Leveraging Data Management for Root Cause Identification in Critical Environments 3/29/2019

With the increasing employment of sophisitcated Data Management software, the collection and evaluation of multiple data has never been easier! However, managing such a large amount of information may represent a challenge, resulting in a potential obstacle to effective identification of the root cause of the environmental OOS associated deviation in reasonable time. In this webinar you will learn the best practices to effectively approach a complete investigation with the support of an Environmental Monitoring Data Management software, combining the traditional investigation methods with the enhanced capabilities of analysis provided by the software-based solution.

 

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Speaker

Maurizio Della Pietra

Global Data Management Specialist and Process Advisor, Particle Measuring Systems

Maurizio Della Pietra is the Global Data Management Specialist and Process Advisor for Particle Measuring Systems. In this role, he collaborates and consults with pharmaceutical companies and with developers of pharmaceutical equipment and isolation technologies for improving the sterility assurance on science-based strategies. His expertise includes QA processes, validation of equipment, utilities, facilities, computer systems, aseptic production processes, and statistical analysis of aseptic production processes. He has earned a Master's Degree in Physics.

Speaker

Anna Campanella (PhD)

Global Sterility Assurance & Advisor, Particle Measuring Systems

Anna Campanella (PhD) is the Global Sterility Assurance Advisor for Particle Measuring Systems. In this role, she uses her industry experience to collaborate and consult with pharmaceutical companies to develop and implement science-based strategies, principles of monitoring, and controlling and improving the chemical, physical, and microbiological state of various production processes. Anna has a diverse background in the Pharmaceutical field including a PhD in Molecular Medicine, expertise in QA&QC processes, validation of chemical and microbiological methods, validation of sterile production processes and experience in microbiological aspects of aseptic production processes.