Using CDISC standardized content to establish a clinical metadata repository This presentation from the CDISC Europe Interchange 2013 explains how a clinical MDR can be established using CDISC standardized content, in
It's just over 2 weeks till #PhUSE US Connect in Orlando!! 😀 Come and chat to us at booth 21 and tell us how we can help with your clinical trials! You'll even get the chance to win a bottle of fine Scotch! 👍
We’re working with our client who wants to implement a metadata repository to manage their internal standards. The goal is to import existing standards into the metadata repository and to set up governance and approval processes. Can we help you too?https://t.co/WNOe9Qlsma
Heading to #ACDM in Dublin anyone? We can't wait! Pop over to see us at booth 7 and tell us about your data management woes. And you'll get the chance to win a bottle of fine Scotch! 😀 We look forward to seeing you there...
Gilbert and his kids built this big guy on his extra day off work this week... Excellent work! #Formedix #4DayWeek #workweek #3dayweekend
Time is passing really quickly and it'll soon be time for #PhUSE US Connect in Orlando. 😀 We're hoping you'll pop along to booth 21 to chat to us about how we can help you get your clinical trials up and running, and to submission faster!! 👍 https://t.co/LXJ2YbCXSh
Formedix is an all-in-one fully integrated platform to design and build your clinical trial – without any coding knowledge.
Made for pharmas, biotechs and CROs, the Formedix metadata repository and clinical trial automation software makes it quick and easy to find, manage, reuse and share your metadata. The result? You can design, build and submit your trials much faster than before.