The MHRA and FDA will expect that product and sample storage areas meet the required storage conditions as specified. To confirm that temperature and humidity consistently meet these requirements, common industry practice is to perform a mapping validation. This is very often carried out as part of the IQ and OQ for a new piece of equipment, cold store or warehouse.
Validair can carry out this mapping validation for a client using the latest digital sensors we can record temperature and humidity readings at many locations over extended periods of time. The results can be presented in a number of different graphical or numerical forms.