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[[File:Logo OpenRIMS.png|thumb]]
'''Welcome!'''
'''Please Note!'''


''We are currently uploading all system documentation to this platform.''
This site supports the installation, deployment and full documentation of OpenRIMS modules for Registration and Permits & the PV module OpenPV.


''The process is estimated to conclude by August 2022.''
'''Navigation & Language'''


''This will go hand in hand with rebranding to OpenRIMS which logo is seen to the right.''
Please click All Pages link on the left to see an index of all content of this Wiki.


Choose Module:
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.


* OpenRIMS M2 - Marketing Authorization
'''Content'''
* OpenRIMS M3 - Pharmacovigilance
* OpenRIMS M4 - Import/Export
* OpenRIMS M5 - Pharmacy Registration
* OpenRIMS M6 - Pharmacy Inspection
* OpenRIMS M8 - Clinical Trial


Or choose Function:
Click the links below or use the search box on the top right.


*[[Installation Part 1|Installation/Deployment Part 1]]
'''What is a RIMS?'''
*[[Installation Part 2|Installation/Deployment Part 2]]
*[[User Management]]
*[[Workflows Part 1|Workflow Configuration]]


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).


Technical Links for this Wiki:
OpenRIMS serves that purpose and is built on [[Common Standards for RIMS]].


# [[Allpages|All Pages Index]]
'''Getting Started'''


== Main Links for each Module ==
* [[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

The Common Regulatory Function

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