Lab report · 20 Sep
LESS ADMIN. MORE TIME FOR CARE.
Less typing.
More time for your patients.
Bring records, reports and longitudinal signals into one source-linked view. Explore private voice dictation designed to reduce typing and make documentation review easier—with the clinician checking accuracy before anything is used.
Private dictation pilot: English, synthetic training data only. Transcribe → edit → review. Real-patient use, accuracy and time savings require validation. No diagnosis or prescribing.
Synthetic patient
Source-linked
PATIENT CONTEXT
Samira K.
Synthetic preview · illustrative sources
Review required
Status preserved
Every fact keeps its source.
Original evidence, version and review decision stay together.
PHARMACY EXPERIENCE. TRACEABLE MEDICATION EVIDENCE.
35 years of pharmacy experience.
A clear path back to the source.
Founded by Alfan Mithani, RPh, MFIT, a Canadian pharmacist with 35 years of practice experience. Simply Clinical is being developed around the medication-information questions clinicians need to investigate and review.
Drug information with context.
Explore U.S. drug-label and Canadian drug-record libraries in the pilot. Record types, countries and coverage limits remain visible; a product record is not a clinical recommendation.
Evidence you can inspect.
The synthetic evidence-navigation workflow presents source passages with document dates and links so reviewers can check the original material.
Professional judgment stays central.
AI helps navigate evidence. The clinician verifies relevance, formulation, country and document version before considering any clinical use.
Current status: synthetic-only evidence-navigation pilot. Clinical accuracy, time savings and comparative performance have not yet been established. Founder experience is not a substitute for product validation.
GET SIMPL AI HEALTHCARE SUITE
Three products. One permissioned history.
Simply Wearable organizes device observations. Simply Med History retains the longitudinal record. Simply Clinical prepares source-linked context for human review.
Explore the synthetic diabetes workflow. Production cross-product access requires verified patient mappings and explicit grants; the public demo does not connect real accounts.
No clinical validation or regulatory approval is claimed. Do not send patient information through the contact form.
ONE CLINICAL VIEW
Less hunting.
More useful context.
Designed around the moment a clinician needs to understand what changed, where it came from and what still needs review.
Bring context together.
Records, reports and longitudinal signals appear in one permissioned view.
Inspect the evidence.
Every imported fact retains its source, timestamp, version and provenance.
Make the decision.
The clinician accepts, corrects or rejects. Nothing acts autonomously.
BUILT-IN SAFETY
Assist judgement.
Never replace it.
Human review at every step
Imported information remains outside the clinical context until reviewed.
Provenance that stays attached
Source evidence and clinical decisions are recorded together.
Deliberately bounded assistance
No autonomous diagnosis, prescription, order or clinical execution.
PROPOSED UAE CLINICAL PILOT
Start safely. Prove value.
Decide together.
A six-week, synthetic-first sandbox pilot for a small clinical team—with agreed measures, explicit safety gates and no production data.
Explore a pilot