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Questions and answers on implementation of risk-basedprevention of cross-contamination in production and‘Guideline on setting health-based exposure limits for usein risk identification in the manufacture of differentmedicinal products in shared facilities’(EMA/CHMP/CVMP/SWP/169430/2012)
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Summary
This questions and answers document is currently being revised following the comments received during the public consultation and the workshop hosted by EMA on generation and use of Health Based Exposure Limits (HBEL), on 20-21 June 2017. In the meantime manufacturers should apply the Health Based Exposure Limits guide to all products and assess/control risk based on this data.
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