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MQP – 014 EQA HANDBOOK EDITION 6 A participant ... - Thistle QA

MQP – 014 EQA HANDBOOK EDITION 6 A participant ... - Thistle QA

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Clinical Microbiology<br />

Pregnancy<br />

ESR<br />

April & October<br />

P.O. Box 131375, Bryanston, 2074<br />

Ground Floor, Block 5<br />

Bryanston Gate, 170 Curzon Road<br />

Bryanston, Johannesburg, South Africa<br />

804 Flatrock, Buiten Street, Cape Town, 8001<br />

www.thistle.co.za<br />

Tel: +27 (011) 463 3260<br />

Fax: +27 (011) 463 3036<br />

Fax to Email: + 27 (0) 86-557-2232<br />

e-­‐mail : service@thistle.co.za<br />

<strong>MQP</strong>-­‐<strong>014</strong><br />

Edition 10<br />

Food Micro<br />

May & November<br />

Infectious Disease<br />

June & December<br />

How do the <strong>E<strong>QA</strong></strong>s operate<br />

Provided you have enrolled timeously, your kit will be dispatched approximately<br />

2 weeks before the start date of the new cycle. Bear in mind that samples are<br />

imported and there may at times be customs issues which we do not have<br />

control over, but we will however endeavour at all times to get the samples out<br />

to you on time. Your kit usually has enough samples to cover a six month period.<br />

With the kit comes an instruction sheet, method questionnaire and results entry<br />

sheet for you to fill in.<br />

This results entry sheet already has your own unique <strong>QA</strong> Number on it.<br />

Please choose the method of your choice for each analyte listed on the method<br />

questionnaire and return together with your results to enable correct<br />

registration.<br />

In addition, we send you a Participation Certificate.<br />

The instruction sheet has lots of important information and it must be read<br />

carefully. For example,<br />

Ø Dates of analysis, or the final date by which we must receive your results.<br />

Ø Safety and disposal details for handling the sample<br />

Ø Reconstitution or mixing details<br />

Ø The important recommendation that you analyse our samples exactly as if<br />

they were patient samples<br />

Ø Storage details<br />

Ø Factors that could affect the testing if applicable<br />

Ø Environmental conditions<br />

Ø Recording and reporting of results<br />

Ø Contact details for any enquiries<br />

Ø Return policy of samples when applicable<br />

Page 5 of 12

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