Nanomaterials are materials consisting of particles, molecules, or ions with dimensions between 1 and 100 nanometers. They possess unique properties compared to their traditional counterparts because of their atomic-scale size.
GMP regulations are guidelines to ensure that pharmaceutical, biotech, and medical device products are safe, effective, and high-quality. These regulations are enforced by regulatory bodies such as the FDA and EMA.
A lockout/tagout procedure is a safety protocol used in various industries to ensure the safety of workers during the maintenance or repair of machinery or equipment.
Safety performance is the analysis of safety processes and procedures to determine how well those systems function. It involves checking the levels of risk, identifying potential hazards, evaluating safety policies and regulations, and carrying out accident investigations.
Original Article: https://safetyculture.com/topics/safety-leadership/ What is Safety Leadership? Safety leadership is a management approach that prioritizes employee safety in the workplace….
The costs associated with making sure that your product is of good quality are called quality costs. It includes preventing, detecting, and fixing any issues with the product.
MDSAP, or Medical Device Single Audit Program, is a joint initiative between Australia, Brazil, Canada, Japan, and the United States regulatory bodies.
Quantitative risk analysis uses numerical data to identify and measure the potential risks of a project or business decision.
Qualitative risk analysis evaluates the likelihood and impact of risks on a project or organization. It involves identifying potential risks, assessing their probability and effect, and categorizing them based on severity.
The ISO 9004:2018 standard is a set of guidelines for businesses looking to improve their overall performance. It focuses on eight key areas: customer satisfaction, leadership, engagement of people, process management, continual improvement, business results, and supplier relationships.