---------- Forwarded message ----------
From:
Barrie Nelson <CDISC@cventmail.com>Date: Tue, Mar 14, 2017 at 3:49 PM
Subject: CDISC Survey on LOINC Use
To: Abel Magalhaes <
magalhaes.abel@gmail.com>
Having trouble viewing this email? Click here to view the web version.
| LOINC Survey | | Effective March 2018, the FDA Data Standards Catalog will include Logical Observation Identifiers Names and Codes (LOINC) as a terminology standard. Any new study starting after the effective date will need to collect and/or report Labs' results with an accompanying LOINC code, where possible. It is important we begin discussions with industry, CRO, academia and other CDISC community representatives on this topic to gauge the current state of awareness and understanding of LOINC and how to apply it to clinical research. Additionally, the community needs to understand FDA expectations to provide data appropriately. We are reaching out to our entire community with a survey to understand your work, if at all, with LOINC. We will bring information gathered to a team of representatives from FDA, NCI, NLM, Regenstrief, and CDISC to discuss requirements, challenges and opportunities with an end goal of providing guidance.
To complete the survey, click this link https://www.cvent.com/d/25qjl0/. Please submit your feedback by 22 Mar 2017.
| | | | Thank you for taking the time to provide us with your important input and partnering with us to Enable Smarter Research. |
| |
CDISC | 401 W 15th Street | Ste. 800 | Austin | TX | 78701 | US | +1 (512) 363-5826
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