In a process known as qualification and validation, regulatory agencies such as FDA, EMA and WHO, require that the pharmaceutical, medical device and supply chain industries prepare documents that prove the proper functioning of processes, systems, and equipment. Traditionally, qualification and validation are documented on paper, then filed in binders or folders. Some companies use a set of electronic systems to cover all validation lifecycle documents. In this webinar, experts discuss the advantages of automated processes and remote, digital processing and validation in the context of COVID. Access the full webinar here.
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