marcusevans german conferences

Regulatory Information Management Pharma

XEVMPD und ISO IDMP, eCTD v 4.0, Information Tracking, Pharmakoviliganz, Masterdatenmanagement, Verknüpfung der regulatorischen Tasks

25. - 26. Nov 2013
Westin Grand Berlin, Germany

media partner request
  1. Media and Association Partner Opportunities

    marcus evans events are attended by senior-level executives from leading organizations across all key industry sectors and professions.

    Leverage marcus evans’ exclusive speakers, delegate and sponsor relationships to engage your target audience in an exclusive and focused atmosphere. marcus evans works with associations, companies and bloggers to help them achieve their marketing objectives through various promotional opportunities. These opportunities are custom-tailored to fit your marketing goals, in order to maximize the exposure and impact of the partnership.

    Some of the exposure that media and association partners can expect from a marcus evans event include*:


    Company logo and profile on the event brochure

    • Emailed to all speakers, sponsors, delegates and any potential attendees of the conference
    • Included either in the conference packet or on the delegate tables on-site of the conference

    Company logo and link on the event website

    • Exposure to all speakers, sponsors, delegates and any potential attendees of the conference
    • Emails sent to over 10,000 individuals with a link back to event website
    • Links to the event website placed in various social media campaigns on LinkedIn and Twitter

    Email campaign inclusion

    • Presence (either in text or by logo) on all email campaigns to speakers, sponsors, delegates and potential attendees of the conference
    • Inclusion in a total of 4-5 email broadcasts

    Discount to readers

    • marcus evans can offer a $200 discount on our full-price attendance pass for your members/readers

    Access to conference speakers for interviews

    • marcus evans can provide access to our industry leading speakers for interview opportunities and content development for your website/newsletter/magazine or blog

    Social media campaign

    • Access to our LinkedIn and Twitter channels to help promote your company
    • Option to customize messages based on your marketing goals to a targeted, senior-level audience


    Complimentary attendance pass

    • Publications/websites – one member of your editorial staff can attend on a complimentary basis (airfare and accommodation are not included. Person attending must agree to the press pass policies)
    • Associations – one member of your board or staff can attend on a complimentary basis (airfare and accommodation are not included)

    Onsite materials distribution

    • Option to include your materials in the conference packet or on the delegate tables on-site of the conference

    Table Top Display

    • Option to add promotional materials to our shared media partner table top

    Post-Conference Deliverables
    Attendee mailing list

    • Mailing list will include all direct mailing contact information

    Access to post-conference website

    • Access will include the speaker presentations and materials.
      • Please note: you will need to ask your marketing rep for permission to post or use any of these materials

    *depending on media and association partnership package

    All partners receive full account management to ensure objectives are set, measured and exceeded.

    Please enter required fields: *Required field

  2. Get a new challenge

Conference Speakers

Timm Pauli
Director of Regulatory Informatics and Submission Management
Merck KGaA

Dr. Susanne Braunhofer
Head Regulatory Affairs
Acino Pharma AG

Karl-Heinz Loebel
Head of Regulatory Operations
PharmaLex GmbH

Jrg Schnitzler
Associate Director Regulatory Operations, Regulatory Affairs Europe
Boehringer Ingelheim Pharma GmbH & Co. KG

Dr. Bernhard Wittmann
Sigmapharm Arzneimittel GmbH

Dr. Karsten Goedecke
Regulatory Affairs Manager and Project Manager
Basilea Pharmaceutica International AG

Dr. Andreas Franken
Abteilungsleiter Klinische Forschung / Elektronische Verfahren
Bundesverband der Arzneimittel-Hersteller e.V. (BAH)

Christine Danila-Lersen
Director, Regulatory-, Quality and Safety coordination EEMEA (East Europe, Middle East and Africa) Commercial Operations Intercontinental
CSL Behring AG

Stefan Brgger
Head of Proprietary Information eDiscovery 1, GRA Document Management
Bayer Pharma AG

Petra Gerecke
Leiterin Abteilung Zulassung
mibe GmbH Arzneimittel

Dr. Jrg Stben
Senior Expert Controlled Document Management Solutions
Boehringer Ingelheim Pharma GmbH & Co. KG

Andrew Marr
Former Member of the ISO Technical Committee 215, former Rapporteur of ICH M2 Expert Working and Co-Rapporteur of ICH M2/M5 Joint Expert Working Group, former Director of eRegulatory Development at GSK

Dr. Klaus Geldsetzer
Director Regulatory Intelligence Europe, Chief Compliance Officer Europe
Santen GmbH

Dr. Barbara Rangetiner
Director International Drug Regulatory Affairs
Octapharma Pharmazeutika Prod.Ges.m.b.H.

Dr. Gerd Brker
Group Leader Regulatory Affairs
Salutas Pharma (Sandoz)

Dieter Weiser
Manager Strategic Support, Quality Control
Takeda GmbH

Prof. Dr. med. Helmut Brasch
Direktor Patientensicherheit, Stufenplanbeauftragter, kommissarischer Direktor des Bereichs Medizin
AstraZeneca GmbH

Social Media


General Enquiries

Heide Guhl-Behrendt

Marketing Manager
Unter den Linden 21
10117 Berlin

0049 (0)30 89061 283
Fax: 49 (0) 30 890 61 434