Christophe Cochet

After 20 years spent in pharmaceutical companies, especially in QC and Quality operations, I have created my own company as freelance pharmaceutical consultant. Based on this previous and long experience, I would like now to support pharmaceutical companies in reaching GMP requirements and improving their industrial performance as well.
The key activities I would like to develop are around the following topics :
– Building efficient Quality Management Systems, including CAPA & deviation system, continuous process monitoring, trend analysis, QC and batch release
– Building and implementing Data Integrity Strategies.
– Implementing IS Quality management Tools
– Preparing Regulatory Inspections (especially coaching)
– Resolving major or critical quality issues
Please do not hesitate to contact me