SOURCE: EXTEDO

March 14, 2011 08:00 ET

EMA Presents Roadmap at eRA 2011 Europe in Spain Hosted by EXTEDO

eRegulatory Conference Will Take Place April 13 Through April 14, 2011

OTTOBRUNN, GERMANY--(Marketwire - March 14, 2011) - EXTEDO, a key eRegulatory Affairs solutions provider for life sciences firms, announced today that it will be hosting eRA 2011 Europe (formerly called OPENeCTD), an eRegulatory Conference, in Peguera, Majorca, Spain on April 13 through April 14, 2011.

The event this year will focus on recent Electronic Common Technical Document (eCTD) developments, as well as the latest developments in submission management, drug safety, labelling, registration management planning and tracking, and document management.

Leading experts will be speaking on a wide range of topics including EMA's roadmap and vision on Electronic Submission in Europe, How to Manage Registrations, Communicating with Regulatory Agencies and Pharmacovigilance in a New Era.

One of the keynote speakers will be Dr. Hans-Georg Wagner from the European Medicines Agency.

Attendees will benefit from informative presentations, detailed solution demonstrations and comprehensive client case studies from some of the industry's thought-leaders. During the event attendees can network and share experiences with peers, and learn about relevant solutions offered by EXTEDO sponsors in the partner area. There will also be ample opportunity to interface directly with EXTEDO executives during the conference at pre-scheduled meetings or during the planned social events.

For more information on the eRA 2011 Europe, including a detailed agenda and hotel reservations, click HERE.

"We changed the name of the conference since the event this year is covering a wide range of eRegulatory Affairs topics," stated Christian Bohrmann, Vice President of Global Sales and Marketing for EXTEDO. "eRA 2011 Europe is organized around three tracks and features over 30 domain experts."

About EXTEDO

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, Labelling 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.

For more information visit www.extedo.com.

All trade names, trademarks, and service marks are the rightful property of their respective owners.

Contact Information

  • Media Contact:
    Michael Kane
    EXTEDO
    Tel: 1-978-257-2179
    Email: Email Contact