• 验证总结指南

BioPure Q-Clamp 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

验证总结指南 PDF - 469.6kb

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免责声明:您在此同意所提供的验证指南仅供个人使用,以协助验证指南中列出的产品鉴定。

您还同意,未经 WMFTS 事先同意,您不得复制、重新分发、传输、转让、出售、传播、出租、共享、出借、修改、改编、编辑验证指南或将其转交给任何其他方。