Archives for January 28, 2013

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Freeman signs up Canadian distributor

By Gareth Macdonald

Freeman Technologies has signed a Canadian distribution deal for its powder flow analysis tech in a bid to win more QbD and PAT-focused Pharma customers.

EU to Further Align GMP, Process Validation Standards with ICH, FDA

By Zachary Brennan

The European Medicines Agency (EMA) is looking to integrate guidance from the International Conference on Harmonization (ICH) and US Food and Drug Administration (FDA) into the revisions of two annexes related to its process validation and good...

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US asks for exemption from EU API import laws

By Gareth Macdonald

The US wants exemption from new European Union import rules for active pharmaceutical ingredients (APIs) and says such status would cut manufacturers' admin and help prevent drug shortages.