Medical Publications Are Evolving. Is Your Organization?
The greatest risk to your scientific narrative isn’t poor science—it’s inconsistency
Every year, medical communications teams invest significant resources generating high-quality evidence through publications, congress presentations, advisory boards, and clinical research. Yet as that evidence is translated into HCP materials, field…
How efficient is your content review process?
For pharmaceutical, biotech, and medical device organizations, every review delay can impact campaign timelines, product communications, and stakeholder engagement. The challenge isn’t just reviewing content. It’s doing so efficiently while…
End-to-End Regulatory Writing Support: From Protocol to Submission
Many sponsors think of regulatory writing as a series of individual deliverables. A protocol. An Investigator’s Brochure. A clinical study report. A briefing document. But health authorities don’t review these…
Aligning Science, Stakeholders, and Strategy
Today’s scientific ecosystem is more interconnected than ever. Clinical development teams, Medical Affairs, investigators, regulators, advocacy organizations, publication professionals, and other stakeholders all contribute to advancing medical evidence. Yet even…
Publication planning is more than a timeline—it’s a living strategy
A publication plan isn’t something you create once and put on a shelf. As clinical milestones shift, data mature, stakeholder priorities evolve, and regional needs emerge, publication strategies must continuously…
Turn complex data into clear, compelling visual stories
Great science deserves to be understood. In today’s fast-paced medical communications environment, effective data visualization is essential for transforming complex findings into insights that resonate with diverse audiences. The right…
Happy 4th of July from Med Communications!
We wish our American colleagues, clients, and partners a safe, fun, and memorable Independence Day spent with family and friends. While many are celebrating, Med Communications remains committed to providing…
Publications Are No Longer Enough. Integrated Evidence Planning Is the Future.
As healthcare stakeholders demand more comprehensive evidence to inform decisions, publication planning can no longer operate in isolation. Today’s value story is built from multiple evidence streams:🟦 Clinical trial data🟦…
Standardizing Clinical Protocols for Global Success: ICH M11 (CeSHarP)
Clinical protocols are being redefined, and ICH M11 is leading the shift. The introduction of ICH M11 and the Clinical Electronic Structured Harmonised Protocol (CeSHarP) template provides a global standard…