Discover the Future of Document Control & Training – Introducing PERFEQTA DMS

Discover the Future of Document Control & Training – Introducing PERFEQTA DMS

Introduction  PERFEQTA is a leading provider of innovative software solutions that help businesses of all sizes streamline their operations and achieve their goals. With a focus on customer satisfaction and continuous innovation, PERFEQTA is committed to delivering high-quality products and services that meet the evolving needs of its customers.  In today’s digital world, businesses are…

Things To Do In Nashville While Attending AABB Conference

Nashville, known worldwide as Music City, offers AABB Annual Meeting attendees more than just a premier venue for the key transfusion medicine event. Behind the convention center and meeting halls exist a city brimming with historical, cultural, culinary, and musical attractions for visitors to experience. This guide serves as a reference for AABB conference participants…

ISO 13485 Audit: Ensuring Compliance and Quality

ISO 13485 Audit: Ensuring Compliance and Quality

The ISO 13485 audit, also known as the certification audit, is a crucial step towards ensuring that medical devices meet regulatory requirements and international standards. Understanding ISO 13485 audit and its significance is essential for all stakeholders in the industry. In this blog, we will provide you with a comprehensive guide to ISO 13485 audit,…

Laboratory Quality Management System

Laboratory Quality Management System

The laboratory quality management system is an essential component of the modern laboratory. This system is designed to ensure that laboratories produce accurate and reliable results consistently. The system provides a framework for managing all aspects of laboratory operations, from personnel management to equipment maintenance. In this blog, we will dive into the key components…

Laboratory Document Control: A Comprehensive Guide

Laboratory Document Control: A Comprehensive Guide

When it comes to laboratory operations, document control is crucial in ensuring the accuracy and reliability of data. In this comprehensive guide, we will take you through everything you need to know about laboratory document control. From understanding its significance in a laboratory setting to deciphering the difference between documents and records, we’ve got you…

Quality Management in the Automotive Industry

Stringent quality control is crucial in automotive manufacturing. Defective vehicles can lead to expensive recalls, injuries, and irreparable brand damage. Automakers implement robust quality management systems (QMS) and “built-in quality” processes to achieve high reliability and consistent performance. Key elements of quality management in auto manufacturing include: Rigorous Parts Quality Suppliers are certified to standards…

Quality Management in the Medical Device Industry

Maintaining rigorous quality management systems and compliance is critical in the highly regulated medical device industry. Device makers must meet regulatory requirements while ensuring product safety and efficacy. Medical device quality management involves continuous process improvement, risk analysis, strong supplier controls, and extensive documentation. Here are 5 key elements of quality management for medical device…

The Cost of Quality: How to Measure and Reduce it

The cost of quality (COQ) quantifies the expenditures and losses associated with maintaining quality. Tracking COQ enables organizations to gauge quality program effectiveness and identify areas for improvement. Here are steps to measure and reduce your quality costs: 1. Define COQ Categories Typical categories include prevention costs (training, process improvement), appraisal costs (testing, audits), internal…

Transitioning from Manual to Automated QMS Processes

Many quality teams still rely on manual, paper-based systems that are inefficient in today’s fast-paced environment. Automating quality management processes brings immense benefits but also requires careful change management for adoption. Here are the best practices for transitioning from manual to automated QMS processes: Create a Detailed Implementation Roadmap Define each stage from initial training…