Safeguarding Patients: Test Method Validations

This DDL webinar discusses the critical importance of test method validations in the healthcare packaging industry. It highlights how these validations are often misunderstood and not executed correctly, leading to significant implications for patient safety.

Key points covered in this webinar include:

• The necessity of understanding the impacts and risks associated with test method validations.
• Key considerations such as equipment validation, sample preparation, and environmental factors that can influence the reliability of test data.
• The need for unbiased sample creation and maintaining a distraction-free testing environment to ensure accurate results.
• The importance of compliance with industry standards and the development of robust test method procedures.
• The need for internal protocols tailored to specific organizational requirements.
• The significance of continuous improvement, even after initial validations are performed to adapt to changes over time and enhance patient safety.

In conclusion, reliable data from test methods can only be obtained through proper validation processes, and having a continuous improvement mindset is paramount in maintaining patient safety in all testing procedures.

Please fill out the form to receive a copy of the webinar recording.