October 21, 2010 08:00 ET

Harv Martens From EXTEDO Will Be a Featured Speaker at the DIA Electronic Submissions Conference

WEST CHESTER, PA--(Marketwire - October 21, 2010) -  EXTEDO, a key eRegulatory Affairs solutions provider for life sciences firms, today announced that Harv Martens, Vice President of Operations for North America and Japan for EXTEDO, will be a featured speaker at the 9th Annual DIA Electronic Submission Conference being held in San Diego, CA on October 28-29, 2010. 

On October 28th, from 12:00pm to 12:30pm Pacific Time, Mr. Martens will be presenting at a session titled eCTD Tools Interoperability and Compliance Study (ETICS) III. He will also be a panel member that will be discussing Global Electronic Submissions at 3:30pm to 5:00pm Pacific Time on October 28th.

DIA attendees can also view the eCTDmanager Suite™, an all-in-one electronic submission management system for eCTD and non-eCTD electronic and paper submissions at booth number 1. Also on display will be EXTEDO PcVmanager, a drug safety management software solution based on the E2B and MedDRA standards that enables users to classify, create, review, submit, and maintain Pharmacovigilance data and adverse event reports. Additionally, qualified DIA attendees can pick up a free trial version of GECCO, the leading eCTD validation and review tool with over 1,100 users globally.

"It is critical that life sciences firms develop a submissions strategy that can accommodate the various standards that are in place throughout the world," stated Harv Martens, Vice President of Operations for North America and Japan for EXTEDO. "We have been working closely with the various regulatory authorities to ensure that our products will not only meet today's requirements, but will also meet tomorrow's standards."


EXTEDO is the key solutions and services provider in the field of eRegulatory Affairs. The complete EXTEDOsuite is unique in all that it covers: Product Registration Planning & Tracking, Submission Management, Pharmacovigilance Management, Labeling Management, and Document Management.

EXTEDO provides configurable off-the-shelf products, as well as customized and integrated solutions. EXTEDO also provides EURS is Yours, the validation, review and approval system for the EMA and more than 25 Regulatory Authorities worldwide.

Today EXTEDO serves more than 700 customers in 57 countries ranging from small companies with less than 25 employees to large multi-national organizations. EXTEDO operates in the following markets for human, veterinary and crop protection: Life sciences, including pharmaceutical, biotech and biopharma, generics, homeopathics and medical devices, healthcare, and public sector. EXTEDO is recognized as the worldwide leader in each of its areas of operation.

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