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EDMS/RIMS Webinars

Electronic Document Management System (EDMS)

This webinar will provide participants with an overall understanding of EDMS from a business and technical point of view. The course will provide an introduction to EMDS application uses across a pharma company and include real life examples from across the industry in order to ensure that the content of the webinar is relevant and to allow participants to engage in dialogue with the instructors. New regulations and technology trends will also be included in the webinar and by the end of the course, the participants be able to engage in proficient collaboration with EMDS business partners. 

The main target audience of this webinar is employees working with EDMS or with tasks related to EDMS; e.g.  Regulatory affairs managers, TMF managers, technical support staff and IT project members.

 

The course is carried out as a webinar and has a duration of 2 hours.

 

Regulatory Information Management System (RIMS)

This webinar will provide participants with an overall understanding of RIMS from a business and technology point of view. This webinar will discuss RIMS using real life examples from across the industry, which will ensure that the content is relevant and allow for participants to engage in dialogue with the instructors. New regulations and technology trends will also be included in this webinar and by the end of the course, the participants should be able to engage in proficient collaboration with RIMS business partners.

The main target audience of this webinar is employees working with RIMS or with tasks related to RIMS; e.g. submission compilation managers, technical support staff and IT project members.

 

The course is carried out as a webinar and has a duration of 2 hours.

 


Registration
If you are interested in attending any of these webinars, you can request to be contacted by one of our instructors in order to schedule your participation and adjust to any special requirements that you might have. Please fill out your contact details below and choose either "EDMS Webinar" or "RIMS Webinar" in the course dropdown menu. We will then get in touch with you as soon as possible. The price for participating in any of the two courses is DKK 1000 per participant. The price will be subject to change depending on the requirements of your organization.​

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Niels Buch Leander +45 3075 5339nbln@nnit.comManaging Consultanthttps://www.linkedin.com/in/nielsbuchleanderNiels Buch Leander

 

 

Understanding Clinical Development and Systemshttps://www.nnit.com/OfferingsAndArticles/Pages/Understanding-Clinical-Development.aspxUnderstanding Clinical Development and Systems
Trial Master File and Document Managementhttps://www.nnit.com/OfferingsAndArticles/Pages/TMF.aspxTrial Master File and Document Management
Regulatory Processes and Systemshttps://www.nnit.com/OfferingsAndArticles/Pages/Regulatory-Processes-and-Systems.aspxRegulatory Processes and Systems
Regulatory Affairshttps://www.nnit.com/OfferingsAndArticles/Pages/Regulatory-Affairs.aspxRegulatory Affairs
Pharmacovigilance, PV and Drug Safetyhttps://www.nnit.com/OfferingsAndArticles/Pages/Pharmacovigilance,-PV-and-Drug-safety.aspxPharmacovigilance, PV and Drug Safety
EMA SPOR/IDMP and MDMhttps://www.nnit.com/OfferingsAndArticles/Pages/EMA-SPOR-and-MDM-.aspxEMA SPOR/IDMP and MDM
Pharma Basicshttps://www.nnit.com/OfferingsAndArticles/Pages/Pharma-Basics.aspxPharma Basics