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This document outlines the specific procedures for the collection, processing, and storage of laboratory specimens from participants enrolled in the Women's Interagency HIV Study (WIHS). It includes
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How to fill out womens interagency hiv study
How to fill out Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures
01
Prepare all necessary materials and equipment before starting the specimen collection.
02
Ensure that you have the appropriate types of laboratory specimens required for the study, such as blood, urine, or tissue samples.
03
Follow the guidelines for identifying the participant and labeling specimens correctly to avoid mix-ups.
04
Use aseptic techniques when collecting blood or other specimens to prevent contamination.
05
Collect samples according to the specified methods in the protocol, ensuring that volumes and handling procedures are adhered to.
06
Document the time and conditions of specimen collection, including any relevant clinical data.
07
Store specimens at the required temperature and conditions immediately after collection.
08
Process specimens in accordance with the laboratory protocols outlined in the study, including centrifugation, aliquoting, and freezing or refrigerating as necessary.
09
Complete any required paperwork associated with specimen tracking and analysis.
Who needs Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
01
Research personnel conducting the Women's Interagency HIV Study.
02
Laboratory staff responsible for processing and analyzing specimens.
03
Clinical teams involved in participant recruitment and care within the study.
04
Data administrators needing to maintain accurate records for compliance and reporting.
05
Regulatory bodies requiring adherence to established laboratory specimen handling protocols.
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People Also Ask about
What is Plhiv in HIV?
Over the years of coping with the stigma and discrimination that accompany the diagnosis in most societies, a large number of support groups have been formed. In these groups, the term most often applied to people who are HIV-positive is "People Living With HIV/AIDS". This is often abbreviated as "PLWHA" or "PLHIV".
What is Johns Hopkins HIV women's Health Program?
For over 30 years, the Johns Hopkins HIV Women's Health Program has provided comprehensive health care to women living with HIV/AIDS. Our experts offer a variety of services including gynecologic, obstetrical and preventative care, community outreach and linkage to other services.
What is the women's interagency HIV study?
The Women's Interagency HIV Study (WIHS) was a multicenter longitudinal study to investigate the progression of HIV disease in women. The WIHS started in 1993 in response to growing concern for the impact of HIV in women.
What is the specimen collection for HIV?
Blood (serum, plasma, DBS) is the preferred specimen for testing because it has a higher concentration of HIV antibodies than oral fluid. It also allows for additional testing, including for syphilis, hepatitis B and hepatitis C, and for special studies of HIV type and subtype, and ARV resistance.
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What is Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
Women's Interagency HIV Study - Section 10 outlines the protocols and guidelines to ensure proper collection, handling, and processing of laboratory specimens to support research on HIV among women.
Who is required to file Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
Researchers, laboratory personnel, and clinical staff involved in the collection and processing of specimens for the Women's Interagency HIV Study are required to adhere to these procedures.
How to fill out Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
To fill out Section 10, staff should follow specific instructions provided within the document, ensuring that all required fields are completed accurately, including sample identification, collection date, and processing details.
What is the purpose of Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
The purpose is to standardize specimen collection and processing methods to enhance the reliability of research data and ensure compliance with regulatory standards for HIV-related studies.
What information must be reported on Women's Interagency HIV Study - Section 10: Laboratory Specimen Collection and Processing Procedures?
Key information includes participant identifiers, specimen types, collection and processing dates, storage conditions, and any deviations from the standard procedures.
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