FORUM · Institut für Management GmbH
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Medical Devices in China, India & the ASEAN countries
Medical device registration
in important Asian countries
Prepare for challenging markets now.
Best practice in two days!
2018-12-09 2019-04-10 Hilton Frankfurt Hochstr. 4 60313 Frankfurt +49 69 13380-0 +49 69 13380-6020

Medical Devices in China, India & the ASEAN countries

Challenges and opportunities of the medical device industry in China and Hong Kong, India and the ASEAN countries

This course provides insights and solutions for accessing the very diversified Asian medical device market and will address legal registration, economy and culture.
Your Topics
  • Country, culture and people: A (future) market for medical devices?
  • Current governmental setup, medical device law and regulation
  • Legal challenges for European medical device companies now and in the future
  • Marketing authorisation: registration, licences and local agents
  • Intellectual property rights and patent protection

Aims and objectives

Europe is currently facing a new regulatory framework for medical devices, which seems to imply dramatic changes for the European medical device industry. Meanwhile, the Asian market presents a challenging yet exciting opportunity to foreign and domestic players alike. These are two good reasons for European medical device industries to look at the Asian medical device market.

So do not wait. Act now and join our course!

You will:
  • learn more about demographic and economic key indicators;
  • get closer insights into the different regulatory frameworks for medical devices;
  • understand how to access the medical device markets in Asia in the best possible manner; and
  • network and establish contact with our experts and other participants.

Who should attend
This unique course addresses the needs of employees in the healthcare industry who intend to register, export and manufacture medical devices to or in China, India and the ASEAN countries:

The speakers' first-hand expertise will be of particular benefit to those involved in:
  • business development;
  • regulatory affairs;
  • market access; and
  • export

The course will be in English.
Your speakers
Sundeep Agarwal
General Manager, Compliance & Regulatory Affairs, Datt Mediproducts Private Limited, New Delhi

Miriam Bandinelli
Cisema China Certification GmbH, Planegg

Torsten Führer
PT Implantex Asia Medica, Jakarta, Indonesien

Go forward


India Adds Four Medical Device Types to CDSCO List of Regulated Products

The Indian government will expand regulatory oversight to our additional types of medical devices starting in January 2020.




Hear from our past delegates and sponsors and learn more about the events.


More on our quality criteria

Quality guaranteed!

IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards. An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2016 - 09.2017 produced a result of 1.6 (based on a school grading system of 1-6).