"As we're preparing for a phase transition into clinical phase 1 we would also like to align our manufacturing capabilities with current GMP regulations."

Our team at LFSCNC would initially propose to conduct a GAP analysis, to verify whether your company’s SOPs & processes meet current GMP regulations (US/EU). After identifying those gaps, LFSCNC then would suggest corrective actions as needed so that your company’s quality system would comply with current regulations.

 

Last but not least, LFSCNC can also assist you with executing the corrective actions, and update SOPs and processes in close collaboration with your company’s internal team.   

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