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SPL-PLR Services
The Physician Labeling Rule (PLR) has added numerous challenges to
Structured Product Labeling submission requirements. New content,
new structure and new Highlights information have added a higher
level of complexity to the original SPL creation process.
Since November 2005, pharmaceutical manufacturers have been required
to submit their drug product labeling information to the FDA in an
XML format known as Structured Product Labeling (SPL). The FDA announced that New Drug Applications, Biologics License
Applications and Efficacy Supplements submitted after June 30, 2006
are required to conform to the SPL-PLR format. In addition, all NDAs,
BLAs and Efficacy Supplements approved since June 30, 2001 must
change to the SPL-PLR format during a scheduled 7-year
implementation plan.
Reed Tech offers Highlights
Information Consulting Services to assist sponsors meet
the challenges of the new PLR guidelines and generate
new content. Reed
Tech is teamed with Quadrant
eLabeling Services LLC to provide pharmaceutical manufacturers with
integrated Structured Product Labeling – Physician
Labeling Rule (SPL-PLR) services: conversion
services plus authoring and/or review of Highlights Text.
Contact Reed Tech for more information
Please
contact Ben McGinty, for more information about SPL-PLR Conversion
Consulting services
Ben McGinty
Senior Director, Business Development
bmcginty@ReedTech.com
215-441-6466
Reed Technology and Information Services
Inc.
7 Walnut Grove Drive
Horsham, PA
19044
U.S.A.
215-441-6400
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