At MCRA we closely follow legislative and regulatory development so we understand how they will impact your business. Regulators, Boards of Directors, employees and customers require and expect healthcare organizations of every size and type to have compliance policies and procedures that support the detection, prevention, and remediation of non-compliant business activities.
Well-drafted and fully implemented policies and procedures demonstrate an organization's commitment to ethical business practices. Creating and maintaining these programs is challenging for every manager. MCRA can assist in the creation and implementation of required policies and procedures to help you quickly identify compliance issues and develop a corrective plan of action. MCRA provides employee training and education that covers federal healthcare compliance requirements. We can also provide required training for your Sales Team and Board of Directors.
Conflicts of interest often arise in healthcare, particularly with complex financial relationships and during research related activities. MCRA can assist in evaluating whether there is an actual, potential or perceived conflict of interest.
If so, MCRA can provide a comprehensive management plan created to proactively address questions that may arise regarding an individual's objectivity, integrity or professional commitment as the result of a disclosed activity, relationship or financial interest. The incumbent, member of the broader EMEA Legal, Regulatory and Quality Team, will also support expansion in new markets and will be an active member of the African management team. Click the "Apply" link to let us know you are interested.
Not the right fit? Please consider joining our Talent Network to receive notifications about future jobs or sharing this opportunity with others in your network. Share this offer with your network. Legal Counsel, Africa Medical devices. Published on Share this offer. Review contractors assess compliance with the face-to-face encounter and written order prior to delivery requirements. Some items such as PMDs have statutorily imposed requirements. For items that do not have statutory requirements, a face-to-face encounter and written order is required only if the item is selected from the Master List and placed on the Required Face-to-Face and Written Order Prior to Delivery List.
Items selected for the list will be published in the Federal Register with a day Notice Period. CMS may suspend the face-to-face encounter and written order prior to delivery requirements generally, or for a particular item or items, at any time and without creating a new rule, except for those items included on the Master List due to statutory mandate.
CMS may suspend the face-to-face encounter and written order prior to delivery requirements generally, or for a particular item or items, at any time and without creating a new rule--except for items included on the Master List PDF. We will post this list here when the requirement is in effect again. HHS is committed to making its websites and documents accessible to the widest possible audience, including individuals with disabilities.
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