Free Webinar Series: “Automated Reporting in Biotechnology and Pharma”
This is a free, 3-part webinar series on Automated Reporting in JMP® for engineers, scientists, and analysts in Pharmaceuticals and Biotechnology.
This series will feature Predictum software engineer, Ben Peachy Higdon, Curtis Monnig, Vice President, Chemistry, Manufacturing and Controls at January Therapeutics, and Yasmine Hajar, PhD, PEng, Systems Engineer at JMP®.
Session 1: Automating APRs, MPRs, and Reporting in Pharma
February 28 | 10am – 11am ET
Session 2: Collaboration and Knowledge Capture in Pharmaceutical Research & Problem Solving: CoBaseKRM and JMP Live
March 16 | 10am – 11am ET
Session 3: Validating JMP Automation Applications: Meet the Modern, JSL DevOps Team
March 23 | 10am – 11am ET
Build Better and Faster with Small Experimental Designs and Machine Learning
Today’s pace of innovation requires companies to accelerate building better products and progressing process development to bring critical or high-demand products to market. This webinar centers on Self-Validating Ensemble Modeling (SVEM), a new modeling technique to support these goals, resulting in a greater ability to advance products rapidly from conception to maturity in shorter timeframes.
Knowledge Repositories for Faster Problem Solving & Reduced Time-to-Market
Get to know how a knowledge management strategy combined with a knowledge repository solution geared to engineering and science teams enable faster problem solving and reduced time to market.
Converging DOEs and Machine Learning with Self-Validating Ensemble Modeling
In this talk, we’ll provide an overview of S-VEM as a new, advanced machine learning method, demonstrate a couple of use cases using our new S-VEM analytical product, and suggest how you can explore this method further.
Modernizing Development Practices for Applications that Use JSL
The presenters will demonstrate the key components of the updated development environment and how they work together to boost the team’s daily work.
Facilitating CMC Development and Regulatory Filings with Phase-Appropriate QbD
Phase-Appropriate Quality by Design (QbD) is a systems approach to drug development and manufacturing that mitigates risk and facilitates regulatory compliance and successful outcomes. In this session, we will give an overview of our strategy for applying phase-appropriate QbD from early process development to commercialization to increase the rates of success. Learn the role of predictive modeling in enhancing QbD and new methods that it employs.
Enhancing and Extending JMP’s Process Screening Platform
This talk will explore the JMP Add-In, its use and advantages from our client KLA’s perspective, as well as its design and implementation insights from the development viewpoint.
JMP Discovery Summit Americas 2022 (online)
September 12-14, 2022
SAS world headquarters
Cary, North Carolina
September 19-21, 2022
JMP Discovery Summit Europe 2023
March 2023 (dates and times TBA)
JMP Discovery Summit Europe 2022 (online)
March 8, 10, 22 and 24, 2022
JMP Discovery Summit Americas 2021 (online)
October 4-8, 2021
JMP Discovery Summit Europe 2021 (online)
March 8-12, 2021
JMP Discovery Summit Americas 2020 (online)
October 12-16, 2020
JMP Discovery Summit Munich 2020 (online)
March 10-12, 2020
JMP Discovery Summit Americas 2019
October 15-18, 2019