Online Signature – How to Comply with the FDA 21CFR Part 11
What is the FDA 21CFR Part 11 The United States Food and Drug Administration (FDA) has a legal responsibility to ensure that medical devices are safe and effective. Therefore, in FDA-regulated industries, quality and accountability standards are much higher. One of the ways the FDA ensures quality in the industry is by requiring that records be kept of important aspects of the design, development or … Continue reading Online Signature – How to Comply with the FDA 21CFR Part 11