Very interesting round table from the Interphex on podular systems.

https://www.youtube.com/attribution_link?a=lk7--sJ-qrM&u=%2Fwatch%3Fv%3DoAv5wU918lM%26feature%3Dshare

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There are still some out there, which believe in paper instead of testing. Robust proof of filter performance testing, at least firm evaluations, whether sterilizing grade or not, shall prevail over paper. It is stated; by just specifying the use of a sterilizing grade filter, the end-user gets by with a paper-based risk assessment and no validation whatsoever. One specifies a sterilizing grade filter, one has to validate it as such and it does not matter whether the buffer needs to be sterile or not. A performance claim is made, you have to proof it. See PDA TR 26, FDA 2004.

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And another interesting single-use technology maneuver.

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With great honor and gratitude, I received the prestigious Martin Van Trieste Pharmaceutical Science Award during yesterday's PDA awards dinner. I feel humbled to be recognized by my professional industry peers, colleagues and friends.

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Just very few more registration slot available. Sign-up soon to join an expert group discussing aging facility, processes and analytics problems and solutions to overcome such problems.

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G-CON Manufacturing is exhibiting at Interphex 2015 in New York City, and we invite you to join us for this important industry event. Come see us and learn more about G-CON Manufacturing and meet the people behind our products. We will be in Booth #2421, showcasing our autonomous cleanroom PODs.

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Join us to discuss this extremely important topic and the improvement options ! The agenda and quality of topics for this workshop are excellent !

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Join us in face-to-face discussions and case study analysis.

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