Insights and practical guides
Clinical research, oncology and medical technology—made clear
Source-linked analysis for patients, research teams, sponsors, health-tech companies and professional audiences.
How to find a clinical trial: a safe, step-by-step search
How to use ClinicalTrials.gov, review locations and eligibility criteria, verify Russian records and contact a research site.
Clinical research · ExplainerInterventional and observational studies: what a registry record means
A plain-language guide to study types, phases, statuses, interventions, eligibility and locations in ClinicalTrials.gov.
MIKA.help · Patient navigationHow MIKA approaches clinical-trial navigation
A transparent account of registry discovery, criteria review, Russian verification and direct site confirmation in the MIKA workflow.
Oncology · Clinical researchClinical trials in oncology: why they matter and what participation involves
What oncology trials investigate, how screening and informed consent work, and why participation is always voluntary.
Sponsors & CROs · Site operationsHow a modern oncology clinical-research team works
A practical framework for evidence-based feasibility, role allocation, recruitment, training, quality by design and sponsor communication.
Medical AI · Responsible adoptionArtificial intelligence in medicine: useful support, real limits
Where AI can support medicine and research, why human oversight and data governance matter, and which claims should be avoided.
Health-tech · Product developmentFrom a medical idea to a usable product
A product-development route from clinical problem and intended use to evidence, pilot implementation and responsible scale-up.
Geriatrics · Healthy longevityHealthy longevity: function, resilience and person-centred care
Why healthy ageing focuses on functional ability, comprehensive assessment and meaningful goals rather than a single longevity metric.
GxP · Quality standardsGCP, GLP and GMP: three standards, three different questions
A practical comparison of Good Clinical Practice, Good Laboratory Practice and Good Manufacturing Practice across the medical-product lifecycle.
Preclinical development · GLPPreclinical drug development: preparing a scientific hypothesis for clinical research
Pharmacology, ADME and pharmacokinetics, toxicology, GLP, CMC and the evidence needed before first studies involving people.
Patients · Safe data sharingHow to prepare medical records for a digital service
A practical guide to selecting relevant medical records, preparing an oncology record set and reducing direct identifiers before digital sharing.