Other names: maude_database
A Cross-sectional Analysis of the US Food and Drug Administration Manufacturer and User Facility Device Experience Database.
data management pharmacovigilance human
CFM is a database of experimentally validated protocols for chemical compound-based direct reprogramming and transdifferentiation.
The FDA Medical Devices ontology categorises FDA-approved medical devices. If you work on the project responsible for "FDA Medical Devices" then please consider helping us by claiming this record and ...
The Global Unique Device Identification Database (GUDID - pronounced "Good ID") is a database administered by the FDA as part of the UDI system. The GUDID contains device identification information su ...
BRIDG is a domain analysis model that represents the realm of protocol-driven clinical, pre-clinical, translational and basic research. This breadth includes concepts from Common (i.e., concepts share ...
A cross-sectional analysis of the emergency events database from a pediatric perspective. The international disasters database. Disaster group: Two main groups of disasters are distinguished in EM-D ...
Define-XML transmits metadata that describes any tabular dataset structure. When used with the CDISC content standards, it provides the metadata for human and animal model datasets using the SDTM and/ ...
Food and Agriculture Organization Corporate Statistical Database (FAOSTAT) provides free access to food and agriculture data for over 245 countries and territories and covers all FAO regional grouping ...
The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA.
The pharmacovigilance ontology connects known facts on drugs, disease, ADEs, and their molecular mechanisms.
A mesocosm database management system for environmental nanosafety.
LINCS Production Phase 2 Extended Metadata Standards were developed by the LINCS consortium with the goal of generating an integrated view across the diverse LINCS data resources. These guidelines are ...
Veterans Health Administration National Drug File is a centrally maintained electronic drug list used by the VHA hospitals and clinics. Facilities use the NDF to check drug interactions, to manage ord ...
NCI Thesaurus (NCIt) provides reference terminology for many NCI and other systems. It covers vocabulary for clinical care, translational and basic research and public information.
Based on the needs of national scientific and technological innovation for laboratory animal resources, we use various methods such as foreign introduction, domestic collection, independent research a ...
GLIS is made available according to Art. 17 of the International Treaty to facilitate access and exchange, based on existing information systems, on scientific, technical and environmental matters rel ...
The need to represent knowledge about food is central to many human activities including agriculture, medicine, food safety inspection, shopping patterns, and sustainable development. FoodOn is built ...
PharmGKB is a resource that provides information about how human genetic variation affects response to medications. PharmGKB collects, curates and disseminates knowledge about clinically actionable ge ...
DrugCentral is online drug information that provides information on active ingredients, chemical entities, pharmaceutical products, drug mode of action, indications, and pharmacologic mode of action. ...
>>>>!!<<<< As stated 2017-11-23 the database is not available anymore >>>>!!<<<< ACEpepDB is a database ran by the Central Food Technological Research Institute. It contains records of about 865 pepti ...
Mining drug-target and drug-adverse drug reaction databases to identify target-adverse drug reaction relationships.