Training: Driving Quality and Compliance in the Healthcare Industry

QR Group offers a series of specialized training to enhance quality systems in medical device manufacturers, aiming at compliance with standards such as RDC 665/2022, ISO 13485, ISO 14971 and CAPA processes. Our goal is to train employees to monitor risks, measure performance, and ensure continuous improvement in regulatory and operational processes.

Why invest in quality-assured training

Training the team in good manufacturing practices (RDC 665/2022) prepares the company to meet ANVISA requirements, reduce waste, and avoid failures in production processes. The implementation of the quality management system based on ISO 13485 strengthens competitiveness, as it allows the company to act with excellence in Brazil and in international markets. Training in risk analysis (ISO 14971) and corrective and preventive actions (CAPA) enables the team to effectively identify, prevent and correct deviations.

Structure and expected results of training

Our program is complete: we start with mapping the current quality system, identify gaps and define practical action plans. The sessions include exercises, case studies and technical discussions, all to ensure that the knowledge is applied in the day-to-day life of the company and results in safer, more efficient and compliant processes.

This methodology has raised the quality bar for countless clients, reflected in certifications, smoother audits, and improved operational productivity. In addition, it strengthens the internal culture of continuous improvement and reduces regulatory vulnerabilities.

Contact the QR Group team and find out how our training in quality management systems can transform your company’s performance in the healthcare sector, increasing compliance, efficiency, and competitiveness.

Source: QR Group