• Validation summary guide

BioPure Q-Clamp validation summary guide

Find out more about the validation summary guide.

Validation - Q-Clamp sanitary Tri-clamp

Q-Clamp is supported by an industry leading validation package for non-wetted components and meets current industry requirements including ISO 10993: Parts 5, 6, 10, and 11, USP <88> & USP <87>.

  • Suitable for sterilisation by autoclave or gamma irradiation
  • Lot traceable from material to final product
  • Pressure rated up to 7 bar
  • Manufactured and packed in an ISO Class 7 cleanroom

Additional testing carried out includes extractables testing.

The full validation guide including additional information regarding test methods and actual test reports is available on request.

Q-Clamp, its raw materials and manufacturing process meets a number of regulatory compliance legislations. Specific statements relating to these compliances are available in the Q-Clamp compliance guide.

Both the full validation guide and the compliance guide can be requested by submitting the below form.

 

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BioPure Q-Clamp validation summary guide

Validation summary guide PDF - 469.6kb

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Disclaimer: You hereby agree the provided validation guide is for private use only to assist in the qualification of the products listed within the validation guide.

You also agree that you will not copy, redistribute, transmit, assign, sell, broadcast, rent, share, lend, modify, adapt, edit or transfer the validation guide to any other party without prior consent from WMFTS.