Author: Compliancequest

Health, safety, environment, and quality, commonly referred to with the acronym HSEQ, refers to specializing in the health, safety, environment, and quality management of any organization. Health, safety, environment, and... Read More

Transform to a fully connected business with a next-generation AI-Powered Quality and Safety management platform, built on Salesforce. Our connected suite of solutions helps businesses of all sizes increase quality, safety... Read More

21 CFR Part 11 compliance is the FDA guideline that defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to that... Read More

Manage your entire document lifecycle with CQ document management solution to gain complete visibility and rely on a single source of truth across all organizational locations. Regulatory compliance is stringent.... Read More

ISO 9001 compliance ensures an organization is adhering to the latest requirements of ISO standards. ISO 9001 implementation drives operational excellence. Compliance to ISO 9001 needs automation and digital... Read More

Design control is a part of comprehensive quality standard set by FDA to assure medical device manufacturing risk free for users and patients. Design control starts with the development and... Read More

Job safety analysis (JSA) is a procedure that helps integrate accepted safety and health practices into a particular task or job operation. In JSA, the ultimate goal is to identify... Read More

FDA design control is defined as an interrelated set of quality practices and processes for medical devices design and manufacturing. FDA design controls make a systematic assessment of the design... Read More

Health and Safety Incident software to help centralize all your incident data, near misses, safety observations, fulfill CAPA and OSHA regulations. Furthermore, mitigate risks and prevent accidents by detecting a hazardous trend... Read More

The FDA Adverse Event Reporting System (FAERS) is a publicly available database containing information on adverse events and medication error reports submitted to FDA. The FAERS database, which follows FDA... Read More