EXTEDO and Asphalion Will be Advising Life Sciences Firms on How to Comply With New European Medicines Evaluation Agency Regulations at Drug Information Association EuroMeeting  
3/19/2012 8:54:36 AM

MUNICH, GERMANY--(Marketwire - March 19, 2012) - EXTEDO, a key Regulatory Information Management solutions provider for life sciences firms, today announced that Remco Munnik and Dr. Gerhard Neurauter, two renowned experts on electronic submission and regulatory data management, will be available to meet with executives from the life sciences industry at the DIA EuroMeeting in Copenhagen, Denmark.

Mr. Munnik is the Regulatory Information Director at Asphalion and member of TIGes. He tracks all global developments that impact electronic submissions. Dr. Gerhard Neurauter is Director of the Regulatory Competence Centre at EXTEDO and the product manager for EURSvalidator. Mr. Munnik and Dr. Neurauter will both be available at the EXTEDO booth (#519) to answer questions about the pharmacovigilance legislation (XEVMPD) announced by the European Medicines Agency (EMA) and about current developments in the Regulated Product Submissions (RPS) project. Meeting times are available on Tuesday, 27 March 2012 from 15:30-16:00 and Wednesday, 28 March 2012 from 10:30-11:00. Conference attendees that would like to meet Mr. Munnik and Dr. Neurauter can sign up at the EXTEDO booth.

EXTEDO life sciences industry experts will be also be demonstrating MPDmanager™, a new software solution that enables companies to manage and submit all regulatory data in the XEVPRM format mandated by the EVMPD legislation.

"The July 2nd deadline to comply with the EMA legislation is just around the corner," stated Tore Bergsteiner, CEO of EXTEDO. "The DIA EuroMeeting provides an excellent opportunity for attendees to meet with two outstanding regulatory experts and get detailed answers to their questions about the new legislation and latest RPS project developments."


EXTEDO is the key software and service solutions provider in the field of Regulatory Information Management. The complete EXTEDOsuite is unique in all that it covers within eRegulatory Affairs: 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 one of the worldwide leaders in each of its areas of operation.

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