The CSA program (Compliance, Safety, Accountability) is a key part of road safety in the United States. It tracks the performance of commercial drivers and trucking companies. If your score goes too high, it can lead to warnings, inspections, or even
Cleaning validation is a key part of pharmaceutical and medical device manufacturing. It proves that the equipment is clean enough before it is used again. One important step in cleaning validation is sampling, checking equipment for leftover product
Chlorine is a common chemical used in many industries, especially in water treatment, cleaning, food processing, and chemical manufacturing. While it is useful, chlorine can be dangerous if not handled properly. It can cause burns, breathing problems
When someone’s heart stops, every second matters. Cardiopulmonary resuscitation (CPR) can keep a person alive until medical help arrives. You don’t need to be a doctor or nurse to do CPR, even everyday people can make a difference.This guide explains
Blocking and cribbing are two basic but critical tasks in many industries, especially construction, emergency rescue, rigging, and heavy equipment work. The purpose is simple: support heavy objects safely while work is being done. But choosing the ri
Preparing for an FDA BIMO Inspection When the FDA notifies you of a Bioresearch Monitoring (BIMO) inspection, it can feel overwhelming at first. These inspections are designed to review the quality and
Food safety inspections play a key role in protecting public health. When violations are spotted and fixed, foodborne illness risks go down for everyone. This guide helps health inspectors spot and fix four major issues: employee hygiene, equipment s
Preparing for an FDA inspection is a serious part of running a pharmaceutical manufacturing facility. These inspections are done to check if your plant meets legal requirements and follows Good Manufacturing Practices (GMP). A successful inspection b
Clinical trials play a vital role in testing new drugs, devices, and treatments. These studies help determine if medical innovations are safe and effective. But behind every trial is a network of federal agencies responsible for protecting the public
Training microbiology lab staff on current Good Manufacturing Practices (cGMP) is one of the most important tasks a supervisor can take on. Clean lab practices, proper documentation, and correct testing techniques are all part of protecting product q
