Insights On Outsourced Drug Development
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PBPK Modeling For Optimized Controlled Release Formulation Development
8/24/2023
Examine the benefits of controlled release, the application of PBPK modeling in controlled release formulation development, and how modified release products can be developed to deliver optimal patient outcomes.
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Powerfully Simple Digital PCR
7/18/2023
Evaluate the performance of an E. coli kit based on it's detection sensitivity, quantification accuracy, and replicate uniformity as it performed when tested on a Digital PCR System.
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Vaccines: An Overview Of This Life Saving Innovation
12/1/2022
Pharmaceutical manufacturing is highly regulated. Learn about what a vaccine is, how it works, the approval process, and how some vaccines can be fast-tracked through the entire process.
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Taste Masking 101: Optimize Taste And Improve Patient Outcomes
8/18/2022
Taste masking is integral for a drug product’s final formulation. It can serve to increase patient acceptability and adherence to a therapy, in turn bolstering regulatory acceptance and commercial potential.
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A Micronization Method Enabling The Formulation Of Biopharmaceuticals
6/29/2023
Micronization is key for increasing the loading efficiency and lowering the burst of microspheres. Applying lyophilization-based micronization methodology at a small scale helps to support challenging formulation development projects.
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Planning for Success: Supply Resiliency Strategies for Bench to Production
10/18/2023
Build scalable material sourcing strategies for R&D and early phases through to commercialization and learn how to accelerate the development process and ensure the scalability of your biologics.
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The Importance Of Recording Zero In The Digital Age
4/9/2024
Explore the value of negative results and how proper data management enables your digital maturity journey towards scientific advancement.
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Emulate Endorses The FDA Modernization Act Of 2021
5/10/2024
Learn why removing the mandate for animal testing would enable faster, more efficient, and more humane drug development, all while benefiting both patients and the pharmaceutical industry.
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Scaling Up Your Methods with USP <621> - Part 3: Software
9/22/2023
Learn how Empower Software addresses modifications to certain calculations and maintains relevant naming conventions and calculations to help customers update SOPs to prevent disruption to operations.
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Nanoparticle Engineering Addresses The Challenge Of Poor Aqueous Solubility
3/24/2023
As pharma companies aim to overcome development obstacles, it is important to incorporate GMP expertise alongside novel technologies that can enhance the properties of APIs and dosage forms.