LCV Pharma writes and execute pharmaceutical protocols.

 

From the existing pharmaceutical facilities to the newly constructed facilities, LCV Pharma writes and execute
protocols, such as:

• User Requirements, Functional and Design Specifications for Automation Projects (URS, FS, DS);
• Tests procedures elaboration based on Risk Analysis (TP, FRA, RTM)
• Control System Validation (FAT, IQ, OQ);
• Protocols are written using the latest guidelines from the GAMP 4 and the 21 CFR Part 11;