INTRODUCTION Good Laboratory Practices is defined in the “OCED ’’ principles as “ a quality system concerned with the organizational process and the conditions under which non clinical health and environmental safety studies are planned , performed , monitored , recorded , archived and reported ’’ . Good Laboratory Practices stresses on the importance of whatever the industry targets ie resources , characterization , rules , results , quality assurance .Good Laboratory Practices stresses on various places , studies etc . It applies on non clinical studies , medicines and health care products and many more . GLP stresses on the results which will demonstrate all the necessary things to be done to obtain appropriate report in respective …show more content…
The records generated during the procedure is the raw data , so one should not make the records on scraps of paper . The data collected should be recorded directly on the final form , the data can be a direct print out or in the electronic form.
3. While carrying out the procedure the data must be recorded as soon as the operation is done . It is not be acceptable to make the record after the procedure has been carried out . This will not be considered as accurate record .
4. Accurate timing should be noted down , otherwise it will lose the validity of the study .
5. Data should be proper that can be read and can be understandable otherwise it would raise many doubts .
6. One problem that gives rise to GLP was that data were been recorded in pencil and the subsequent changes were made without being evident .So under GLP , one should use waterproof ballpoint pens and also to check the robustness of machine printouts as it sometimes disappears quickly . At times if these happens then a photocopy with signed and dated is acceptable for storage .
7. The basic tenets of GLP is the need for a record to be signed by a person who did the job on a study .
8. Also, the dated records with signature indicates the procedure was recorded at correct time in the study
Make sure that all communication is legible. During time sensitive situations such as codes, one person needs to be designated as the time or record keeper. Also, code sheets keep everything in a chronological order. During these situations, using the same watch is imperative. Noting exactly the name of the physician that is paged and when the page is returned is important to document.
Low-Risk level encompasses simple admixtures involving closed-system transfer, measuring, and mixing of three or fewer sterile products. Some of the things low-risk compounding include are, CSPs are compounded using aseptic technique within an ISO Class 5 PEC that is located within an ISO Class 7 buffer area with an ISO Class 8 ante area. Each container, including the final container, cannot be entered more than twice to prepare the CSP. There is a limitation to aseptic manipulations of disinfected containers using sterile needles and syringes. Medium-Risk level encompasses preparations requiring more complex compounding processes.
(Hogue & Prudhomme, 2012) Another point is documentation on a patient. There is a saying in the medical field if you didn’t document it didn’t happen, make sure as a case manager, everything you do is fully documented in the patient record. Develop habits that are good, you always want to document on a client when everything is fresh. It proves to the case manager’s credibility.
Task 3 1. Why it important to work accurately and what is are the consequences of submitting inaccurate results? It is important to submit accurate results as the results that are submitted could potentially be used in a legal scrutiny case in court to help prosecute the offending company. The reason why the quality of the results must be so accurate is because if case goes to court the accused company will want to challenge the work you have carried out or your method or your results, they will employ a solicitor to help them win the case.
The publisher’s intended audience are people who advocate for the rights of animals and are searching for different methods of testing products. The purpose is to inform the people that animal testing is “old school” compared to the new innovative ideas. They want the people to be aware that these experimentations are not successful with the animals nor when they are tested on humans.
Activity to be Audited 5.4.3 Request Form Information: a) Does the request form contain: I. Forename and surname II. Gender III. Date of birth IV. Address V. Hospital number b) Name or other unique identifier of clinician or other person legally authorized to request examinations & Destination of report: c) Type of primary sample and the anatomic site of origin, where appropriate; d) Examinations requested; e) Clinical information relevant to the patient, which should include gender and date of birth, as a minimum, for interpretation purposes; f) Date and time of primary sample collection; g) Date and time of receipt of sample by the laboratory.
The time was recorded to the nearest hundredth of a second. A week later, the same procedure was followed with each athlete receiving a different treatment from the week
6.Current Status of EHR ,Issues and its Future Implementations for its Expansion EHR is an integral segment of the transition to computerized documentation. The digital wave should be embraced to upgrade the healthcare disparities of Americans. To address the future of health care in the 21st century, the employment of electronic health records is crucial and will lead to preferred element outcomes for the patients. As technology continues to improve into the health care realm, the EHR will explode and advance capability of customer services .The transition must yield successful outcomes that may easily accomplished by invoking better medication choice for the providers using EHRs.
To conduct the lab, information regarding
In the previous decades, a smoked paper was used as the recording sheet. Today, as we advance, we sometimes use sheets of graphing paper or plain paper. On some instances a manual procedure is done but since we already advanced in technologies, we now use software for
Purpose: To inform the audience about animal testing I. Introduction A. Attention getting device: Approximately 26 million animals are used every year in US laboratories for cosmetic and biomedical research. B. Thesis: I would like to inform you about how animal testing is conducted. C. Credibility: I have read and studied the articles about animal testing. D. Preview: I am going to share with you purposes of animal testing, how animals are used in laboratory tests, and the effectiveness of animal testing.
Task 1 Outcome 1: 1.1) a. The problem of using the manual system is high cost. And the manual system is not convenient at all for both staff and customers. Staff must record the data of all the things manually on the log book. The number of customers is increasing, so staff must to do more works or the library need to hire more staff.
It is important to examine these issues before experimental practices become casually introduced. Issues including
The practice of animal testing is a very debatable topic. “Each year, more than 100 million animals, including mice, rats, frogs, dogs, cats, rabbits, hamsters, guinea pigs, monkeys, fish, and birds are killed in U.S. laboratories” (Experiments). “The term “animal testing” refers to procedures performed on living animals for purposes of research into basic biology and diseases assessing the effectiveness of new medicinal products, and testing the human health and/or environmental safety of consumer and industry products such as cosmetics, household cleaners, food additives, pharmaceuticals and industrial/agro-chemicals” (About). There is numerous pros and cons for using animals in experiments for humans for our everyday needs. There is different pros for animal testing including helping researchers to find drugs and treatments, help ensure safety of drugs, there are no other testing alternatives, and it provides an opportunity to examine a complete life cycle.
ANIMAL TESTING IN LABORATORY SHOULD BE BANNED MIAO Jingwen (Betty) St. No.: 15250210 GCPS 1005, Section 00014 15/03/2017 Instructor: Dr. Michelle Huang Specific Purpose: To persuade the audience that animal testing in laboratory should be banned. Introduction (attention getter)