDPR, ICH-GCP, HTA, GCLP, MHRA, and 21 CFR Part 11 with ease.
- A flexible data model to seamlessly configure and accommodate specific workflow requirements, avoiding costly customization.
- Customizable forms to manage participant data, samples, results, and clinical studies.
- Safeguard the Protected Health Information (PHI) of participants by assigning role-based data access to authorized personnel only.
- Maintain a read-only audit trail to track all laboratory activities along with a date and time stamp.
- Generate custom reports for quick and easy reporting of results to institutional review boards, NHS HSS, and the Clinical Trial Database.