Organizational Performance Management Table Essay Example for Free

administrational deed Management Table EssayAfter you have completed your individual research on your elect type of health care system of rules, collaborate with your Learning Team to complete this table. Then, refer to this table as you collaborate to write your paper. Include this table as an appendix to your paper.Fill in the necessary randomness in each cell, but be as succinct as possible.1. Provide 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. Organization OneOrganization bothOrganization triplethttp//www.fda.gov/U.S. Food and medicine Administration2. Outline the overall content of the major regulations, accreditation requirements, and other exemplifications 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 example Use of elec tronic 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 berths rulemaking plans are of peachy interest to a wide range to stakeholders. Therefore, the Federal Government publishes a semi-annual agenda of upcoming regulations in the Federal Register, usually in the Spring and Fall. As part of FDAs transparentness Initiative and FDA Transparency Results Accountability Credibility Knowledge Sharing (TRACK), we are also providing periodic updates on FDAs incorporated order of business 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 organizatio ns regulations, accreditation requirements, and other standards on the risk- and quality-management functions and activities.Organization OneOrganization TwoOrganization ThreeThe scope of FDAs restrictive authority is very broad. FDAs responsibilities are well related to those of several other government agencies. Often frustrating and confusing for consumers is determining the appropriate regulatory means to contact. The following is a list of traditionally-recognized product categories that fall under FDAs regulatory jurisdiction however, this is not an exhaustive list.In general, FDA regulatesFoods, includingdietary supplementsbottled waterfood additivesinfant formulasother food products (although the U.S. part of Agriculture plays a lead role in regulating aspects of some meat, poultry, and egg products) Drugs,includingprescription drugs (both brand-name and generic)non-prescription (over-the-counter) drugsBiologics, includingvaccines root and blood productscellular and gen e therapy productstissue and tissue productsallergenicsMedical Devices, includingsimple items like tongue depressors and bedpans multiform technologies such as heart pacemakersdental devicessurgical implants and prostheticsElectronic Products that give off radiation, includingmicrowave ovensroentgenogram equipmentlaser productsultrasonic therapy equipmentmercury vapor lampssunlampsCosmetics, includingcolor additives found in makeup and other personalised care products skin moisturizers and cleansersnail polish and perfumeVeterinary Products, includinglivestock feedspet foodsveterinary drugs and devices baccy Products, includingcigarettescigarette tobaccoroll-your-own tobaccosmokeless tobacco4. Specify components of performance-management systemspolicies and procedures, self-audits, benchmarking, complaint management, corrective or limp action, education and training, communication, and other mechanismsto be used by each organization.Organization OneOrganization TwoOrganization Thr eeRisk communication staff Our Risk dialogue Staffs objective is to assess and kindle FDAs approaches to effectively communicate the risks and benefits of using FDA-regulated products. This includes providing leadership in identifying, developing, conducting and promoting cross-cutting research, promoting understandable communication, and finding ways to improve the body 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 pertinent to such communication and to facilitate interactively sharing risk and benefit information with the public to help community make informed independent judgments about use of FDA-regulated products.Our major functions includeCoordinating development of agency policie s on risk communication 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 utile as your Learning Team completes the paper.Organization OneOrganization TwoOrganization ThreeFda.gov