Consultancy service

GLP activities

Kain signs a consultancy agreement with a global biopharmaceutical company in order to provide professional advise and guidance in the field of GLP equipmment validation. The agreement comprises the following activities; writing validation protocols, coordinating the validation and writing validation reports.

Implementation LC-MS/MS technology in Germany

For an environmental laboratory in Germany, a LC-MS/MS system was implemented and made operational. In addition& Weiterlesen »

Interim management

In May 2011 KAIN accepts an interim management assignment in a laboratory outside Europe. During this period KAIN ensures the daily operations and is able to implement a number of improvements. 

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