Sterility PT

NA.24

Sterility proficiency testing material is produced in accordance with ISO/IEC 17043:2010. The PT portfolio allows our test components to offer significant performance data to monitor and prove competency to customers, accreditation bodies or both.

Supelco^® Pharmaceutical Proficiency Testing scheme is mainly designed to meet the needs of the pharmaceutical industry.
The pharma PT samples allow laboratories to demonstrate their competence in following compendial USP methods of analysis. They can be used to assure accreditors or auditors that the lab processes are followed accordingly. Our pharmaceutical PT scheme covers products under categories such as Chemical Tests and Assays, Physical Tests and Determinations and Microbiological Tests.

Type of PT Scheme: Pharmaceuticals

All information regarding the use of Sterility proficiency testing standard can be found in the reporting packet which will be available to download at PT Portal.

Sterility pharmaceutical proficiency testing material is used in the pharmaceutical analysis for any microbial growth identification.

Have any questions? Explore ourFAQs.
For more information on this product, please contact our PT Service Team.

We have a vast portfolio of environmental PT schemes with "fit-for-purpose" samples to help you meet the needs of the laboratory.

Our proficiency testing (PT) program is a benchmark to:

• provide staff with an insight into their laboratory′s performance, to verify the accuracy and reliability of their testing process
• provide a comparison of performance with that of other laboratories, nationally and internationally
• test and educate staff, provide a better understanding of the impact of incorrect results and identify areas where there may be problems
• provide an independent evaluation of laboratory performance
• demonstrate to clients, colleagues and accreditation bodies that there is a commitment to quality

Description

• The sample is a vial containing a small Vitroid^™ (media containing possible organisms). It is the colored disk on top of the cotton ball. The yellow beads are desiccant.
• Each sample may be presented with a unique cap color to help distinguish between the different material batches provided:

Sample 1 - Clear Cap
Sample 2 - Red Cap
Sample 3 - Blue Cap

Sample Preparation

• Allow the vial to warm to room temperature.
• Transfer the colored tablet to buffer water and let sit for 15 min, the tablet will slowly dissolve. After 15 min gently shake the sample until the tablet dissolves completely. You may also use your media to hydrate. It is suggested to use no more than 100 mL for hydration. If 100 mL is used a minimum sampling size is no less than 1 mL.
• This is to be considered your sample for test. This sample may be diluted up to 1:5.
• Further dilution may dilute out the organisms.

Reporting Instructions

• If growth occurs report ′1′.
• If no growth occurs report ′0′.
• Contact ptservice@milliporesigma.com if you have any questions or if you have an unexpected result.

Are you new to Supelco^® Proficiency Testing? Be sure to register your account details in the PT Portal before placing your order.
This will provide access to data entry, reporting packets and final reports. Registrations will be approved shortly after your order is placed. For further questions, write to us at ptservice@milliporesigma.com.

When placing your order online, please indicate your study preference under the ′your reference′ column. Available studies can be viewed at the bottom of the page.
Click here to learn more about Quick-Turn Studies (on-demand proficiency tests that are offered depending on lot availability). The Quick-Turn results are released within 48-72 hours whereas scheduled study reports are released within 21 days.

Proficiency Testing Schedule (2021-2022)

Pharma
PHARM21-4 October 6 - November 19, 2021

PHARM22-2 April 6 - May 20, 2022

Supelco is a registered trademark of Merck KGaA, Darmstadt, Germany
Vitroid is a trademark of sigma-aldrich Co. LLC

100

pkg of 3 × 1 ea

suitable for (suitable for 71 per USP)

pharmaceutical

matrix material

Please refer to sample label for expiration date, specific storage temperature, and specific storage conditions.

6.2 - Infectious substances

WGK 1