Experts will discuss regulatory requirements, best practices, and process security for data integrity at INTERPHEX 2018.
Pharmaceutical Technology will present the INTERPHEX Keynote Series: Data Integrity on Wednesday, April 18, 2018 on the show floor at the Innovation Stage, open to all show attendees.
Regulatory Requirements for Data Integrity, Applying ALCOA+: 11–11:30 am
Data integrity is crucial for both the pharmaceutical laboratory and the manufacturing floor. What is data integrity? How can a company ensure data integrity throughout their processes and facilities? Els Poff, Executive Director, Data Integrity Center of Excellence, Merck, representing the PDA Data Integrity Task Force, will answer these questions and more.
Click here to register for INTERPHEX.
Best Practices in Data Integrity and Process Security with Automated Systems: 11:30 am–12:30 pm
A panel of industry experts will discuss how to ensure data integrity with manufacturing automation systems, as well as cybersecurity, best practices for auditing system security, and security concerns associated with the Industrial Internet of Things. Panelists are: Bob Lenich, Global Life Sciences director, Emerson; Torsten Winkler, lead of the Life Sciences Center of Excellence in EMEA for Honeywell Process Solutions; Bob Mehta, Principal Consultant, MasterControl through GMP ISO Expert Services; Mark Cristiano, Manager, North America Business Development Team, Connected Services and Solutions, Rockwell Automation; and Nicolas Teissié, Siemens Industry Software Product Manager.
Clinical Supply Planning in Europe - Balancing Cost, Flexibility and Time
December 19th 2024The packaging and distribution of clinical supplies is a fundamental piece to the overall success of a clinical trial, and advance preparation can help establish a more efficient supply chain. Selecting the best geographical location for those activities, however, depends on the clinical trial protocol, business decisions, and even the investigational medicinal product (IMP) being studied.