Main Page: Difference between revisions
No edit summary |
(New Page) |
||
| Line 1: | Line 1: | ||
'''Welcome!''' | |||
''' | |||
This site supports the installation, deployment and full documentation of OpenRIMS modules for Registration and Permits & the PV module OpenPV. | |||
'' | '''Navigation & Language''' | ||
Please click All Pages link on the left to see an index of all content of this Wiki. | |||
To change language please use Chrome and then Right Click to select Translate to select a language. The system uses Google Translate which might not always be 100% accurate. | |||
'''Content''' | |||
Click the links below or use the search box on the top right. | |||
'''What is a RIMS?''' | |||
The purpose of a Regulatory Information Management System (RIMS) is to automate and digitalize the processes and work routines at a National Medicines Regulatory Authority (NMRA). | |||
OpenRIMS serves that purpose and is built on [[Common Standards for RIMS]]. | |||
'''Getting Started''' | |||
* [[OpenRIMS - Installation Part 1|OpenRIMS Installation/Deployment Part 1]] | |||
* User Guide for Pharmaceutical Manufacturers, Pharmacy Owners and other Clients of Regulatory Authorities | * [[OpenRIMS - Installation Part 2|OpenRIMS Installation/Deployment Part 2]] | ||
* OpenRIMS Localization | |||
* [[OpenRIMS - User Management|OpenRIMS User Management]] | |||
* [[OpenRIMS - Workflows Part 1|OpenRIMS Workflow Configuration]] | |||
* [[OpenRIMS - Reporting Google Part 1|OpenRIMS and Google Looker Studio]] | |||
'''The Common Regulatory Function''' | |||
* [[OpenRIMS - Marketing Authorization Part 1|OpenRIMS M2 - Marketing Authorization]] | |||
* [[OpenPV - Overview Part 1|OpenPV M3 - Pharmacovigilance]] | |||
* OpenRIMS M4 - Import/Export Certificates - Coming Soon! | |||
* OpenRIMS M5 - Premises and People Registration - Coming Soon! | |||
* OpenRIMS M6 - Inspection - Coming Soon! | |||
* OpenRIMS M8 - Clinical Trial Approval - Coming Soon! | |||
'''Making content contributions''' | |||
'''PLEASE NOTE!''' | |||
Use the following syntax to name the pages: | |||
''"System name"_"Page/Subject Title"_"Part Number"'' | |||
Example: | |||
'''OpenRIMS_Cleaning the Database_Part 1''' | |||
All new content is subject to review and approval. | |||
OpenRIMS reserves the right to edit or delete content or pages as appropriate if the content is not relevant for Regulatory Information Management Systems. | |||
'''User Guides for each Module''' | |||
* User Guide for Pharmaceutical Manufacturers, Pharmacy Owners and other Clients of Regulatory Authorities | |||
* User Guide for Regulatory Staff | * User Guide for Regulatory Staff | ||
* User Guide for System Administrators | * User Guide for System Administrators | ||
Revision as of 18:17, 20 July 2023
Welcome!
This site supports the installation, deployment and full documentation of OpenRIMS modules for Registration and Permits & the PV module OpenPV.
Navigation & Language
Please click All Pages link on the left to see an index of all content of this Wiki.
To change language please use Chrome and then Right Click to select Translate to select a language. The system uses Google Translate which might not always be 100% accurate.
Content
Click the links below or use the search box on the top right.
What is a RIMS?
The purpose of a Regulatory Information Management System (RIMS) is to automate and digitalize the processes and work routines at a National Medicines Regulatory Authority (NMRA).
OpenRIMS serves that purpose and is built on Common Standards for RIMS.
Getting Started
- OpenRIMS Installation/Deployment Part 1
- OpenRIMS Installation/Deployment Part 2
- OpenRIMS Localization
- OpenRIMS User Management
- OpenRIMS Workflow Configuration
- OpenRIMS and Google Looker Studio
The Common Regulatory Function
- OpenRIMS M2 - Marketing Authorization
- OpenPV M3 - Pharmacovigilance
- OpenRIMS M4 - Import/Export Certificates - Coming Soon!
- OpenRIMS M5 - Premises and People Registration - Coming Soon!
- OpenRIMS M6 - Inspection - Coming Soon!
- OpenRIMS M8 - Clinical Trial Approval - Coming Soon!
Making content contributions
PLEASE NOTE!
Use the following syntax to name the pages:
"System name"_"Page/Subject Title"_"Part Number"
Example:
OpenRIMS_Cleaning the Database_Part 1
All new content is subject to review and approval.
OpenRIMS reserves the right to edit or delete content or pages as appropriate if the content is not relevant for Regulatory Information Management Systems.
User Guides for each Module
- User Guide for Pharmaceutical Manufacturers, Pharmacy Owners and other Clients of Regulatory Authorities
- User Guide for Regulatory Staff
- User Guide for System Administrators