Health Resources Sample Clauses

Health Resources. Inc. and Vendor acknowledge that certain confidential and proprietary information may be disclosed by one of them to the other in the course of this Agreement. For purposes of this Agreement, the term "Confidential Information" includes the following: (a) All information regarding the patient, Health Resources, Inc's. Customer, any patient medical data and/or status, or provider information; and (b) any other information identified as confidential in writing by the disclosing party prior to disclosure. Notwithstanding the confidentiality requirements of this Agreement, the foregoing shall not prevent Health Resources, Inc. from retaining information, including any and all information and data pertaining to any patient which comes to Health Resources, Inc. or to which Health Resources, Inc. is given access during this Agreement.
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Health Resources. Access to Blue Advantage online health resources.
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Health Resources. While they are few in number and some were unfamiliar to the FGDPs, there are a handful of health resources available to help farm workers in the southwest Georgia community deal with the diet-related health conditions facing them. Not surprisingly, there were some commonalities in the discussions about barriers to accessing healthy food and barriers to accessing these healthcare and health resources. The local migrant health clinic, for example, offers a holistic approach to health that encompasses clinical care and health education. KI-1 highlighted the clinic’s nutrition education course; however, members of only one of the three FGDs were familiar with this program. Meanwhile, KI-3 mentioned the role of the Red Cross, Mental Health Services, and other organizations in referring people to the food bank. He estimated that most farm workers who use the food bank are referred by Mental Health Services. During the FGDs, participants were familiar with the clinic’s basic services but (in general) did not express knowledge of extra programs or outside organizations. The FGDPs and the key informants alike acknowledged that, while there are a handful of health resources available to them, farm workers are often not informed about their existence and encounter many barriers when trying to access these resources in southwest Georgia. Several women said that their families frequently did not have enough money to buy everything they needed/wanted; childcare and medical attention were mentioned as priorities that must often be foregone. It is possible that there is a sort of “feedback” cycle wherein some women do not go to the clinic often due to financial constraints, and therefore, those same women do not have the opportunity to learn about the clinic’s full range of services. Discussion and conclusion Summary of study Study design and goals. The current study used a cross-sectional mixed methods design to understand the associations between food insecurity, diet diversity, and health outcomes, including anemia, elevated/high blood glucose, hypertension, and overweight/obesity, among migrant farm workers in southwest Georgia and the ways in which these farm workers perceive their own health and access to healthy food. A high prevalence of both food insecurity (66.1%) and low/medium dietary diversity (61.3%) was observed. Additionally, in the surveyed subset, 22.4% were hypertensive, 49.4% were anemic, 33.5% had high blood glucose and additional 41.1% had elevated ...
Sample 1

Related to Health Resources

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  • Clinical Data and Regulatory Compliance The preclinical tests and clinical trials, and other studies (collectively, “studies”) that are described in, or the results of which are referred to in, the Registration Statement or the Prospectus were and, if still pending, are being conducted in all material respects in accordance with the protocols, procedures and controls designed and approved for such studies and with standard medical and scientific research procedures; each description of the results of such studies is accurate and complete in all material respects and fairly presents the data derived from such studies, and the Company and its subsidiaries have no knowledge of any other studies the results of which are inconsistent with, or otherwise call into question, the results described or referred to in the Registration Statement or the Prospectus; the Company and its subsidiaries have made all such filings and obtained all such approvals as may be required by the Food and Drug Administration of the U.S. Department of Health and Human Services or any committee thereof or from any other U.S. or foreign government or drug or medical device regulatory agency, or health care facility Institutional Review Board (collectively, the “Regulatory Agencies”); neither the Company nor any of its subsidiaries has received any notice of, or correspondence from, any Regulatory Agency requiring the termination, suspension or modification of any clinical trials that are described or referred to in the Registration Statement or the Prospectus; and the Company and its subsidiaries have each operated and currently are in compliance in all material respects with all applicable rules, regulations and policies of the Regulatory Agencies.

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