Module 04 Written Assignment – Controlled Substance Record Keeping. Maria E. Acreman Rasmussen College Author’s Note This research is being submitted on July 29, 2012, for Instructor Stanley Sangar PT125/PTN2220 Section 01 Pharmacy Software/Automation/Insurance Billing. Controlled Substance Record Keeping The regulations for recordkeeping of controlled substances are the responsibility of the registered practitioner. The registered practitioner is not required to keep records of controlled substances that have been prescribed in the lawful course of their professional practice unless said controlled substances are prescribed for detoxification program or a maintenance program. The registered practitioner is required to keep records of any controlled substances that were administered in the course of detoxification treatment or maintenance program of an individual (Section VI – Record Keeping, n.d.).
Clinical Considerations FDA recognizes that clinical evaluation may be involved in the validation of the design of a modified device. Manufacturers are reminded that all clinical investigations must conform to the applicable regulations, including 21 CFR Parts 812, 50 and 56. Therefore, collection of clinical data to support a Special 510(k) may require submission of an investigational device exemptions (IDE) application to FDA. The fact that a significant risk device investigation was conducted to support any of the activities listed above, however, does not necessarily preclude the submission of a Special 510(k). 7 Manufacturers who intend to conduct clinical investigations of a modified device as part of design validation are encouraged to contact the appropriate ODE review division before preparing a Special 510(k).
HSC 037 Promote and implement health and safety in health and Social care Health and safety basically means assessing your workplace and reducing the risks. As an employee I have to abide by the health and safety at work act 1974. This means I need to attend any mandatory training I have been put on, go to supervisions, adhere to policies and procedures, use correct equipment, do not misuse faulty equipment, report any risks that I have seen and co-operate with my employer. This is all to ensure the safety of myself and others. My employer must follow the Management of Health and Safety at Work Regulations 1992, their responsibilities are to provide the mandatory training and supervisions, ensure policies and procedures are put in place, plan, organise, control, monitor and review health and safety arrangements, make sure the equipment is available and to maintain risk assessments and to deal with chemicals and other substances safely.
Per TJC standard, it states that, “The procedure site is marked by a licensed independent practitioner who is ultimately accountable for the procedure” (The Joint Commission, 2014). Again, the Chief Nursing Officer is responsible for ensuring all elements are included within the policy. First, all statements regarding the patient marking the site must be omitted. The policy must be revised to state that the LIP marks the site with the patient involved. It also needs to state that the mark is used with a skin marker that is specifically designed for skin marking and not use permanent marker (The Joint Commission, 2014).
IOM Social Care QCF Learning Centre Candidate Performance Evidence Record |Qualification/ unit 208 | |Candidate name: Enrolment No: | Use this form to record details of activities (tick as appropriate) Observed by your assessor Date observed: Seen by a witness Date observed: Self reflective account Date: NB your assessor may want to ask you some questions relating to this activity. There is a separate document for recording these. The person who witnessed/observed your activity must date and sign overleaf. |Unit |Learning |Assessment |Evidence | | |outcome(s) |Criteria | | | | | | | | | | |All employed staff have responsibilities toward health and safety in the work place. | |208 |1 | |The legislation that covers these responsibilities are | | | | |1.manual handling operations regulations 1992 | | | | |2.control of substances hazardous to heath 2002
The Scope of Practice of the Medical Assistant in Illinois The Medical Practice Act of the Illinois Department of Financial and Professional Regulation permits physicians to delegate certain clinical procedures and administrative functions to medical assistants. Every profession involves Such duties would include, giving injections (including immunizations), performing venipuncture, patient education, administering skin tests (including tuberculosis tests), calling in prescription refills as specifically authorized by the overseeing physician, entering physician-approved information verbatim into electronic medical records, and administering medications. Procedures which constitute the practice of medicine, or which state law specifically and unambiguously permits only certain licensed allied health care professionals to perform, however, may not be delegated to unlicensed personnel such as medical assistants. Medical assistants MUST always stay within their scope of practice. They must practice ONLY methods and procedures that are commonly accepted in their profession in which they were properly trained and supervised.
Check the appropriate box to indicate whether you have worker’s compensation insurance as required by state law. If applicable, attach proof. If not applicable, check N/A and provide an explanation. 22. “Printed name of provider”—print the last, first, and middle name of the provider as the sole proprietor, partner, corporate officer, or government official when applying to the Department of Health Care Services for enrollment or continued enrollment as a provider in the Medi-Cal program.
Hall v. Hilbun Betty Ford Rasmussen College Author Note This paper is being submitted on May 14, 2014, for Ann Nevers M230 Medical Law and Ethics Course. Hall v. Hilbun As a healthcare professional it is our duty to provide your patient with the best possible care. Standard of care means that the professional must exercise the type of care that a reasonable person would use in a similar circumstance (Fremgen, 2012, p.39). In the case Hall v. Hilbun, you are able to see the 4 Ds of negligence and how it can impact a patient and how it can be prevented. Dr. Glyn Hilbun, a general surgeon, examined patient Terry Hall who was complaining of abdominal pain.
IMPORTANCE OF IRB: UNIT 5 ASSIGNMENT Unit 5 Bobbie Roof 06/16/2013 HN410 – Human Services Delivery Angel Doring 1. What is an IRB? An IRB is a committee that performs ethical review of proposed research. The IRB or institutional Review Board is a federally mandated committee of administrators, medical doctors and community representatives to review and approve all research objectives, methodology, and protocols with special emphasis on plans for recruiting participants and gaining their consent (Royse, Thyer, & Padgett, 2010). The IRB exercises its responsibility to protect the rights and welfare of human participants in various categories of research in any way
Regulatory Agency Paper HCS/430 March 2, 2015 Christie Artuso Regulatory Agency Paper Regulatory agency within the healthcare industry, whether it be a government or any other type of agency all, have the same functions that are to protect and serve the people of the nation. This report will tell about the government regulatory agency known as the Federal Drug Administration or FDA for short. In detail will be what the agency is about, the structure of the agency, it will tell how this organization affects health care, show examples of how duties are carried out by the agency, it will discuss regulatory authority within the agency when it comes to health care and you, and lastly it will talk about the agency's process when it