THE VIRTUAL TWIN EXPERIENCE FOR BIOPHARMACEUTICAL MANUFACTURING COMMISSIONING

Commissioning and qualification (C&Q) are essential in the manufacturing of biotechnology and pharmaceutical therapies. In the Life Sciences industry, mandatory C&Q processes ensure that the buildings and equipment involved in the manufacturing, processing, packaging, holding and storage of a therapeutic product are fit for their intended use and compliant with regulations from the relevant authorities such as Food and Drug Administration (FDA) and European Medicines Agency (EMA). 

Download this whitepaper now to find out more. 

    All information that you supply is protected by our Privacy Policy.
    In order to provide you with this free service, we may share your business information with companies whose content you choose to view on this website.
    By submitting your information you agree to our Terms of Use.
    Third party cookies may be placed, to serve more relevant ads when you browse the web.
    You can learn more about those ads here.