Posts Tagged ‘Qualification/Validation’






Requalification – GMP-requirements for the pharmaceutical industry are valid worldwide

The initial achieved qualification status has to be maintained durably. For this purpose, relevant influencing factors on General Manufacturing Process (GMP) have to be checked periodically. The regulatory requirement of requalification is mandatory worldwide. Prominent superordinate regulations are the GMP guidelines of the US and the EU as well as the guidelines of PIC/S. …more



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Dear visitor,

6,100 employees, up to 150 years of experience, one thing is new: our name!
From now on we are called: Syntegon

Our website can be reached in the future at: www.syntegon.com
What is behind Syntegon? The numbers speak for themselves: www.syntegon.com/numbers

Your Syntegon Team
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