We provide an extensive range of services pertaining to clean room validation by our panel of expert professionals available with us.AMFA Climatech performs the HVAC validations as per ISO 14644, EU cGMP, US Federal Standard 209E, USFDA ,Schedule M (National Regulatory Body)
Validation is the overall expression for a sequence of activities in order to demonstrate and document that a specific product can be reliably manufactured by the designed processes, usually, depending on the complexity of today's pharmaceutical products, the manufacturer must ensure; "that products will be consistently of a quality appropriate to their intended use"
Validation is a proof that a process works and this must be done using scientific and statically principles. This is done to establish process capability and to confirm product acceptability
Documentation is the key to GMP compliance and traceability of all development, manufacturing and testing activities. Documentation provides the route for auditors to assess the overall quality of operations within a company and the final product.
AMFA Climatech carries out following tests to validate clean rooms/clean zones.
We provide annual maintainace contracts for all our customers. Presently we have 3500 TONS of AMC for air conditioning.
We providing routine maintenance services, pertaining to complaints as and when they occur in commercical/ Industrial Air conditioner and annual maintenance services. AMC services shall include providing all man power, labour, tools and tackles and replacement of defective spare parts including consumables. We undertake comprehensive & Non-comprehensive Services.
Our scope of work shall include routine maintenance services, annual maintenance services, On call AMC services.