In today's pharmaceutical manufacturing industry, there are major challenges with getting the data you need from all the disparate sources and paper records across the organization in order to make business decisions. Then when you get the data, it requires error-prone manual work to analyze and generate reports. Working in spreadsheets, dealing with the delay of getting the additional data needed and using un-validated analysis results and reports are all major problems that people face every day. This costs organizations time, resources and ultimately, money.
Join us for this live webinar and learn how The BIOVIA Biologics Manufacturing solution has already helped many top 100 pharma companies reduce variability and batch failures in their biologics production process. These companies were struggling with data access and bioprocess understanding and needed to implement a solution to understand the sources of variability and monitor their processes with automated alerts and review-by-exception. Within a few months of implementing the BIOVIA Biologics Manufacturing solution, users report reduced data aggregation times and improved bottom line as a result of fewer batch failures and reduce batch processing time.
Register for this webinar to learn how your organization can benefit from the BIOVIA Biologics Manufacturing solution, including:
- Identify Critical Process Parameters (CPP) and operating ranges required for sustainable bioproduction process and product quality (Critical Quality Attributes - CQA) at commercial scale
- Establish a culture of data for bioprocess knowledge sharing and collaboration
- Maximize productivity and minimize costs with automated alerts and monitoring-by-exception
- Enhance process improvement by understanding and controlling bioprocess and product variability
- Reduce costs of deviations with near real-time data access and advanced analytics
- And much more
Larry R. Fiegland, Ph.D.
Lead Field Application Scientist
As a Lead Field Application Scientist, Larry has been part of the Product Development organization within BIOVIA since 2012 and is responsible for pre-sales activities, implementation support, and product development for the BIOVIA Discoverant solution. Larry obtained his Ph.D. from Virginia Tech under the direction of Professor John R. Morris, working on ultrahigh vacuum studies of the reaction mechanisms of ozone with saturated and unsaturated self-assembled monolayers. Prior to graduate school, Larry's industrial experience includes four years as a New Process and Development Chemist working on scale up of chemical processes from pilot plant to full scale manufacturing.
Daniela Jansen, Ph.D.
Sr. Product Marketing Manager
Dr. Daniela Jansen is a Sr. Product Marketing Manager at BIOVIA and has more than 20 years of experience in laboratory informatics and instrumentation holding various positions in Marketing and Sales Management. She is working on the strategic product positioning and customer benefits of the BIOVIA Life Science solutions and has expertise in 21 CFR Part 11 Compliance and Lean Six Sigma.
- Improving process outcomes by identifying sources of process variability for improved process control
- Improving process performance visibility with automated trending and alerts for review-by-exception to enable preemptive action
- Providing on-demand data access, aggregation and contextualization to reduce non-value-adding manual tasks and the risk of errors
- Role-based signal monitoring dashboards for process performance visibility across the production
- Chief Operating Officer
- VP/Director/Manager of IT
- Quality Engineer
- VP/Director/Manager of Manufacturing
- Scientist
- Applications Specialist
- VP/Director/Manager of Quality
- VP/Director/Manager of Operations
- Lab Manager
- Lab Analyst
- VP/Director/Manager Regulatory
