Healthcare professionals. Expenses incurred for treatments or consultations with the following healthcare professionals are reimbursed according to the terms indicated in the Schedule of Insurance, based on the module selected by the participant. The healthcare professionals must be members in good standing of a professional association recognized by the competent authorities or, failing the existence of such association, of a professional association recognized by the Insurer. Insureds may not receive more than one treatment or one consultation per day from the same healthcare professional, regardless of the number of specialties the professional practises.
Healthcare professionals. If you are a healthcare professional, you agree not to disclose any patient or other information prohibited to be disclosed under The Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy and Security Rules or other similar laws, rules or regulations, or to dispense any medical advice at any time during the course of your service as an Expert. You shall promptly notify us by emailing Xxxxxxx@Xxxxxx.xxx if, in your reasonable opinion, a Client is seeking to speak to you for any purpose other than to conduct research (e.g., attempting to obtain medical services or market products or services to you). You agree that you shall at all times comply with federal and/or state anti-kickback laws and other federal and state laws restricting gifts to and relationships with prescribers. You further represent to Zintro that you are duly licensed in all jurisdictions in which you are currently practicing, and that you are not listed on the List of Excluded Individuals/Entities issued by the Office of the Inspector General of the U.S. Department of Health and Human Services, the System for Award Management (XXX) and/or the Debarment List of the U.S. Food and Drug Administration. You agree that you will promptly notify Zintro in the event that any of the representations in this paragraph cease to be true. You understand and acknowledge that certain of our Clients may need to comply with federal and/or state reporting requirements including, without limitation, the Physician Payments Sunshine Act, a federal requirement applicable to manufacturers of drugs, biologics, devices and medical supplies to report any payments made to physicians and teaching hospitals to the Department of Health and Human Services (HHS) on an annual basis. If you participate in a Project for a reporting Client, you agree to provide information for this purpose including, among other things, a unique identifier such as your National Provider Identifier (NPI). You agree that all information that you provide for this purpose will be accurate and complete and acknowledge that such information as well as other information about you and the payment you received may be published on a publicly available and searchable website.
Healthcare professionals. A healthcare professional who provides services must be authorized to do so under government legislation and must be a member in good standing of a professional order recognized by appropriate legislative authorities. Moreover, a single treatment or consultation per day, per insured, is eligible for benefits.
Healthcare professionals. The following expenses are reimbursed at 100%, unless otherwise indicated.
Healthcare professionals. You agree not to participate in any engagement or its part thereof, the content or agenda of which are likely to include details of ● Any clinical trial which you are currently involved or have been involved in the last six (6) months, the results of which have not been disclosed. ● Patient experience of any clinical trials which you have been involved with or other information about patients to whom you have given medical advice Professionals: If you are a professional in the field of law, medicine, accounting, tax or any other regulated profession, you are prohibited from offering professional advice unless you have taken all steps to insure that the rendering of such advice through Imbibe Consultancy is done in strict accordance with the laws, guidelines, practices or rules governing or applicable to your profession. Inducements: Clients of Imbibe Consultancy are not allowed to influence your decisions pertaining to purchase, refer, use, dispense, recommend, lease of any products, devices or services, prescriptions of drugs. You are required to terminate the engagement and notify Imbibe Consultancy immediately if the clients attempt or perceived to have attempted to market their products or services, or influence your decisions, or induce or offer incentives inappropriately.
Healthcare professionals. Table 5: Summary of interviewees’ answers on selected questions Property Experience (1) IT familiarity (2) Current assess- ment method (3) Current assess- ment time (4) Resilience profile (5) Current support (6) Identified needs for resilience pre- dictions (7) Desired features of a resilience predic- tion tool (8) Output of tool (9) Frequency of use (10) Access by patient (11) Identified chal- lenges (12) Information needed during use (13) Clinical psycholo- gists 1 year None Distress thermom- eter (scale 1-10). Evaluation based on clinical in- terview. At every meeting with the patient. Strong dependence on social support; Resilience always changes over time. Bad resilience: Perfec- tionism. Do not ac- cept themselves. Lack of energy, strength. Sadness. Avoid fam- ily/friends Good resilience: See illness as an experi- ence to learn from. It manifests from the beginning. Patient can ask to refer to a psychologist Help to under- stand how the pa- tient responds to stress and reacts to different treat- ments Strategic game in which the patient chooses how they would react to some- thing. Risk cate- gories Early At each stage Yes, as long as the pa- tient want Substitute re- lationship with patient. Time spent on using the tool for patients and doctors. Technical/ sci- entific infor- mation. Easy way to see the re- sults. Provide infor- mation on changes in be- haviour of the patient over time. Nurses 10-20 years Good Do not know. Random. No guide- lines. No diag- noses or measures. At yearly clini- cal visits. The latest at the first-year fol- low-up. At visits re- quested by patient. Bad resilience: - Demanding, suspi- cious, -Sense of being sacri- ficed, bitter, fearful - Poor capacity to co- operate - Other concurrent life stressors (e.g. xx- xxxxx, caregiving, other illnesses, small children) Direct pa- tients to can- cer organisa- tions or to mental health services on a primary level. By social nurse and re- ferral to psy- chosocial unit. More efficient time manage- ment and work organisation. Allo- cate resources at right times to the right patients. Need for person- alized ap- proaches. Easy to manage and easy to use. Provide rec- ommenda- tions about patients. Data could automati- Colour coding of risks. Risk cate- gories. Early Con- stant feed- back/ recom- menda- tions Yes. Some patients would benefit. Readiness level of nurses and physi- cians to ac- cept and man- age such a tool. Familiarizing the personnel with the tool. Cannot say. User guidan...
Healthcare professionals. It is worth mentioning that the majority of healthcare professionals who participated in the inter- views have many years of experience on the field. The gap in resilience assessment was clearly identified along with the need for a tool assessing and predicting resilience in their work. In several cases, healthcare professionals expressed similar/common experiences and views. The following needs, requirements and challenges have been identified based on the survey analysis: Identified interactions - Monitoring the time-course of resilience level of a patient. - Receiving notifications of potentially significant changes in resilience level over time. - Filling in subjective, clinical rating of patient resilience by the physician. Identified user needs - Decision support toward the need to refer patients for personalized psychosocial interventions based on resilience assessment and prediction, in order to optimize resource allocation. Spe- cifically, grouping of patients by risk level seems to be the preferred way to receive feedback from the tool. - Help to measure, evaluate and predict patient resilience level before the treatment, after the treatment, and during the regular visits. - Support healthcare professionals in communicating resilience and associated factors to the pa- tient (and family). - Allow patient follow-up, e.g. assess effect of suggested intervention.
Healthcare professionals. Professionals from the DCH must also give informed consent for the experimentation to take place. They are expected to be on duty with a busy schedule during the experiment, so most of them should only walk across the waiting room while the robot operates and never interact with it. Nevertheless, some may wish to participate fully in the study, so this case is also planned for. The needs of professionals differ from the rest of the participants: they are easier to reach and are considered less vulnerable. Thus, instead of systematic one-to-one recruitment interviews, group information sessions will be organized during staff meetings to discuss the experimentation, during which investigators will answer workers’ questions about the robot and the protocol. Nevertheless, professionals will be given the opportunity to schedule one-to-one appointment with the PEG to discuss the experiment afterwards. Full participation of DCH professionals - Workers interested in participating will be given a full information note, providing all the necessary details about SPRING and the experimentation itself, including their rights as participants and regarding the collection, storage, transfer, process, and dissemination of the personal data collected during the experimentation, as well as the exploitation of the results of the study by the consortium’s members. Should they consent to interact with the robot and be interviewed by the researchers, they will sign a corresponding consent form, covering the entire duration of the study, as they will most likely be present on more than one day where the robot is deployed. Using the team schedule and the consent forms, the investigators will keep a record of who came in contact with the robot and when, so that relevant data can be erased afterwards if participants withdraw their consent. No participation of DCH’s professional, but no objection to the robot’s presence – For those who do not intend to interact with the robot, but consent to be in the waiting room while the robot operates, the investigator will issue notes of information stating their rights regarding the collection, storage, transfer, process, and dissemination of the personal data collected during the experimentation, as well as the exploitation of the results of the study by the consortium members. Should they consent to the robot’s presence, they will sign a corresponding consent form, covering the entire duration of the study, as they will most likely be present...
Healthcare professionals. Except as would not, individually or in the aggregate, have a Material Adverse Effect, each healthcare professional employed by the Company or its Subsidiaries or retained by the Company or its Subsidiaries on a consulting basis that has provided any clinical services to or on behalf of the Company or its Subsidiaries was at the time of providing the clinical services duly licensed or authorized, as applicable, to practice his or her profession in the state where such clinical services were rendered, as applicable, and each such healthcare professional that currently provides clinical services is duly licensed or authorized, as applicable, to practice his or her profession in the state in which such healthcare professional is performing clinical services. No event has occurred and, to the Company’s knowledge, no fact, circumstance or condition exists that has or reasonably may be expected to result in the denial, loss, suspension, revocation, rescission, probation or any other disciplinary action of or to any such professional license or authorization that would, individually or in the aggregate, reasonably be expected to have a Material Adverse Effect. Except as would not, individually or in the aggregate, reasonably be expected to have a Material Adverse Effect, no such healthcare professional: (i) has been sanctioned or disciplined by any licensing board or any other governmental agency or body, professional society, hospital, or commercial third-party payor, (ii) has had a final judgment or settlement without judgment entered against him or her in connection with a malpractice claim, (iii) has been found liable or responsible for any civil offense reasonably related to qualifications or competence relating to his or her professional practice, and/or (iv) has been terminated for cause related to a health care matter.
Healthcare professionals. (a) For the three (3) years immediately preceding the Closing Date or, if shorter, since such Person was hired by or began providing services on behalf of a Group Company, through and including the Closing Date, each physician, physician assistant, registered nurse or similar person employed by or providing services on behalf of the Group Companies (each, a “Healthcare Professional”), during the term of their employment or engagement by the Group Companies, has been duly licensed or certified and credentialed, as applicable, pursuant to applicable Legal Requirements and has held such medical staff privileges as required by any hospital or other healthcare entity (in each case for any periods in which services were provided by such Healthcare Professionals on behalf of the Group Companies) and such licenses, certifications or medical staff privileges have not been suspended, revoked or restricted in any material manner.
