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This document serves as an application form for laboratories wishing to participate in the California Blood Lead Proficiency Assurance Program, detailing the necessary information and contact details
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How to fill out application for participation in

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How to fill out APPLICATION FOR PARTICIPATION IN THE CALIFORNIA BLOOD LEAD PROFICIENCY ASSURANCE PROGRAM

01
Obtain the APPLICATION FOR PARTICIPATION IN THE CALIFORNIA BLOOD LEAD PROFICIENCY ASSURANCE PROGRAM form from the official website or relevant authority.
02
Fill in the applicant's name and contact information accurately.
03
Provide the name and address of the laboratory that will be participating in the program.
04
Indicate the type of laboratory (e.g., clinical, research, etc.) and any relevant accreditations.
05
Complete all required sections regarding the laboratory's current testing capabilities and methodologies.
06
Sign the application form certifying that all information provided is true and complete.
07
Submit the application form to the designated authority via mail or electronic submission, as instructed.

Who needs APPLICATION FOR PARTICIPATION IN THE CALIFORNIA BLOOD LEAD PROFICIENCY ASSURANCE PROGRAM?

01
Laboratories involved in blood lead testing that seek to ensure competency and compliance with California's proficiency standards.
02
Public health agencies requiring validation of laboratory testing results for lead exposure.
03
Researchers and medical facilities conducting studies or treatments related to lead exposure.
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People Also Ask about

Some of the documents below refer to a blood lead level of 5 micrograms per deciliter (μg/dL) as the CDC's blood lead reference value. CDC uses a blood lead reference value of 3.5 micrograms per deciliter (µg/dL) to identify children with blood lead levels that are higher than most children's levels.
Information for California Health Care Providers ​​The new CDC BLRV at which healthcare providers are recommended to provide follow-up is 3.5 mcg/dL, and CDPH encourages healthcare providers to provide retesting and follow-up for blood lead levels ≥ 3.5 mcg/dL.
Airborne Lead Dust Exposure Limits The revised California lead standard lowered the state's Permissible Exposure Limit (PEL) from 50 micrograms of lead per cubic meter of air (50 µg/mg3) to 10 µg/mg3 as an eight-hour time-weighted average (8-hr TWA) and its Action Level (AL) from 30 µg/mg3 to 2 µg/mg3 as an 8-hr TWA.
The calculated IRLs are 2.2 micrograms (µg) per day for children and 8.8 µg per day for females of childbearing age.
Information for California Health Care Providers ​​The new CDC BLRV at which healthcare providers are recommended to provide follow-up is 3.5 mcg/dL, and CDPH encourages healthcare providers to provide retesting and follow-up for blood lead levels ≥ 3.5 mcg/dL.
​​Definition of "Lead-Contaminated Dust" - UPDATED The new definition found at Title 17 of the CCR Section 35035 lowers the standard for interior floor surfaces from 40 micrograms (µg) of lead in dust per square foot (ft2) to 10 µg/ft2, and for interior horizontal surfaces from 250 µg/ft2 to 100 µg/ft2.
Apply to the California Department of Public Health for your Lead Sampling Technician certification using form CDPH 8488 (View Application). Include the required photos, documentation, and certification fee of $75 with your application. All fees are non-refundable.
You can determine your eligibility for each of the types of certification by reviewing the eligibility page. If you have further questions about your eligibility, you can contact CDPH at 1-800-597-LEAD(5323) (outside California: 510-620-5694).

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The APPLICATION FOR PARTICIPATION IN THE CALIFORNIA BLOOD LEAD PROFICIENCY ASSURANCE PROGRAM is a form that laboratories must complete to demonstrate their proficiency in testing blood lead levels and ensure compliance with California's health and safety standards.
All clinical laboratories in California that perform blood lead level testing are required to file this application to participate in the proficiency assurance program.
To fill out the APPLICATION FOR PARTICIPATION, laboratories must provide accurate information regarding their testing procedures, staff qualifications, and quality control measures, and submit the completed form according to the state's guidelines.
The purpose of this application is to ensure that laboratories are capable of accurately testing for lead levels in blood and to maintain public health standards by ensuring reliable and consistent testing across the state.
The application must report information including laboratory identification details, testing methodologies, personnel qualifications, quality assurance practices, and any relevant data necessary to evaluate the laboratory's proficiency in blood lead testing.
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