Master Consulting Agreement
$119.00
$119.00
per item
Master Consulting AgreementThe Master Consulting Agreement is a robust and mature agreement designed specifically to support medical device consultants. This product is a must for individuals or companies entering the medical device consulting field.
Master Consulting Agreement OverviewThe Master Consulting Agreement addresses a wide range of topics such as the following:
For more information regarding our Master Consulting Agreement please contact us at [email protected]
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The Medical Device Quality Agreement for US defines the individual responsibilities of the parties as to the regulatory and quality aspects of a medical device intended for distribution in the United States. The Quality Agreement is intended to be used to define the division of responsibilities between the parties and to demonstrate their compliance with applicable regulatory requirements of the United States Food and Drug Administration (FDA).
Medical Device Quality Agreement for Europe
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The Medical Device Quality Agreement for Europe includes required agreement content and defined responsibilities between a manufacturer and a distributor of medical devices per the legal requirements specified in Medical Device Regulation, MDR (EU) 2017/745 and ISO 13485:2016.
Master Consulting Agreement
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