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hi everyone i am udaishati and youre watching another session of pharma best practices webinars the topic for todays webinar is cleaning validation regulatory guidelines for the pharmaceutical industry todays session is the 68th session of pharma best practices webinar series information about all webinars is available on our website pbpw dot in the website is pbpw dot in we have several webinars platinum planned in the next three months you can register for these webinars on the website you can also watch recordings of past webinars and you can join pharma best practices forum on this website these are chat groups to discuss technical subjects let me now say a few words about todays topic for the webinar which is cleaning validation in non-sterile pharmaceutical manufacturing which is moving towards a risk-based approach this is a docHub change in all aspects for the industry in this presentation thomas altman will summarize the global regulatory guidelines leading to all the