Solutions
Organised by who you are.
MedClariva, described by the problem it solves rather than the modules it contains.
For pharmaceutical companies and CROs
Run a safety system that survives an inspection.
For marketing authorisation holders without a full in-house safety function, and for service providers who need to demonstrate control rather than describe it.
- ICSR intake, medical review and quality control
- Signal detection with disproportionality analysis and structured assessment
- Aggregate reporting — PBRER, PSUR, DSUR, PADER
- Risk management plan authoring and benefit-risk synthesis
- Literature surveillance and causality assessment
- Regulatory intelligence across EMA, MHRA, FDA and CDSCO/PvPI
- PSMF maintenance and QPPV oversight
- CAPA, vendor oversight and inspection readiness
- Competency training and assessment for safety staff
For healthcare professionals
Training that assesses judgement, not recall.
For clinicians and life-sciences graduates moving into pharmacovigilance and medical affairs, and for employers who need to know whether a hire can actually do the work.
- Case-based assessment against structured competency rubrics
- Role pathways — PV associate, drug safety physician, QPPV and oversight
- Scoring on causality, seriousness, expectedness and submission decisions
- A realistic case bank, not worked examples with the answer attached
- Free browser-based tools for extraction and E2B(R3) validation
Get in touch
Tell us what you are building.
Partnership, pilot, procurement or investment — enquiries are read and answered by the founder, not a queue.