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Consultation: Proposed clarification of the regulatory requirements for medical device systems and procedure packsV1.1 October 2019Therapeutic Goods AdministrationCopyright Commonwealth of Australia
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The purpose of consultation proposed clarification is to ensure that all parties involved have a clear understanding of the issue and can make informed decisions.
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Consultation proposed clarification must include specific details about the issue or topic in question, along with any relevant evidence or data.
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