Drug document production system

• US 6,205,455 B1
• Filed: 07/13/1999
• Issued: 03/20/2001
• Est. Priority Date: 04/27/1995
• Status: Expired due to Term

• Current Assignee: Michael UMEN & Company Incorporated
• Original Assignee: Michael UMEN & Company Incorporated
• Inventors: Wilson, Phillip C., Martin, Erik A., Umen, Michael J., Nomides, Kathy J.
• Primary Examiner(s): CHOULES, JACK M
• Application Number:
  US09/351,848
• Time in Patent Office: 616 Days
• Field of Search: 707/1, 707/3, 707/104, 707/511, 707/531, 707/513
• US Class Current: 715/236
• CPC Class Codes: G06F 40/166 Editing, e.g. inserting or deleting
• CPC Class Codes: G06Q 10/10 Office automation; Time management
• CPC Class Codes: G06Q 30/02 Marketing; Price estimation or determination; Fundraising
• CPC Class Codes: G16H 10/20 for electronic clinical trials or questionnaires
• CPC Class Codes: G16H 15/00 ICT specially adapted for medical reports, e.g. generation or transmission thereof
• CPC Class Codes: G16H 40/63 for local operation
• CPC Class Codes: G16H 70/40 relating to drugs, e.g. their side effects or intended usage
• CPC Class Codes: Y10S 707/99931 Database or file accessing
• CPC Class Codes: Y10S 707/99933 Query processing, i.e. searching

Abstract

A document production system is provided for preparing documents and managing a database of information pertaining to investigational studies of medical products. The document production system includes a data management user interface for providing user access to the database and for retrieving information from the database as specified by selected document templates for placement into word processor-compatible documents. Additionally, the data management user interface is capable of updating information stored within the database in accordance with information specified within a previously-prepared document.

Claims

1. An apparatus for producing a document for regulatory review of a drug, comprising:

a first electronic document template corresponding to a first regulatory authority for approving use of the drug within a first jurisdiction;

a second electronic document template corresponding to a second regulatory authority for approving use of the drug within a second jurisdiction;

a data storage system for storing said first and second templates and for storing a database for containing information pertaining to investigational studies of the drug;

a computer connection with the data storage system, the computer configured to execute a data management interface integrated with a word processor, for storing and retrieving information in the database, and for composing said information to form the document on the basis of a selected one of said first and second templates; and

wherein said data management interface is configured to generating a status report indicating a status of completion of said information stored in the database.

4. The apparatus of claim 1 wherein said database is configured to store alternative versions of a data item pertaining to the drug, and wherein the data management interface is arranged to select a corresponding one of said versions for inclusion in the document on the basis of the selected template.

2. An apparatus for producing a document for regulatory review of a drug, comprising:

a first electronic document template corresponding to a first regulatory authority for approving use of the drug within a first jurisdiction;

a second electronic document template corresponding to a second regulatory authority for approving use of the drug within a second jurisdiction;

a data storage system for storing said first and second templates and for storing a database for containing information pertaining to investigational studies of the drug;

a computer connection with the data storage system, the computer configured to execute a data management interface integrated with a word processor, for storing and retrieving information in the database, and for composing said information to form the document on the basis of a selected one of said first and second templates; and

wherein said database is configured to store alternative versions of a data item pertaining to the drug, and wherein the data management interface is arranged to select a corresponding one of said versions for inclusion in the document on the basis of the selected template.

3. The apparatus of claim 2 wherein the document is made available for manipulation within the word processor after composition, and wherein the data management interface is configured to update the information stored in the database on the basis of changes made to the document with the word processor.