PHUSE Wiki

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Revision as of 06:38, 11 July 2019 by WendyDobson (talk | contribs)
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Welcome to the PhUSE Wiki


The PhUSE Wiki is an PhUSE/FDA/Industry collaboration to provide a medium to share information specifically relating to clinical trial informatics.


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Currently 6,835 users are helping to Connect, Share, Advance clinical informatics.


All content on this wiki is non-binding. All content expresses opinions of users and not necessarily that of their employer nor PhUSE. See our Disclaimers page

Need help with the Wiki? Ideas to Improve?

The Wiki Team are always looking at ways to improve this site. We want to make this user friendly, current and of benefit to PhUSE Members. If you have a question, query or need help, please use this 'Discussion Forum'. A member of the team will do their best to assist and all feedback is welcome. Equally should you wish to be part of the team, contact wendy@phuse.eu



PhUSE Events


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July Events: 18th Hoboken, New Jersey - 27th Bengaluru, India

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Registration is open, Early Bird closes 26th July

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Registration & Call for Papers open


Become a PhUSE Member

There are many benefits to becoming a PhUSE member. Here's just a few reasons why you want to become part of something amazing

  • Free attendance to a range of Single Day Events held across US, EU and Asia
  • Access to PhUSE News
  • Full access to PhUSE Archives
  • Participation in our annual US & EU Connects and the US Computational Science Symposium


To become a member, sign up here


Create a new Wiki page

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Working Group News


ANNOUNCEMENTS
PhUSE Webinars - Upcoming events and past presentations & recordings

Are you a PhUSE member? Log in to your account and visit the members blog to find a summary of CSS and all the latest news within the industry.

DELIVERABLES

We currently have deliverables out on public review. We encourage you to provide your feedback to the project leads by following the links below:

Implement Traceability in CDISC Compliant Studies

NEW PROJECTS

Projects that would be grateful to receive additional support and input are calling for volunteers. If you are able to dedicate a minimum of one hour per week, please contact workinggroups@phuse.eu to sign up.

This project will look to develop a white paper/presentation focussed on establishing the range of areas that need to be considered/impact on the use of real-world evidence in support of regulated clinical trial submissions.

  • SDSP-XML: A follow-on from the DRG-XML, this project will develop a machine-readable version of the Study Data Standardisation Plan as XML.





Industry News

GDPR has gone live. Please review PhUSE Privacy Policy

PhUSE Collaborations:

CDISC
FDA
HL7
PSI
STARDOG


Here's the link to the latest version of the Technical Conformance Guide (TCG) which has been updated by the FDA January 2019




Last revision by WendyDobson, 07/11/2019