Production OTC

We manufacture and package OTC products for the United States and Canada in compliance with pharmaceutical standards (21 CFR part 210/211 ; Guidelines on Good Manufacturing Practices published by Health Canada)
  Manufacturing and packaging of OTC pilot batches
  Stability study according to ICH Q1
  Manufacturing and packaging of OTC industrial batches
  Writing of master production files (Master Batch Records)
  Qualification of equipment used for OTC (QI / QO / QP)
  Validation of analysis methods according to ICH Q2
  Process validation

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