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September 25, 2019
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.
June 19, 2019
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.
March 19, 2019
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.
January 14, 2019
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.
November 28, 2018
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.
October 2, 2018
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.
September 11, 2018
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.
July 30, 2018
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.
June 13, 2018
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.