Showing posts with label exhibits. Show all posts
Showing posts with label exhibits. Show all posts

Tuesday, September 17, 2013

6th DIA China Annual Meeting - Save the Date!

6th DIA China Annual Meeting

May 11, 2014: Pre-conference Workshops
May 12-14, 2014: Conference, Exhibition and Posters
Shanghai International Convention Center (SHICC), China

Delegate Participation Profile at 5th DIA China Annual Meeting

Showcase Your Products and Services!

Want to select a good booth location and maximize your exposure at 6th DIA China Annual Meeting? Make your reservation today!

Exhibition: Three classes of 3M x 3M booths are available based on booth location:
Floor Plan Application Form_EN Application Form_CN

Booth Size Price (RMB)
3M X 3M Class I 41,000
3M X 3M Class II
3M X 3M Class III
38,000
36,000


Advertising: Application Form_EN Application Form_CN

Type (CMYK) Price (RMB)
Full Page 10,000
Half Page 5,000
Centerfold/Center Spread 18,000
Inside Front Cover 15,000
Inside Back Cover 15,000


Hosting Opportunities: Application Form

In addition to the Platinum, Gold and Silver support levels, additional hosting opportunities include a networking reception, VIP dinner, tea break, lunch and internet booth.

NEW!

6th DIA China annual meeting also provides new hosting opportunities, such as attendee bag insert, hanging banners, and carpet clings offering unique levels of exposure for your company!

For more information, please contact Jean Xu at jxu@kellencompany.com, Sofie Peeters at speeters@kellencompany.com, or call +86 10 5923 1096

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Monday, March 4, 2013

Show what your company has to offer at 4th Pharmacovigilance Conference in Bangalore

4th Pharmacovigilance Conference | New Insights into Current Pharmacovigilance Challenges | March 8-9 | Bangalore, India
Show what your company has to offer
Showcase you company’s product or service and network with industry professionals at the
4th Pharmacovigilance Conference in India.

The two-day conference, to be held in Bangalore from March 8-9, brings together pharmacovigilance, clinical research, medical information, and regulatory professionals and academia to discuss the latest global challenges in drug safety.

Your company can exhibit with a tabletop display and receive one complimentary full-meeting registration and one exhibit personnel registration.

Or become a Platinum Level Supporter and receive three complimentary full-meeting registrations, three exhibit personnel registrations, and exclusive branding and promotion opportunities.

Click here for further details and apply today.
Other events
of Interest
Download the India Calendar of Events
6th Regulatory Conference | April 5-6, 2013 | Ahmedabad, India
5th Annual Meeting | DIA CHINA 2013 | May 12-15, 2013 | Beijing, China
Conference Highlights
  • Updates on recently released GPvP Modules by EMA
  • Japanese model of EPPV – a way forward for other Asian countries
  • Challenges in authoring PSUR for generic manufacturers
  • An insight into Drug Induced Liver Injury (DILI)
  • Global regulatory compliance: challenges and the way forward
  • Safety regulations in emerging Middle East region
  • Efficient management of literature searching
  • Enhanced productivity and quality through process re-engineering; case studies
  • Global outsourcing trends in PV – Indian potential and challenges by China, Taiwan, and Latin America
  • RSI management – best practices to safeguard against pitfalls
  • Attrition and manpower stability; KPO perspective
  • Technology-watch against safety hazard of spurious and adulterated drugs
  • Training; A Formality or a Reality – an industry insight
  • Panel discussion: compensation for trial related injuries
This Pharmacovigilance Conference is perfect for professionals with experience in clinical safety and who are involved in:
  • Pharmacovigilance
  • Clinical research
  • Risk management
  • Compliance
  • Medical information
  • Regulatory affairs
  • Academia
  • Pharmacology
To know more, contact Manoj.Trivedi@diaindia.org
Thank You to our Media Partner
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Wednesday, January 30, 2013

Session Highlights at EuroMeeting2013 - 4-6 March in Amsterdam


Session Highlights at the EuroMeeting 2013
Among the packed conference programme of the EuroMeeting are a few sessions, that you definitely don't want to miss. Hot topics, presentations delivered by high level speakers, and the opportunity to discuss current issues with fellow professionals and our special presenters.
Opening Plenary: Public/Private Partnerships – Working Together in the Interest of Patients
4 March | 14:00-17:15
Public-private partnerships (PPP) are collaborative relationships that transcend national boundaries. Each partnership brings together at least a corporation or an industry association and intergovernmental organisations to achieve a shared health-creating goal on the basis of a mutually agreed division of tasks. The positive aspects and concerns of these initiatives will be discussed.
Moderator:
Steffen Thirstrup, Head of Division, Medicines Assessment and Clinical Trials, Danish Health and Medicines Authority, Denmark

Panelists:
Jan Geissler, Director, EUPATI, Belgium
Kemal Malik, Head of Global Development, Member of the Bayer HealthCare Executive Committee and Chief Medical Officer, Bayer HealthCare Pharmaceuticals, Germany
Pat O’Mahony, Chief Executive, Irish Medicines Board, Ireland
Luca Pani, Director General, Italian Medicines Agency (AIFA), Italy
Andrzej Rys, Director of Health Systems and Products, European Commission, EU
Harpreet Singh, Managing/CSO, Immamics Biotechnologies, Germany

Sessions 1803/1804: GCP Hot Topics
5 March | 14:00-17:30
Session Chairs
Gabriele Schwarz, Head, GCP Inspection Services, German Federal Institute for Drugs and Medical Devices (BfArM), Germany
Beat Widler, Senior Partner, Widler & Schiemann, Switzerland

The GCP Hot Topics Sessions that in recent editions of the EuroMeeting have been bringing together regulators, industry, CRO and academia professionals who want to get first hand information on newest trends, has by now become a EuroMeeting tradition.

In 2013 the impact of changes and evolutions in technology on the conduct and quality management of clinical trials determine the programme of the GCP Hot Topic session. The focus will be on electronic health records (EHRs) when used as source documents or direct input source into clinical trial databases. As a second topic the session will deal with the challenges presented to sponsors and CROs when clinical trial activities are outsourced. This topic is not new but becomes increasingly a root cause of major and critical inspection findings. The program will be completed by the presentation of the White Paper on protocol violations that has been authored by the GCP SIAC.
As in other years the roster of international speakers will involve senior representatives from health authorities, industry and CROs. The audience is invited to actively participate in the panel discussions by bringing examples or challenging statements. Delegates can anonymously submit topic-related questions or cases they would like to be discussed by the panel in advance to the session chairs via the DIA.

Session 1805: EMA Roundtable – Scientific Committees United in Diversity
6 March | 9:00-10:30

Session Chair: Hans-Georg Eichler, Senior Medical Officer, European Medicines Agency, EU
This roundtable will discuss how the EU Scientific Committees come together and interact at the European Medicines Agency to foster scientific excellence in the evaluation and supervision of medicines for the benefit of public health, while being enriched by the EU’s many different cultures and traditions.

Session 1207: Regulatory Town Hall Meeting
6 March | 14:00-15:30

Session Co-Chairs: Guido Rasi, Executive Director, European Medicines Agency, EU and Christa Wirthumer-Hoche, Member CMDh, Deputy Head, Austrian Medicines and Medical Devices Agency (AGES), Austria.
At the Town Hall Meeting attendees can put burning questions to experts about these topics:
• Latest views on legislative changes
• Implementation of the new pharmacovigilance legislation
• Transparency
• Drug shortages
• Decision making
• New approaches to licensing
Download the full Conference Programme and read about these, and the 110+ other sessions, the exhibition and other activities the EuroMeeting has to offer. If you have any specific questions, please feel free to contact us.
Make the most of your EuroMeeting Experience - register for a Pre-Conference Tutorial
Monday, 4 March | 09:00-12:30

Showcase your company’s products or services to key decision makers
The exhibition hall is one of the busiest places at the meeting and provides a unique opportunity to interact with professionals from more than 50 countries working in pharma, devices, government, academia, healthcare delivery and other related occupations, together with representatives from patient organisations and much more.
Apply for your Exhibition space today!
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Call for ABSTRACTS: 4th Cardiac Safety Workshop in Japan - Deadline February 28th

4th Cardiac Safety Workshop in Japan | July 11-12, 2013 | Tokyo, Japan
Don’t miss your chance to share knowledge
4th Cardiac Safety Workshop in Japan
July 11-12, 2013 | Ivy Hall, Tokyo

Submission Deadline: February 28, 2013
Author Notification: March 31, 2013

Suggested Abstract Topics:
  • Non-Clinical Safety Pharmacology and Electrophysiology
  • Clinical QT Assessment Study Design, Analysis and Outcome
  • Clinical Cardiac Safety Assessments
  • Peri-Approval and Post-Marketing Cardiac Safety Strategies
To submit an abstract for the DIA Cardiac Safety Conference please go to the DIA website.
The 4th Cardiac Safety Workshop in Japan aims to present its attendees with interactive sessions and presentations that reflect the ever-changing technology and standards in Japan. Topics will include cardiovascular targets and mechanisms, new regulations, CV toxicity and adverse cardiac drug effects.
For inquiries about abstract submission please contact:
Keiko Cambridge, Program Manager
Phone +81.3.5575.2130
Keiko.Cambridge@diajapan.org


PLUS: Exhibiting Opportunities for the 4th Cardiac Safety Workshop
For information contact DIA Japan:
Nisso 22 Bldg. 7F, 1-11-10 Azabudai,
Minato-ku, Tokyo 106-0041 Japan
Tel: +81.3.5575.2130 | Fax: +81.3.3583.1200
email: diajapan@diajapan.org

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