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Veeva R&D Summit: Our Top Takeaways

Veeva R&D Summit: Our Top Takeaways

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

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InSight and Power Business Intelligence: Improving Data Aggregation and Reporting in Life Sciences

InSight and Power Business Intelligence: Improving Data Aggregation and Reporting in Life Sciences

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

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Hot Topics at DIA RSIDM 2019: IDMP

Hot Topics at DIA RSIDM 2019: IDMP

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.

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Data-Driven Machine Learning Solution With Box Skills

Data-Driven Machine Learning Solution With Box Skills

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

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Developing an M&A Playbook for Your IT Organization

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.

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Strategic Systems Integration: Considerations for a Post-Merger Roadmap

Strategic Systems Integration: Considerations for a Post-Merger Roadmap

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

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BoxWorks Recap: Managing Regulated Content Within the Life Sciences Industry

BoxWorks Recap: Managing Regulated Content Within the Life Sciences Industry

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

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Daelight Solutions

Why IT Needs a Seat at the Table During Due Diligence

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.

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Are You Thinking About Pharmacovigilance Inspection Readiness?

Are You Thinking About Pharmacovigilance Inspection Readiness?

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.

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