B. Scientific data COSHH records hold information in relation to risk assessments, safety data sheets and how you can work with various hazardous substances, it ensures that all companies follow health precautions to make staff members safe. They are non-confidential information as all staff members should be allowed to access them, yet their extremely important detailed records which must be kept safe, so they should be stored within an office or a locked filing cabinet. They will be used when required so having them on the PC will be practical, for example when changes occur on when an evaluation of the COSHH records happen. The reason for keeping these types of records is that they’re only updated when it’s important and it allows all staff members to become more knowledgeable about things relation to the COSHH register. www.hse.gov.uk/coshh/ Scientific data is usually a long-term archive storage which holds various scientific methods, whereas it can also be data collected from experiments within the laboratory. The scientific results found should be easily accessible and they should follow …show more content…
safe working procedures. It should be stored in an accessible area so that staff can use their information as it’s not confidential, it’s just important when evaluating an experimenting or when finding different scientific methods to use. These will usually be a paper copy so that they’re accessible to everyone. It will only be accessed on rare occasions when required and it should be kept because this long-term data needs to be used by staff members when needing to access important scientific information. https://en.wikipedia.org/wiki/Scientific_data_archiving Scientific apparatus records are important information records which are stored safely within a laboratory environment. These records control the perchance and maintenance of every equipment piece which is bought. This paper copy information should be stored within a safe filing cabinet or with the HR department, it will be changed when information relating to the science workplace has changed or when updates need to occur. This type of information should be kept as it enables staff to know about stock figures and what needs to be ordered if something goes wrong for example. https://quizlet.com/20980657/btec-applied-science-data-storage-flash-cards/ Quality assurance records holds information about equipment to ensure that everything is fit for purpose and ensures that manufactured products are safe to use and won’t cause problems when used within a laboratory, it ensures that quality procedures are followed. This information could be stored on the PC so that they can be easily updated, they can be stored within the laboratory office or within the HR department online records. These records will only be updated when changes occur, it’s important to keep this information safe as it ensures that quality assurance is paramount within the science environment and it informs all staff members with knowledge about quality assurance. https://en.wikipedia.org/wiki/Quality_assurance Laboratory test data is information which has been gathered after completing a scientific procedure, this information will need to be accessible for all staff members for when completing experiments in the future or when writing an evaluation for a particular experiment. It should be stored within an office or even a locked filing cabinet inside a laboratory, it will be accessed on a regular basis as people may decide to update the records when completing an experiment. This data should be kept as it ensures that all staff are informed about knowledge of various experiments and it allows them to put data on a specific record document. http://medical-dictionary.thefreedictionary.com/laboratory+test Sample throughput and management is there at any point in the process within a scientific laboratory, it ensures that everything is done effectively.
For example, if a blood sample was taken at the doctors, sent to the hospital and then the results were given to the doctor’s surgery; this involves sample throughput and management as everything is control and good working practises are promoted. This information will usually be accessible to all members of staff, yet it could be updated regularly when procedures change, so putting it on the PC would be practical. It could be stored within a laboratory office or even within a safe folder in a filing cabinet. It will be accessed rarely as it will only need when required, this information should be kept as staff should be allowed to follow regulatory procedures so that processes are safe and are completed
effectively. http://www.labmanager.com/laboratory-technology/2010/02/improving-sample-throughput#.VuAhrU1WLAU http://www.termpaperwarehouse.com/essay-on/M1-Explain-The-Different-Processes-Involved/354136
The data utilized for trial analysis are maintained anonymous, however the trial management data carry personal identifiers for conduct of study and to ensure patient safety. The patient source data is encrypted and password protected allowing access to authorized personnel and prevents transfer to electronic media device. The list of authorized personnel will be maintained in the Trial Master File. The audit trails captures all activities pertaining to conduct of clinical trials and tracks changes performed to data. The date and time stamp used impede chances of misuse. On completion of the trial, the data will be locked using DMS file locking facility to prevent tampering of
Workplaces must keep suitable and accurate records required by the regulations of RIDDOR; these records help to identify patterns in accidents and injuries and will help when risk assessments are carried out. Personal records of employees must also be kept, but must be kept confidential in order to comply with the Data Protection Act. In the event of work-related claims workplaces may also insure they keep all their records and information as insurance company will want to see these records.
Medical facilities have to follow certain guidelines. They have to insure patient’s privacy in all areas. The medical facility has to protect the patient medical records and all healthcare information for the patient. If paper files are still in use at the medical facility, it should be stored, where it can be locked at close of business. Also, medical files should not be kept where individuals, other than those that need to use them, have access to them. Electronic medical records are being pushed for all facilities, large or small. The thought is less chance of someone having access that should not. There are firewalls, password use, encryption and other means of protecting electronic health records.
Recognizing the advantage of computers that were now able to obtain electronic files, Congress called for a more standardized approach in regards to storing patient information. Under HIPAA, the idea was that creating a standard system would increase flexibility when communicating between hospitals, clinics, and insurance companies, providing more time to be spent on the quality of patient care that was being provided. In addition, the goal was that electronic record storage would allow instant tracking and analysis of data in order to cut down costs and easily access trends that could have major impacts on patient care.
...nce an incident that may not be seen as such by staff working in the same environment but, if the staffs have frequently witness that the same incident occur; they may stop reporting the incident. However, database application system can save charting time which could be utilized to provide care to residents. Administration function like medical records, risk assessments, daily reports and coding requires documentations from the service users` electronic medical record database to enhance the EHR, which link the EHR data with databases containing standardized assessment information from external healthcare systems. If the database is not similar as to what other healthcare systems use, it is impossible to share information from EHR database with other clinical application systems.
Every patient's medical records are different some contain more information due to their medical history. If a patient has alot of problems and have been treated then their file would have more information . Certain records also contain history of complaints and procedure, few records have photographs with a short summary of what is present. Medical records can be electronically stored , traditioanlly handwritten and even voice recorded. Medical records that are written on paper and kepted in folders are divivided into informative sections It contains medical terminology terms that any person in the medical field can read It should be written in either black or blue ink. Each provider should always document the evaluation and results of every visit during the visit. It is prohibited to pre-date or backdate an entry. If there is to be a mistake written in a wrong patients file it should be dated and signed by the person that is revising the file; this shows proof that it was corrected..
In the modern era, the use of computer technology is very important. Back in the day people only used handwriting on the pieces of paper to save all documents, either in general documents or medical records. Now this medical field is using a computer to kept all medical records or other personnel info. Patient's records may be maintained on databases, so that quick searches can be made. But, even if the computer is very important, the facility must remain always in control all the information they store in a computer. This is because to avoid individuals who do not have a right to the patient's information.
In any healthcare organization, data is collected in numerous ways for an ever-increasing number of reasons. Data may be collected by a monitoring device directly connected to the patient, or by providers as they make observations or record treatments. Quality improvement activities often call for data collection where observations of activities, timeliness, or satisfaction indicators are gathered. Data may be abstracted from primary sources and collected for unique reporting requirements, such as specialized registries or claims transactions. With the various types of data collected in many different methods for varied purposes, it is not surprising that data collection may have escaped management in the past.
Medical information should be stored in a private place, with that being said as soon as it get typed or either wrote it should get put away immediately. With this being said important typed data should be timed and date stamped and the person that typed the information should be identified in the medical record. “Back-up systems” should be used for this typed data just so it won’t be loss. Make sure you have it put up with security around.
Health information management involves the practice of maintaining and taking care of health records in hospitals, health insurance companies and other health institutions, by the use of electronic means (McWay 176). Storage of medical information is carried out by health information management and HIT professionals using information systems that suit the needs of these institutions. This paper answers four major questions concerning health information systems.
Maintenance of Records - ensures all Employment Equity records are maintained in a secure fashion to ensure strictest confidentiality.
Science is the observation of natural events and conditions in order to discover facts about them and to formulate laws and principles based on these facts. Academic Press Dictionary of Science & Technology --------------------------------------------------------------------- Science is an intellectual activity carried on by humans that is designed to discover information about the natural world in which humans live and to discover the ways in which this information can be organized into meaningful patterns. A primary aim of science is to collect facts (data).
A HIRA should be specific, suitable and appropriate to the nature of the activity identified and be accountable to a certain extend (Schoeman and van den Heever, 2014; NOSA, 2010). A HIRA can be kept for record purposes as this will assist in the alteration of certain work processes, procedure or even establishing new infrastructure (MHA, 1996). A HIRA can be a basis document used to prevent any faulty activity, build more moral in an establishment as employees enjoy working in a safe environment, and encourage safe practises by employees who can yield more production time that can be beneficial to the employee and employer (Harmse, 2007; Brandsæter, 2002 ).
include, but are not limited to; keeping detailed records of patient medical history and symptoms,