pharmaceutical industry document conversion experience label conversions spl labels
pim compliant documents regulatory affairs

Home > Pharmaceutical Services > Experience

Experienced and Qualified

Reed Technology has the experience, qualifications and capacity to perform your label conversions at the highest levels of accuracy and quality, whether you have one label or hundreds.

Reed Tech's pharmaceutical industry document conversion experience includes successful conversion of over 2,000 SPL labels to date, including Physician Labeling Rule (PLR) conversions.  Reed Tech is also a leading provider of both SPL and SPL-PLR consulting services. 

Our customers include 6 of the world’s top 10 largest pharmaceutical manufacturers, some with over a hundred labels.  Our customers also include smaller firms, each with a single label to manage.  This experience benefits pharmaceutical manufacturers who will be providing PIM compliant documents in the future.  No matter the volume of your need, Reed Tech has the knowledge, experience and resources to provide quality results.

You most likely already know of Reed Tech, even if you do not know us by name.  For over 37 years, we have been performing high-volume, high-accuracy conversions of patent applications and patent grants to XML for the U.S. Patent and Trademark Office (USPTO) and other customers. We deliver over 400,000 XML-converted documents to the USPTO annually. The XML- and image-based patent information products that we deliver to the USPTO are used by USPTO examiners and staff internally and disseminated worldwide. 

Reed Tech is a business unit of Reed Elsevier, one of the largest publishers and information solution providers in the world.  We are a sister company to  Elsevier, a world leader in technical, scientific and medical data aggregation and publication.

ISO Certified

Reed Tech is an ISO 9001:2000 certified company.  Reed Tech optimizes the balance between automation and human expertise to ensure the highest degree of conversion, content management, and scanning quality and efficiency.

HL7 Membership

Reed Tech is dedicated to furthering our knowledge and understanding in order to help our customers to improve their content management practices.  As part of this commitment, Reed Tech staff are members of Health Level 7 (HL7) and participates in the HL7 SPL working group Technical and Process teams as well as the Generics, Biologics, OTC and Medical Devices and the Veterinarian Drug Interest Group (VDIG) Sub-Teams and the HL7 Regulated Product Submission (RPS)

Other Industry Memberships

Reed Tech staff are members of the Drug Information Association (DIA) and the Regulatory Affairs Professionals Society (RAPS).

We're not done until you are!

One of the main reasons the USPTO has chosen Reed Tech, for the last 37 years, is our dedication to their success.  For our pharmaceutical customers, our philosophy is the same: we are not done with our job until you you are done with yours.  For example, your SPL labels must meet your expectations and fully comply with FDA requirements before our job is complete.

Contact Reed Tech for more information

Please contact Ben McGinty, for more information about  conversion and content of label management services for the pharmaceutical industry

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




regulatory affairs

"I have never had a problem with something I submitted not being met by the deadline provided.  Questions are met with a quick and accurate response."
-
Associate Labeling Specialist

Member of Health Level Seven (HL7)

"HL7" and "Health Level Seven" are registered trademarks of Health Level Seven, Inc.

 

structured product labeling services structured product label conversion services structured product label consulting services spl services spl conversion services spl consulting services pim conversion services pim consulting services