Validation of HVAC air conditioning systems for clean rooms, grade A/B, B, C, D;
Validation of air conditioning processes for storage facilities specific to pharmaceutical products (pharmacies, air-conditioned warehouses, cold rooms 2…8°C, transportation vehicles) according to GDP for pharmaceutical products.
Validation of Purified/Distiled Water Systems
Validation of Instrument Air Systems
Computerized Systems Validation
Validation documentation consist of:
Documentation (protocols/reports), including verification tests;
Completion of documentation with the results
obtained after testing and the resolution regarding the system validation activities.
Documentation and the neccesary technical support
for creating the operating procedures for temperature and humidity monitoring system;