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The Impact of UK Collaboration in Life Sciences
In this opinion piece, Jan Wauters discusses why collaboration in science is so important and what the Windsor Framework could mean for research in Europe.
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Bringing the Beauty of Dissolution to the World of Medical Devices
Products coated with a small amount of drug that releases over an extended period of time aren’t suitable for traditional dissolution testing. Therefore, novel drug delivery mechanisms and devices require a new approach to this regulated technique.
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The Role of Smart Technology in Mitigating the Risk of Human Error and Improving Productivity in Pharmaceutical Quality Control
In this article, discover the role HPLC plays in ensuring regulatory compliance and reliability of throughput, and how labs can automate to eliminate errors and build reliability into their processes.
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ChatGPT: It’s Not the End of the World as We Know It
In this op-ed article, Michael Kinch explains his optimism around ChatGPT which, in his words, centers around the possibility that we as a society might start to question "claims" and "truths" that we encounter daily.
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“A Second Chance at Life”: Can Gene Therapies Beat Rare Disease?
A revolutionary gene therapy has become a transformative treatment for children with metachromatic leukodystrophy (MLD). But substantial barriers to access for this groundbreaking therapy remain.
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An Introduction to Transfection, Transfection Protocol and Applications
In this article, we discuss the fundamentals of transfection, provide an overview of some of the commonly employed methods and a sample protocol. Finally, we consider some of the key applications of transfection.
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Cutting With CRISPR: Assessing Safety as Technology Moves Into the Clinic
The Nobel Prize winning CRISPR-Cas genome editing technology is being adopted for a wide variety of research applications. In this article, we will explore what these applications are and outline the progress of CRISPR methodologies in recent years, in addition to current bottlenecks in CRISPR research and how we can look to address them.
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Passage of the FDA Modernization Act Enables New Era for Preclinical Testing
The 11th-hour passage of The FDA Modernization Act gave a much-needed boost to the advocates of new alternative methods (NAMs) for preclinical testing. In this article, we take a look at why NAMs are needed and what the new legislation means for pharmaceutical companies.
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Global Regulators Embrace Collaborative Initiatives
Regulators are increasingly collaborating on a global scale, sharing expertise across regions for mutual benefit. In this article, Piety Rocha examines this upward trend.
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Embracing Data-Driven Modeling Approaches Into Biopharmaceutical Processing
This article explores new workflows using data-driven modeling to improve culture medium and new control algorithms allowing for better modulation within the bioprocess design space.
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