Abstract: A system generates executable prior authorization drug request rules using a compiler. A data repository stores drug criteria. The system is configured to generate a criteria specification user interface that enables a user to specify exclusion criteria, inclusion criteria, preferred or step therapy criteria, concurrent therapy criteria, assessment criteria, quantity limits, and/or refill instructions. A prescription prior authorization rules compiler module is configured to access a criteria specification for the drug from the repository and to automatically compile the criteria specification into executable prescription prior authorization rules. A drug criteria object generation module is configured to generate a drug criteria object for the drug, including drug criteria object identification information, the executable prescription prior authorization rules, a data dictionary, and/or canonical data.

Abstract: Roughly described, a user instantiates protocol elements in a structured clinical trial protocol database and then draws from them in the development of one or more protocol related documents. The system helps the user select tasks to be performed during the study by reference to a historical database of tasks previously associated with similar protocols. The system automatically generates complex content from protocol elements in the database, and can render overlapping sets of protocol elements differently at different locations in the document. The system can automatically provide advisories indicating aspects of the document that still require completion or highlighting other issues that a sponsoring authority deems important for the document type. After all protocol elements are instantiated in the protocol database, it can then be used to drive the operation of most downstream aspects of the study.

Abstract: Roughly described, a user instantiates protocol elements in a structured clinical trial protocol database and then draws from them in the development of one or more protocol related documents. The system helps the user select tasks to be performed during the study by reference to a historical database of tasks previously associated with similar protocols. The system automatically generates complex content from protocol elements in the database, and can render overlapping sets of protocol elements differently at different locations in the document. The system can automatically provide advisories indicating aspects of the document that still require completion or highlighting other issues that a sponsoring authority deems important for the document type. After all protocol elements are instantiated in the protocol database, it can then be used to drive the operation of most downstream aspects of the study.