Everything you need to know about Medical Affairs, in one place
Evidence-based articles with verified references on medical writing, medical affairs, medical education, healthcare AI, and regulatory compliance.
Medical Affairs / Industry
Regulatory and pharmaceutical market access trends.
How to build a medical dossier that withstands regulatory objections
A well-built dossier isn't written from the message — it's written from the evidence. GRADE classification, traceability, and compliance as lines of defense.
Read article → Medical Affairs / IndustryThe role of Medical Affairs in the pharmaceutical product lifecycle
From a function that documents what others decide, to a function that informs what the organization decides: the strategic evolution of Medical Affairs.
Read article → Medical Affairs / IndustryGPP 2022: what changes for sponsored scientific publication plans
The 2022 update expands GPP beyond clinical trials to any type of industry-sponsored biomedical research, with a practical checklist for publication planning.
Read article → Medical Affairs / IndustryWhat an MLR committee actually reviews before approving your medical material
Understanding what a Medical, Legal, and Regulatory review actually evaluates saves entire cycles of back-and-forth before material reaches the field.
Read article →Health Professions Education
Resources for the continuing education of clinical professionals.
Gamification in medical education: fad or evidence-based method?
It doesn't work just by including playful elements — it works when each game mechanic solves a specific learning problem. What the evidence says.
Read article → Health Professions EducationHow to design medical training that's actually remembered
Retention improves when the learner builds the knowledge, not when they receive it passively. Design principles backed by controlled trials.
Read article → Health Professions EducationProblem-based learning: what the evidence says in health professions training
PBL improves clinical skills and critical thinking, but the evidence level is still moderate — what that means for your training design.
Read article → Health Professions EducationSimulation and virtual reality in medical education: what actually improves
Less immersive VR outperformed fully immersive VR on knowledge outcomes. Pedagogical design matters more than hardware sophistication.
Read article →AI in Healthcare
Real use cases, with limits and evidence, not just promises.
Risks and biases of AI in scientific content generation
In marketing, a hallucination is a correctable error; in medical content, it's a patient safety risk. How to mitigate it with process, not just technology.
Read article → AI in HealthcareAI opportunity assessment: where your medical or commercial team should start
Budget isn't the main barrier to scaling AI. Start by mapping real bottlenecks, not by picking a tool.
Read article → AI in HealthcareHow reliable are AI-generated citations? What the evidence says
Only a third of AI-generated citations in one study were fully accurate on every metadata field. Why human verification remains non-negotiable.
Read article → AI in HealthcareFDA-EMA good AI practice principles: what they mean for your medical team
The first joint FDA-EMA document on AI in drug development sets ten principles — a useful common language even before formal guidance arrives.
Read article →Evidence & Compliance
Best practices in citation, traceability, and editorial quality.
How to avoid improper claims in pharmaceutical communication
The line between legitimate scientific information and improper advertising is precisely documented in Colombian regulation. How not to cross it by accident.
Read article → Evidence & ComplianceICMJE standards: what your team should know before publishing
A manuscript rejected for form is avoidable lost research time. Authorship criteria and the new ICMJE rules on AI.
Read article → Evidence & ComplianceBuilding a traceable scientific evidence matrix
A well-built evidence matrix supports every message with its exact source and exposes evidence gaps before a regulator finds them.
Read article → Evidence & ComplianceEQUATOR guidelines: how to choose the right reporting guideline before you write
Choosing the wrong reporting guideline late in the process means restructuring the whole manuscript. Here's how to get it right from the start.
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