Important Dates


  • Deadline of Early-bird Registration:
    Jan. 9, 2015


  • Deadline of Regular Registration:
    Jan. 26, 2015

 

 

Latest News

[2015.01.29]
Information for the media round table (5 Feb) is now available at here!

[2015.01.27]
If you missed the regular registration deadline, you can still register on-site.

[2015.01.09]
ARC welcomes the Asia Pacific Economic Cooperation (APEC) as a new partner!

[2014.12.25] 
Deadline of early-bird registration has be extended to Jan. 9, 2015!

[2014.12.24]
Please refer to the speaker list

[2014.12.2]
On-line Registration is now open! Register Now

[2014.11.25]
Check out the latest Scientific Program


 
 

Welcome message to ARC 2015

Dear Colleagues,

We welcome you to the 8th Asia Regulatory Conference online registration platform.
For those of you interested in diving deeper and getting better insights on what’s at stake for “Advancing Best Practices for Regulatory Review and Submission in Asia,” we warmly welcome you to Taipei, on 4-5 February 2015. The venue will take place in Taipei International Convention Center (TICC).
Asia Regulatory Conferences have constituted over the years a leading forum for dialogue and expertise-sharing on regulatory issues in Asia. We are pleased to offer for this 2015 edition a two-day program to stimulate the debate on recent advancements and challenges faced in Asia in the development of convergent regulatory review and submission processes.

Stakeholders active in the regulatory arena will be invited to exchange views to explore future directions so we can ultimately all together contribute towards reaching regulatory convergence and improvement of quality, safety, and efficacy of medicines in Asia.
This year’s edition will attract stakeholders from regulatory, pharmaceutical, academic, civil society, international and non-governmental organisations, including policy experts from Asia. They will gather under one roof to present the core regulatory policies and other success factors that will facilitate and accelerate delivery of innovative therapies to patients. We believe that valuable insights can be drawn from comparing these factors and that the various panels offered can further encourage the use of efficient and pragmatic regulatory practices for the betterment of regulatory processes and systems in Asia.
We look forward to meeting you in Taipei and to hearing your take on latest progress made in regulatory convergence in Asia.

 

Sincerely yours,

Li-Ling Liu
Director, Division of Medical Devices and Cosmetics

Mike Ward
Chair, Life Sciences Innovation Forum’s Regulatory Harmonization Steering Committee

Barbara Lopez Kunz
Global Chief Executive


Chih-Ping Yang
President

Tadaharu Goto
Director General

Eduardo Pisani
Director General


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