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BURDEN TESTING SAMPLE SUBMISSION FORM (DEVICES & PROCEDURAL PACKS)Date: Client Information Purchase Order (if available):Company Name:Quotation No (Mandatory for proper registration of samples): URGENT
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How to fill out bioburden testing sample submission

01
Collect the samples using aseptic techniques.
02
Place the samples in sterile containers to prevent contamination.
03
Label each container with the necessary information such as sample ID, date, and location.
04
Fill out the submission form with all required details including sample ID, type of sample, date collected, and any other relevant information.
05
Package the samples securely to prevent any damage during transportation.
06
Send the samples to the designated testing facility along with the submission form.

Who needs bioburden testing sample submission?

01
Bioburden testing sample submission is needed by manufacturers of medical devices, pharmaceutical companies, and other industries where contamination control is crucial.
02
Regulatory bodies may also require bioburden testing sample submission to ensure compliance with quality standards.
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Bioburden testing sample submission refers to the process of sending samples of a product to a laboratory for analysis of the microbial load present, typically to determine the number of viable microorganisms.
Manufacturers of sterile products, pharmaceutical companies, and any entities that produce products intended for use in sterile environments are typically required to file bioburden testing sample submissions.
To fill out a bioburden testing sample submission, the submitter needs to provide details such as the product description, batch/lot number, sampling date, and any relevant specifications or testing methods requested by the laboratory.
The purpose of bioburden testing sample submission is to assess the microbial quality of products before they are released for further processing or for sale, ensuring they meet safety and quality standards.
The information that must be reported includes the product name, batch number, sample collection date, type of test requested, and any specific guidelines or previous test results relevant for the assessment.
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