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LSNE Passes FDA Inspection

Lyophilization Services of New England, Inc. (LSNE) has recently completed a comprehensive FDA audit of its medical device manufacturing facility in Manchester, NH.

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By: Tim Wright

Editor-in-Chief, Contract Pharma

LSNE has recently completed a comprehensive FDA audit of its medical device manufacturing facility in Manchester, NH. The successful completion of the week-long audit, for which no 483 citations were issued, demonstrated a quality cGMP manufacturing environment for services offered.

LSNE also recently completed an FDA Pre-Approval Inspection (PAI) and Compliance Audit for an Abbreviated New Drug Application (ANDA) for a sterile-injectable drug product at its Bedford, NH fill/finish facility.


Click here to learn more about LSNE

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