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Hi Sarah,

 

Please feel free to contact me off list for more details but I can probably
help you. I have worked with several organisations to procure and implement
eTMF solutions. The marketplace is still relatively immature but the number
of products is increasing all the time. Refreshingly, there are now some
good solutions that are more affordable to academia, investigator sites and
smaller biopharmaceutical companies, rather than the huge multi-national
sponsors. My  <http://rammell-consulting.co.uk/> website provides a little
information about these products but I'm happy to be contacted to discuss
further. You may also find some very useful hints and tips on two LinkedIn
groups: "Clinical Records Management" and "TMF Reference Model"

 

Regards,

Eldin.

 

Eldin Rammell

Managing Director,  <http://rammell-consulting.co.uk/> RAMMELL Consulting
Ltd

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From: The Information and Records Management Society mailing list
[mailto:[log in to unmask]] On Behalf Of Sarah Phillips
Sent: 07 March 2012 16:43
To: [log in to unmask]
Subject: Electronic Trial Master File

 

Dear All, 

Apologies for cross posting. 

We're currently investigating the feasibility of investing in some form of
EDRMS specifically for our clinical trial records only.  I understand that
there are some packages aimed at managing electronic trial master files out
there - I was just wondering if anyone on the list has any experience of
implementing such a product and if so which sort of product you'd gone for? 

Any information gratefully received, and I'm happy to send a summary of
responses back to the list. 

Best wishes, 

Sarah   

Sarah Phillips
University Records Manager
Governance & Compliance Division
Cardiff University
McKenzie House
30-36 Newport Road
Cardiff
CF24 0DE
029 20879403
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