The client is a Switzerland based top pharmaceutical manufacturing company. The client approached Freyr with an intention to perform audit for its Active Pharmaceutical Ingredient (API) suppliers. Freyr assisted the client with audit for two of its API suppliers’ manufacturing facilities and procedures. The major challenge faced by the client was to understand and decode the current Good Manufacturing Process (cGMP) requirements as per the Swiss Medic.
Read through the case study to decode how Freyr executed the project within two weeks with quick turnaround time.
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