As the leading service provider of Structured Product Labeling (SPL) solutions and XML specialists, Reed Tech is always looking for ways to assist Life Sciences manufacturers with their drug label data. We go beyond SPL to offer XML solutions for electronic submissions, including the latest FDA mandate for prescription drug sample distribution submissions as outlined in ACA Section 6004.
For eight years, Reed Tech has worked closely with the pharmaceutical industry and the FDA as a member of the Health Level 7 (HL7) working group. Our staff actively participates in the HL7 SPL Working Group Leadership, Technical, and Process teams, as well as on the Generics, Biologics, OTC, eDRL, and Medical Device subteams.
Reed Tech has converted over 23,500 SPLs for more than 650Life Sciences manufacturers. With our ISO 9001:2008-certified SPL processes, we optimize the balance between automation and human expertise to ensure the highest degree of quality and efficiency for your drug labeling conversions and content lifecycle management.
The signing into law of the Patient Protection and Affordable Care Act (ACA) in March, 2010 held many ramifications for the Life Sciences and Healthcare industries. While some of the new policies and requirements mandated by ACA came into immediate…
Reed Tech's services have been the right solution at the right time for our business.