FDA inspections check that companies comply with the regulations and quality standards that apply to them, and even well-run firms can receive a Form 483 or warning letter. Because responses are due within 15 days, there is little time to work out what the agency expects.
This 90-minute FDA 483 and warning letter response training explains why a robust, timely response matters and the risks of an inadequate one. You'll learn the elements of a thorough response, how to structure it to meet FDA expectations, and how to use a response checklist.
The session also reviews recent regulatory observations and the responses to them, the submission process, when and how to send follow-up updates, and planning for post-response outcomes.
A weak or late response to a 483 or warning letter can lead to further regulatory action, so it pays to know what to include and how to present it before you need to.
This session is valuable for anyone involved in developing, manufacturing, selling or distributing FDA-regulated healthcare products, and is a good primer for quality, manufacturing and engineering staff who write observation responses.
This course will be valuable to anyone engaged in the development, manufacturing, sale, or distribution of FDA-regulated healthcare products. Additionally, this course will provide a good primer for those involved in writing observation responses. This includes personnel in:
A weak or late response to a 483 or warning letter can lead to further regulatory action, so it pays to know what to include and how to present it before you need to.
This session is valuable for anyone involved in developing, manufacturing, selling or distributing FDA-regulated healthcare products, and is a good primer for quality, manufacturing and engineering staff who write observation responses.
This course will be valuable to anyone engaged in the development, manufacturing, sale, or distribution of FDA-regulated healthcare products. Additionally, this course will provide a good primer for those involved in writing observation responses. This includes personnel in:
Kelly Thomas
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
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