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MCL Medical Center of Louisiana Point of Care Testing Urine Pregnancy Test --Patient Result and Quality Control Documentation Form both controls must be documented with each patient Year Date Medical
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How to Fill Out Printable Control Logs:

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Start by gathering all the necessary information that needs to be recorded in the control logs. This may include relevant dates, times, locations, and any specific details required for the control logs.
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Open the printable control log document on your computer or print out a hard copy if necessary.
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Begin with the first entry on the control log. Fill in the appropriate fields, such as the date, time, and location. If there are any specific instructions or fields to be filled out, follow them accordingly.
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Continue filling out each entry on the control log, ensuring accuracy and completeness in recording the required information. Pay attention to any specific formatting or instructions provided.
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Keep the completed control log in a safe and easily accessible location for future reference or auditing purposes.

Who Needs Printable Control Logs:

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Professionals or businesses involved in quality control or compliance measures may require printable control logs to monitor and track various processes, test results, or equipment maintenance.
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Manufacturers and production facilities can utilize printable control logs to document production runs, critical parameters, and quality checks to ensure consistent product quality.
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Healthcare providers such as hospitals, clinics, and laboratories may use printable control logs to record patient information, medication administration, test results, or other healthcare procedures for accurate record-keeping and regulatory compliance.
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Point the absorbent tip (with 5 small openings) directly into the urine stream. Take the sample for at least 7-10 seconds, to ensure that an adequate sample is collected by the testing device. (Another technique is to collect the urine into a clean container and dip half of the absorbent pad for at least 10 seconds.)
Storing a urine sample Do not keep it for longer than 24 hours. The bacteria in the urine sample can multiply if it is not kept in a fridge. If this happens, it could affect the test results.
C. If not tested immediately, urine may be stored at room temperature (59-86oF or 15-30o C) or 8 hours refrigerated at 36─46oF (2─8oC) for up to 3 days. Samples must be brought to room temperature before testing.
Point the absorbent tip (with 5 small openings) directly into the urine stream. Take the sample for at least 7-10 seconds, to ensure that an adequate sample is collected by the testing device. (Another technique is to collect the urine into a clean container and dip half of the absorbent pad for at least 10 seconds.)
First morning urine samples will normally contain the highest levels of hCG. C. If not tested immediately, urine may be stored at room temperature (59-86oF or 15-30o C) or 8 hours refrigerated at 36─46oF (2─8oC) for up to 3 days. Samples must be brought to room temperature before testing.
It appears shortly after the embryo attaches to the wall of the uterus. If you are pregnant, this hormone increases very rapidly. If you have a 28 day menstrual cycle, you can detect hCG in your urine 12-15 days after ovulation.

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Printable control logs are used to record and track the handling of controlled substances or materials within an organization, ensuring compliance with regulatory standards.
Individuals or organizations that handle controlled substances, such as pharmaceutical companies, laboratories, and healthcare providers, are required to file printable control logs.
To fill out printable control logs, one must input relevant information such as date, time, quantity of substances, purpose of use, and signatures of individuals involved in the transaction.
The purpose of printable control logs is to maintain accurate records of the acquisition, use, and disposition of controlled substances, thereby ensuring accountability and regulatory compliance.
Information that must be reported on printable control logs includes the date, quantity of substances handled, location, purpose of use, and identities of personnel involved in the process.
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