Join us for this popular webinar as we delve into the various methods used to establish the minimum sterilization dose for medical devices and other sterile products. This webinar will provide a thorough understanding of the selection process for a dose establishment method, the criteria for choosing representative products for testing, and the calculation of the verification dose.
The webinar begins with an exploration of the multiple methods available for establishing the minimum sterilization dose, including Method 1, VDmax, and Method 2. Each method has its unique applications and advantages, and understanding these differences is crucial for selecting the most appropriate approach for your specific needs. The presentation will offer detailed insights into each method, helping you determine which is best suited for your products and processes.
Next, we will discuss the importance of selecting a representative product for testing. This step is essential to ensure that the sterilization dose is effective across all products in a given category. The criteria for choosing a representative product will be explained, along with practical examples to illustrate the process.
The calculation of the verification dose is another critical component of the sterilization dose establishment process. The webinar will guide you through the steps involved in this calculation, providing clarity on how to achieve accurate and reliable results. This section will include a review of the mathematical principles and considerations necessary for determining the verification dose.
Additionally, the webinar will cover activities to ensure the continued effectiveness of the established sterilization dose. Maintaining sterility over time requires ongoing monitoring and validation, and this presentation will provide best practices for these activities. You will learn how to implement effective strategies for dose verification and maintenance, ensuring that your sterilization processes remain compliant and effective.
This comprehensive webinar is ideal for professionals involved in sterilization, quality assurance, regulatory compliance, and product development within the medical device and pharmaceutical industries. Gain valuable insights into the methods for establishing the minimum sterilization dose, understand the importance of selecting representative products, and learn best practices for maintaining dose effectiveness.