Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development
June 8, 2015 - Fremont CA USCompliance4all
support@compliance4All.com
Phone:8004479407
Overview: This webinar focuses on how to establish a systematic approach to pharmaceutical development that is defined by Quality-by-Design (QbD) principles. In addition, this webinar teaches the application of statistics for setting specifications, assessing measurement systems, developing a control plan as part of a risk management strategy, and ensuring process control/capability. All concepts are taught within the product quality system framework defined by requirements in regulatory guidance documents. Learn How to: Implement QbD principles from discovery through product discontinuation Apply statistics to set specifications and validate measurement systems Utilize risk management tools to identify and prioritize potential critical process parameters Establish your design space Develop a control plan as part of a risk management strategy Ensure your process is in (statistical) control and capable. These are the same concepts detailed and explained by the Director of CDER at the FDA in a recently published (May 2014) paper in The American Association of Pharmaceutical Scientists. Why should you Attend: As stated in Q8, the ICH guidance document on pharmaceutical development, drug product should meet its intended product performance as well as meet the needs of patients. Although the strategy for pharmaceutical development may vary from company-to-company and/or from product-to-product, a systematic approach defined by quality by design (QbD) principles is required. Further guidance and policies have been provided to explain how the QbD approach should be integrated into the pharmaceutical quality system including process design, qualification, continued process verification, risk management, and validation. Although guidance on implementation of these requirements is prevalent, many companies have not yet implemented QbD into their quality systems; regulatory agencies have made it clear this will change. In fact, the chemistry, manufacturing, and controls (CMC) reviewers in the Office of Pharmaceutical Science (OPS) recently released a manual on policies and procedures (MAPP) explaining how reviewers will begin to enforce the requirements from these guidance documents. In fact, the Director of the Center for Drug Evaluation and Research (CDER) at the FDA recently (May 2014) co-authored a paper in The American Association of Pharmaceutical Scientists detailing the concept and reiterating the importance of using a QbD approach to pharmaceutical development. This webinar will demonstrate how to integrate those QbD principles into a pharmaceutical quality system. Compliance4All Adam Fleaming Phone: +1-800-447-9407 Event Link: http://bit.ly/1Hqybah support@compliance4all.com www.compliance4all.com