DIAアカウントをお持ちの場合、サインインしてください。

サインイン

ユーザーIDをお忘れですか? or パスワードをお忘れですか?

Bethesda North Marriott Hotel and Conference Center

2017年2月06日 (月) 午前 7:00 - 2017年2月08日 (水) 午後 5:00

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

Regulatory Submissions, Information, and Document Management Forum

Session 2 Track 3: EDMS in the 21st Century, Better, Broader, More Flexible

Session Chair(s)

Dimitri  Stamatiadis, PHD, MBA

Dimitri Stamatiadis, PHD, MBA

CEO

Maia Consulting, Switzerland

EDMS has been around for a long time and appeared to have reached a quiet maturity. But technology has once more surprised us, and in more than one way. In the past few years EDMS moved to the cloud, became metadata driven and adopted a flexible cost model. At the same time, new content came onboard with the addition of eTMF triggering additional functionality. But if regulatory documents are organized with CTD dossier submission in mind, how can other documentation be transferred to HAs? Are we getting ready to submit eTMFs? Finally, EDMS technologies have become accessible to smaller companies thanks to a flexible cost model and the development of standards such as the DIA reference models. Now, small companies have Pocket EDMS, a free, simple, standardised protocol for choosing the right vendor also developed within the DIA framework. Definitely EDMS is alive and kicking.

Learning Objective : Attendees, especially from smaller pharma companies, consultants and vendors will get direct benefit from learning about this free-to-use packaged EDMS implementation protocol developed as a DIA initiative "by the industry, for the industry"

Speaker(s)

Dimitri  Stamatiadis, PHD, MBA

Pocket EDMS a DIA initiative for Small and Medium Pharma and Biotech

Dimitri Stamatiadis, PHD, MBA

Maia Consulting, Switzerland

CEO

Rick  London

The Future of DMS Design and User Experience

Rick London

GlobalSubmit, United States

Product Manager

Patricia  Santos-Serrao, RAC

Bringing TMF and eCTD Together: Is Your TMF Submission Ready?

Patricia Santos-Serrao, RAC

MasterControl, United States

Director of Product Management, Pharmaceuticals and Biologics

最新情報や機会を逃さないで

DIAのメールを購読すれば、常に最新の業界情報やイベント情報を得ることができます。