Production and Manufacturing Planning – Part 3
4-part FDA webinar series
This webinar series will identify the strategic steps for life science ventures to consider through during new research and development to ensure that their processes effectively align with US Food and Drug Administration’s approved standards. This FDA webinar series will be led by Jeff Skiba, Professional Medical Device and Business Consultant.
Description: This webinar will address process evaluation, production tooling and methods, contact points, how to set up raw material specifications, quality assurance and quality control. Participants can also expect to learn about measurement equipment, raw material control, use of limits as alerts, clinical outcome assessments and certificates of confidentiality. Reimbursement via CMS, and the Medicare and Healthcare Common Procedure Coding system will also be discussed.
Registration link: http://tinyurl.com/zdr92nb