Whether you are a company scientist, license partner, academic researcher, or CROs, today’s drug discovery research and development operation for biopharmaceutical companies require creating, managing, and executing thousands of in-vitro and in-vivo screening assays through traditional or high throughput systems involving chemistry, genomics, biomarkers, animals and human subjects.
Without a comprehensive digital protocol registration system, organizations are prone to mistakes due to massive data entry requirements.
With Labwise XD – Global Research Protocol Registration, you can:
Labwise XD manages all protocol registry functions, including ADME, functional genomics, preclinical studies, high throughput screens (HTS), SAR, internal and external panel screenings, and chemical processes, including the recording of single or multi-step reactions.
Includes tasks, favorites, charts, and lists based on role.
Searches include metadata and draw chemistry structures/reactions; searches documents globally using simple and faceted searches.
Includes unique numbering schemes for auto-generated IDs and granular security for scientist teams.
Allows collection of experimental data used in protocol – from the media to the experimental conditions.
Allows for the creation and collection of groups, subjects, treatments, and dosing metadata with the relation between them.
Utilizes one common workflow for the collection of data across different screen types, providing only relevant fields within the workflows.
Integrates with active directory and customer RIF systems for master code set values, project data, target data, metadata, and critical flags.
Triggers with permission-based actions, approval tasks, versioning of metadata and report, and locking of editings.
Automatically creates protocol documents based on metadata with onscreen preview and in Word.
Migrates legacy data/records and creates new protocol records from imports.
Reduces time to initialize a new protocol with similar values.
Allows changes over multiple records.