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ACD/Labs Blog

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How Chemical Manufacturing and Control (CMC) Software Helped a Major Pharmaceutical Company Improve Process Development and Regulatory Submissions Background: In 2019, a process development team at a top biopharmaceutical company felt data management was getting in the way of research and that too much time was spent preparing regulatory submissions. Challenge: The team wanted to...

Joel Michalski
Biopharmaceuticals have boomed in recent years, with innovative researchers transforming complex biomolecules into effective therapeutics. Unfortunately, many of the common applications used by scientists do not meet the needs of this rapidly expanding R&D sector. Researchers need a chemically intelligent platform that understands the structure and properties of biochemical molecules. A vendor-neutral informatics environment will...

Jesse Harris
The rapid increase in biopharmaceutical approvals and sales indicates their tremendous opportunities in the coming years. Innovative software solutions play an essential role in unlocking that potential. Learn more about how ACD/Labs brings chemical intelligence to biopharmaceutical research in this blog post.

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Critically Examining Data Management in ADC Development and Research Antibody Drug Conjugates (ADCs) are a class of therapeutics that utilizes the specificity of monoclonal antibody (mAB) to enable targeted drug delivery. With more than 180 ADCs currently in clinical trials, the ADC market is predicted to grow from $2-3 billion today to over $13 billion...

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E&L contains large amount of analytical datasets and chemical information of all impurities associated to each study. Luminata’s ability to be configurable allows it to handle each step within the extractable and leachable process, to store all meta data for each compound found in the study with its corresponding data.

Joel Michalski
In this webinar we discuss how you can manage all your theoretical and observed degradants, experimental conditions, and analytical results (including LC/MS data and structural information) using our software solution, Luminata®.

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How evolving analytical and automation tools are positively impacting forced degradation studies in pharmaceutical development The goal of stress testing or forced degradation in pharmaceutical development is to comprehensively compile relevant degradation pathways, such that all degradation products are formed at detectable levels. This field has grown significantly in the past 20 years, fueled in...