On-Demand Webinars
-
Breaking Barriers: Combining Cell Line Development Innovation With Improved Process Development Workflows To Streamline Path To FIH
10/16/2024
Explore how KBI Biopharma’s SUREtechnology Platform™, powered by Selexis®, accelerates the development of complex biologics from early stages to first-in-human (FIH) trials, focusing on both speed and quality.
-
Achieving Manufacturing Efficiency In OSD Manufacturing
10/16/2024
Gain expert insight into the importance of instrumented tablet presses in assessing formulation properties, the role of tablet cup configurations, and scalability parameters for successful product transfer.
-
The Road To Approval: Viral Clearance Strategies For Non-Enveloped Viral Vectors
10/10/2024
Know the differences between designing a viral clearance study for non-enveloped viral vectors versus those for mAbs or recombinant proteins, and learn how to identify and remove viral contaminants.
-
From Crisis To Confidence In Medical Writing: Ensuring Smooth Regulatory Submissions
10/8/2024
Explore some of the major challenges that medical writing submission specialists face today and present strategies that can consistently set the stage for success.
-
Full Speed Ahead: Accelerating Your CHO Bulk Harvest Testing Using Rapid Methods
10/3/2024
With advanced rapid methods that offer both speed and sensitivity, you can expedite your bulk harvest testing and detect adventitious viruses in half the time compared to conventional techniques.
-
Mastering The Art Of Developing A Successful Bispecific Antibody
10/3/2024
Learn innovative strategies to overcome the complexities of bispecific antibody development, from intelligent design to efficient purification techniques.
-
Expanding The OSD Toolbox
10/3/2024
This session is designed to provide practical solutions for enhancing bioavailability and scalability in pharmaceutical formulations.
-
Understanding Nitrosamines: Key Regulations And Best Practices
10/2/2024
Gain expert insights into nitrosamine regulations and discover practical strategies for ensuring compliance and safeguarding product safety.
-
Understanding FDA Calibration Requirements And Best Practices For Reducing Risks
10/2/2024
Become equipped with the tools and strategies needed to strengthen your calibration efforts and better position your organization for success in regulatory audits.
-
Extractables And Leachables: Setting Up Early For Success With Your CDMO
10/2/2024
Discover insights tailored specifically for drug product researchers and manufacturers, offering key knowledge on extractables, leachables, and effective implementation strategies.