Cloudbyz

JUNE 10, 2023

21 CFR Part 11 is a crucial component of regulatory compliance in clinical trials and, more broadly, any industry subject to the regulations of the U.S. This blog post will serve as a comprehensive guide to understanding and implementing 21 CFR Part 11 compliance in your clinical trials. Food and Drug Administration (FDA).

Compliance 98

Compliance Clinical Trials Clinical Trials Trials 98

Cloudbyz

AUGUST 8, 2024

Streamlined Workflow: Facilitates a seamless workflow by providing direct access to patient records and clinical data. Integration with Laboratory Information Management Systems (LIMS) Integrating Cloudbyz EDC with LIMS allows for efficient management of laboratory data, including test results, sample tracking, and workflow management.

Clinical Trials 52

Clinical Trials Clinical Trials Trials Compliance 52

Cloudbyz

AUGUST 26, 2024

The clinical research industry is in the midst of a digital revolution, with Clinical Trial Management Software (CTMS) at the forefront of this transformation. The Early Days: Legacy CTMS Systems In the early days of clinical research, managing trials was a manual, paper-based process.

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Clinical Trials Clinical Trials Trials Laboratory Information Management System 52