Accurate regulatory reporting in a life sciences organization is critical for compliance and overall sucess. Here’s how Insight and Power BI can help.
Keep ReadingIDMP was once again a hot topic at DIA’s 2019 Regulatory Submissions, Information and Document Management Forum. Here’s what we think about the regulations.
Keep ReadingThrough the Box Skills Beta program, Daelight discovered a number of benefits that make partnering with Box for ML solutions a no-brainer.
Keep ReadingA step-by-step manual can help facilitate a smooth IT integration during mergers and acquisitions. Here’s how to develop your M&A playbook.
Keep ReadingIntegrating systems post-deal requires a well thought-out integration roadmap. Here’s how to get started.
Keep ReadingDaelight attended the recent BoxWorks conference to learn more about what Box is doing within the Life Sciences industry.
Keep ReadingNo matter the details of your deal make sure you’ve taken a thorough inventory of your tech assets before you sign on the dotted line.
Keep ReadingPharmacovigilance (PV) inspections are increasingly challenging, whether in small start-ups with limited resources or in big pharma organizations with complex contractual arrangements and diverse products. From process and documentation to PV systems and tools, you must be ready to address detailed inspection requests from regulatory authorities across the globe.
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