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The eClinical Forum is a global network of peers. It provides a non‐competitive environment for innovation, learning and collaboration in clinical research.

 

NEWS FROM THE ECF

BoF Discussion: Archiving – who is responsible and how should we support them?

Wed Feb 21 2018 for one hour

BoF Discussion: Archiving – who is responsible and how should we support them?

This webinar looks to set up a discussion of possible archiving alternatives and how practical they are.  Facilitated by Alan Yeomans, Pharmaceutical Consulting Group.  Participants are encouraged to share their ideas and experiences!!

This webinar is for eCF Members only. Please contact suzanne.bishop@eclinicalforum.org for additional information on registration to this event or membership.

Webinar: Social Media in Clinical Trials: Going beyond Patient Recruitment

Feb 7 2018 at UTC 1500 for one hour

Webinar: Social Media in Clinical Trials: Going beyond Patient Recruitment

Presented by Les Jordan, Target Health

When most people think of social media in clinical trials, what comes to mind is using social media platforms for patient recruitment.  And while recruiting subjects through social media is a great use case, those platforms can be used for far more.  In this webinar we’ll discuss using social media across the clinical trial value chain along with a quick review of the various platforms in the marketplace.  Our discussion will include:

- Patient Recruitment 
- Patient Retention
- Building lasting patient communities 
- Safety monitoring

Webinar is for eClinical Forum members only. Please contact Suzanne.Bishop@eclinicalforum.org for registration.

BoF Webinar: ICHOM (International Consortium for Health Outcomes Measurement) GLOBE project

Tuesday 25-July-2017 -- Registration Required

BoF Webinar: ICHOM (International Consortium for Health Outcomes Measurement) GLOBE project

Facilitator: Barbara Skerrit, ICON        

 

Time: UTC 1300;  (eg 15:00 CEST, 9:00 AM EDT, 9:00 PM Singapore).  We apologize for the inconvenient timeslot in some regions.    

Duration: one hour     

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eCF Autumn North America Meeting Oct 16-18 2017

Babson College, Wellesely MA hosted by eClinical Solutions

  • 10/15/2017 - 10/18/2017
  • Author: NA Administrator
  • Number of views: 6877
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eCF Autumn North America Meeting Oct 16-18 2017

We are happy to announce that our Autumn meeting will be held at the Babson Executive Conference Center in Wellesley MA on Oct 16-18 2017. Thank you to eClinical Solutions for hosting us in such a nice location.  It is 35 mins from Logan Airport and 25 mins from the Amtrak station in Boston Back Bay. This is a full-featured executive conference facility which includes guest rooms and dining areas.

A Preliminary Agenda will be sent in July. Please send suggestions for topics/presenters to info@eclinicalforum.org.

 

Technology Showcase Webinar: "Developing Your eConsent Strategy - Best Practices "

5 July 2017: Registration Required

Technology Showcase Webinar: "Developing Your eConsent Strategy - Best Practices "

Presented by:  Michael Tucker, Senior Product Solutions Specialist, Medidata Solutions

 

Open To: Staff from eClinical Forum member companies

Date : Wed, 5-July-2017         Duration: One hour

Time: UTC 1300:   (09:00 AM EDT, 15:00 CEST, 9:00 PM Singapore)  We apologize for the inconvenient time in some regions.

Click on title for more information

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BoF Round-table Discussion: Considerations and challenges for electronic research data archival at sites using direct download

BoF Round-table Discussion: Considerations and challenges for electronic research data archival at sites using direct download

The implementation of new solutions to share electronically the eCRF PDFs with sites have brought up new considerations and challenges to this process.

We would like everyone to share their experiences on how the process has been implemented, as well as the challenges experienced. This will be a group discussion on the recommendations to make this process as straight forward as possible for Sites and Sponsors, while complying with requirements.

Facilitated by Carmen Jiménez, Eli Lilly

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Position Paper: Trial Master File Archiving and the Decommissioning of Computerised Systems Used in Clinical Trials, PR1

Position Paper: Trial Master File Archiving and the Decommissioning of Computerised Systems Used in Clinical Trials, PR1

The eClinical Forum is happy to announce the public release of a position paper titled “Decentralized TMF Archives and The Decommissioning Of Computerised Systems Used In Clinical Trials”.  This position paper was written by a joint task force from EUCROF and the eClinical Forum, with representatives from other industry associations including ECRIN, the ePRO consortium, Medicines for Europe and the RQA.

ABOUT THE POSITION PAPER: Following the completion of a clinical trial, the essential documents that make up the TMF (Trial Master File) are retained and archived by the sponsor, the investigator and, in some cases, sub-contractors to the sponsor and/or investigator. The position paper highlights 11 key positions: seven positions concerning the archiving of the TMF and four positions concerning the archiving of the electronic data. These positions address areas where regulatory expectations are not always seen as being aligned with industry practices.

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Birds-of-a-Feather Webinar: Practical Considerations when implementing eConsent

Birds-of-a-Feather Webinar: Practical Considerations when implementing eConsent

This webinar introduces the NEW "Practical Guide to eConsent" which addresses key themes and hots topics and provides a view on the modernization of the clinical trials informed consenting process, including the current perception shift of eConsent adoption in light of the COVID-19 pandemic.  This is a joint work by the eClinical Forum and EUCROF.

 

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Birds-of-a-Feather Round Table Discussion:  “When does audit trail begin?”

Birds-of-a-Feather Round Table Discussion: “When does audit trail begin?”

Audit trails create a step-by-step record of data back to its source. It is utilized when the integrity and confidence of the datapoint has critical/legal significance. It is important to determine and declare when data entry becomes “real” data. In legacy paper, data is manually recorded, but only becomes “real” when it is signed, submitted, or completed. Signatures and confirmations also exist to add additional credibility to the source. If a paper form is being filled, it is considered draft until it is declared complete by the originator. The originator has the option to crumple up the “draft” paper and start another without question. The same should hold true with electronic data entry as this webinar will discuss.

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