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.

Date: March 29, 2019

Register: 11:00am Eastern Time

 

Speaker

Maurizio Della Pietra

Global Data Management Specialist and Process Advisor Life Sciences Division

Maurizio 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 experience in the pharmaceutical field includes computer system validation and compliance; Validation and Sterility Assurance; freeze-dried and liquid sterile drug products derived from human plasma. His expertise includes QA processes, validation of equipment, utilities, facilities, computer systems, data and production processes aseptic production processes and statistical analysis of them. He earned his Master's Degree in Physics.

Speaker

Anna Campanella

Global Sterility Assurance & Advisor, Life Sciences Division

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.

 

Moderator

Daniele Pandolfi

Life Science Division, Global Product Line Manager, Aerosol, Particle Measuring Systems

Daniele Pandolfi is the Global Product Line Manager, Aerosol in Particle Measuring Systems' Life Science Division. He has over eleven years' experience in particle counter instrumentation and cleanroom contamination control, focusing on strong customer relationships. He has helped many cleanroom users solve their cGMP issues. Mr. Pandolfi has been responsible for the EMEA Service Department, and a member of the of the Global Life Science organization in 2015.