2. Incubation methods: For storage and stability testing of finished, intermediate products, and raw material samples temperature and humidity controlled rooms are required. Regarding microbiological testing, incubators for sterility tests and devices for studies concerning viable counts and “media fill” units are utilised. For cold and freeze rooms, as well as for incubators and stability chambers, documented evidence for suitability of the methods is required. Valicare offers GMP compliant qualification and validation of the equipment and the incubating process, including temperature distribution, determination of cold and hot spots, and checks for temperature stability by "temperature mapping". Our services include: