Organizational Performance Management Table Essay

After you have completed your individual look into on your chosen type of health care organization, collaborate with your learnedness Team to complete this table. Then, summons to this table as you collaborate to write your paper. Include this table as an appendix to your paper.Fill in the necessary information in to each(prenominal) one cell, but be as succinct as possible.1. admit names of or links to specific organizations. Summarize key products or services provided by each type of organization and identify the primary customers they serve. governing One brass 2Organization one-thirdhttp//www.fda.gov/U.S. Food and Drug Administration2. Outline the overall content of the major linguistic rules, accreditation requirements, and other standards that affect each organization. Provide the title, section, parts, or subparts or the numbering system and so on of the specific regulations or accreditation requirements.For mannikin Use of electronic signatures in electronic medical records is equivalent to handwritten signatures on paper FDA regulation Title 21 CFR Part 11, Subpart C, 11.200 Electronic Signature http//www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=11Organization OneOrganization TwoOrganization ThreeFood and Drug Administration Safety and Innovation Act (FDASIA) Because of their importance, an agencys rulemaking plans are of great interest to a wide range to stakeholders. Therefore, the Federal Government publishes a semi-annual agendum of upcoming regulations in the Federal Register, usually in the Spring and Fall. As part of FDAs hydrofoil Initiative and FDA Transparency Results Accountability Credibility Knowledge Sharing (TRACK), we are excessively providing periodic updates on FDAs Unified Agenda rulemakings. On the Unified Agenda-TRACK Web page, we will maintain an updated agenda of FDAs Unified Agenda rulemakings.3. Highlight the effect of each organizations regulations, accreditation requirements, and other standards on the lay on the line- and quality-management functions and activities.Organization OneOrganization TwoOrganization ThreeThe scope of FDAs regulatory authority is precise broad. FDAs responsibilities are closely related to those of several other government agencies. Often frustrating and confuse for consumers is determining the appropriate regulatory agency to contact. The following is a list of traditionally-recognized product categories that fall at a lower place FDAs regulatory jurisdiction however, this is not an exhaustive list.In general, FDA regulatesFoods, includingdietary supplementsbottled waterfood additives sister formulasother food products (although the U.S. Department of Agriculture plays a lead role in regulating aspects of nearly meat, poultry, and egg products) Drugs,includingprescription drugs (both brand-name and generic)non-prescription (over-the-counter) drugsBiologics, includingvaccinesblood and blood productscellular and gene therapy productst issue and tissue productsallergenicsMedical Devices, including saucer-eyed items like tongue depressors and bedpanscomplex technologies such as heart pacemakersdental devicessurgical implants and prostheticsElectronic Products that deed over off radiation, includingmicrowave ovensx-ray equipmentlaser productsultrasonic therapy equipmentmercury vapor lampssunlampsCosmetics, includingcolor additives found in makeup and other personal care products skin moisturizers and cleansersnail polish and perfumeVeterinary Products, including blood feedspet foodsveterinary drugs and devicesTobacco Products, includingcigarettescigarette tobaccoroll-your-own tobaccosmokeless tobacco4. Specify components of performance-management systemspolicies and procedures, self-audits, benchmarking, unhealthiness management, corrective or preventive action, education and training, talk, and other mechanismsto be used by each organization.Organization OneOrganization TwoOrganization ThreeRisk communication st aff Our Risk conference Staffs objective is to assess and enhance FDAs approaches to effectively communicate the pretends and benefits of using FDA-regulated products. This includes providing lead in identifying, developing, conducting and promoting cross-cutting research, promoting understandable communication, and finding ways to improve the consistency and effectiveness of our communication approaches. This program also directs the activities of FDAs Risk Communication Advisory Committee, which was established to advise on strategies and programs to communicate the risks and benefits of FDA-regulated products so as to facilitate optimal use to review and evaluate FDAs and others research relevant to such communication and to facilitate interactively sharing risk and benefit information with the public to help people make communicate independent judgments about use of FDA-regulated products.Our major functions includeCoordinating development of agency policies on risk communic ation practices.Coordinating agency strategic planning activities concerning risk communications.Coordinating agency research agenda for risk communication methods.Facilitating development and sharing of risk communication best practices and standard operating procedures.Conducting risk communications research on methodological and cross-cutting issues.Leading management and coordination of the FDA Risk Communication Advisory Committee.Staffing and co-leading FDAs Communications Council5. Provide links to any relevant sources that will be useful as your Learning Team completes the paper.Organization OneOrganization TwoOrganization ThreeFda.gov