
💊 Pharma & Life Sciences
Clinical trials, lab samples, drug traceability and safety reporting. Open any template to see the finished diagram, then use it as the starting point for your own in the Studio.
11 templates
The states of a laboratory sample in a LIMS, from collection to reporting and disposal, with rejection and re-testing.
How a suspected side effect reported by a doctor or patient is captured, assessed and reported to the regulator on time (pharmacovigilance).
The systems that run a clinical trial: trial management, electronic data capture, randomisation, drug supply and safety reporting.
How medicine packs are serialised and traced from factory to pharmacy to stop counterfeits: unique codes, aggregation and verification.
How a pharmaceutical company prepares and files a marketing application (dossier) with regulators and handles their queries.
A schema for electronic batch records in pharmaceutical manufacturing: products, master recipes, batches, steps, materials used and deviations.
How a pharmaceutical plant handles a manufacturing deviation: report, impact assessment, root cause, CAPA and batch disposition.
How a site enrols a patient into a clinical trial: eligibility, consent, randomisation through the IRT and drug kit assignment.
An IoT deployment that watches vaccine temperatures from warehouse to clinic, with alerts when the cold chain breaks.
The long road from discovery to market for a new drug: research, preclinical, three clinical phases, approval and launch.
A drug safety platform that collects adverse event reports, codes them, detects signals and submits reports to regulators.
More Pharma & Life Sciences templates are being added regularly.