Why Should You Attend:
For many years, it has been more or less conventional wisdom that E&L data is a late-stage development concern, but current trends suggest this is changing. In recent months, the FDA has required multiple drug sponsors to provide detailed E&L packages and/or address specific questions in relation to E&L as early as Phase I. Questions have not only involved clinical trial container/closures systems, they also have signaled concern about equipment used in manufacturing of materials and devices used for dosing (i.e. infusion sets).
Unanticipated regulatory scrutiny has caused several programs to be placed on clinical hold pending submission of E&L data, resulting in development delays and unplanned expense. This presentation will review regulatory trends, the nature of questions sponsors have been required to answer, and the types of programs encountering these issues. It will also provide guidance on how to design phase-appropriate E&L programs to address early phase expectations.
Areas Covered in the Webinar:
Background and Overview of Extractables and Leachables
Regulatory Requirements of Extractables and Leachables
Current Regulatory Trends - Early Phase Development
Who Will Benefit:
Dr. Wayland Rushing is a technical expert in chemistry, manufacturing and controls (CMC) program design, analytical development and regulatory submissions. Over his 15-year career, he has led CMC development programs for a wide array of biopharmaceuticals, including parenterals, inhalation drugs, and other pharmaceuticals with complex delivery systems.
Dr. Rushing is a subject matter expert in HPLC and GC method development and validation, extractables and leachables program design and regulatory submission requirements; has drafted multiple IND and NDA submissions; and assists ABC clients in responding to FDA deficiency letters. He currently serves on Parenteral Drug Association (PDA) advisory committees for Technology Transfer and Elastomeric Closures and Seals Presentation Summary and was co-author of PDA TR 65, Technology Transfer.
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
PAYMENT METHOD: 100% Secure Transaction