Blog
How Modern Teams Ace Regulatory Submissions: From Fragmentation to Flow
If you work in pharma or biotech, you know that accurate, complete, and well-coordinated regulatory submissions are critical to keeping development timelines on track. Every ...
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How Process Automation and AI Minimize Human Error in the Drug Development Lifecycle
Picture this: A global medical device manufacturer misses a small but crucial update to its product labeling in Europe. The result? A product recall, millions ...
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AI in Life Sciences: Transforming Clinical and Regulatory Workflows
Pharma and biotech leaders today are under immense pressure. You’re asked to accelerate trial timelines, cut costs, and stay compliant with constantly evolving regulations; all ...
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Shortcast Episode 9: Smarter Site Selection with Process Automation
Selecting the right sites is one of the most critical and challenging steps in clinical trials. Yet, many sponsor organizations still rely on outdated processes, ...
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Shortcast Episode 8: How are leading pharma companies modernizing their labs?
Pharma labs are under constant pressure to do more—faster. But with rising sample volumes, complex experiments, and rigid Laboratory Information Management Systems (LIMS), many labs ...
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Shortcast Episode 7: Simplifying Global Label Management
How do global pharma companies ensure every product label remains accurate, compliant, and up to date across dozens of markets? Behind the scenes, label management ...
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Bridging the Legacy Gap: How Data Fabric Powers Life Sciences Integration
Key Topics Covered: The Legacy System Dilemma in Life Sciences What is Data Fabric? And Why It Matters? Life Sciences Use Cases for Data Fabric ...
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Shortcast Episode 6: What is Low-code Process Automation?
As the pace of drug discovery accelerates, the organizations that thrive will be those that can adapt quickly. Traditional, siloed systems often make it difficult ...
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Smarter Site Selection in Clinical Trials: where Process Automation meets AI
A New Era for Feasibility in Clinical Research In the high-stakes world of pharma R&D, selecting the right clinical trial sites is both critical and ...
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Shortcast Episode 5: How is RPA different from Workflow Automation?
Process Automation in life sciences is no longer a question of if, it is a question of how. Among the many approaches, two terms often ...
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Shortcast Episode 4: Navigating EU-CTR Compliance with Workflow Automation
The European Union Clinical Trial Regulation (EU-CTR) was designed to bring consistency and transparency to how trials are assessed across Europe. For sponsors, however, ...
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Smarter Regulatory Submissions, powered by Process Automation and AI
Life Sciences is one of the most highly regulated industries, given its impact on human health. Organizations must comply with complex regulations throughout the lifecycle ...
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Shortcast Episode 3: How does Process Automation Streamline Regulatory Submissions?
Regulatory submissions are one of the most complex, time-sensitive and critical parts of the drug development process. Spanning multiple countries and many regulatory authorities, ...
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