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The 2019 Veeva Summit provided a valuable opportunity to learn about the latest developments in the Life Sciences space – and we were very impressed.

Accurate regulatory reporting in a life sciences organization is critical for compliance and overall sucess. Here’s how Insight and Power BI can help.

IDMP 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.

Through the Box Skills Beta program, Daelight discovered a number of benefits that make partnering with Box for ML solutions a no-brainer.

A step-by-step manual can help facilitate a smooth IT integration during mergers and acquisitions. Here’s how to develop your M&A playbook.

Integrating systems post-deal requires a well thought-out integration roadmap. Here’s how to get started.

Daelight attended the recent BoxWorks conference to learn more about what Box is doing within the Life Sciences industry.

No 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.

Pharmacovigilance (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.