Have Confidence in Your Data – As Biopharma Advances, So Must Our Data Integrity
Therapies are more complex, tailored and varied than ever and the associated amount of data is growing – which requires a new level of attention to detail.
Therapies are more complex, tailored and varied than ever and the associated amount of data is growing – which requires a new level of attention to detail.
Leveraging multiple external partners, a leading clinical-stage biotechnology company manufactures AAV viral vectors as part of its proprietary gene delivery platform.
Gain key insights on the value of using purpose-built software systems to streamline your critical manufacturing data management and product quality processes across internal and external networks.
IDBS announces the latest release of its Skyland PIMS® software, which seamlessly combines product, process, and patient data across the biopharma life cycle and supply chain, providing insights that accelerate process understanding and ensure product quality.
The current state of biopharma drug development is a barrier to the timely and cost-effective treatment of disease.
Skyland PIMS version 4.2 introduces new capabilities to accelerate biopharma development and manufacturing by eliminating barriers to data and expanding statistical analysis to further enhance monitoring of processes across modalities, including cell and gene therapies, small molecule, and other biologics.
It’s been a busy year so far. And we’re only at the start of April! Find out what we’ve been up to in this blog.
Book your meetings with IDBS and Scitara at the IOT & Smart Pharma Summit this year in San Diego, CA. We look forward to being back in person and virtually in 2022.
Novavax has more than a decade of experience contending with some of the world’s most devastating diseases, including seasonal influenza, RSV, Ebola, MERS, and SARS
Join us for a discussion on the benefits of microservice architecture and approaches for deploying and managing SaaS solutions utilizing microservice architecture in GxP regulated environments.
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