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WEBINAR: Medical Devices Registration at an International Level

Regulatory strategy and steps for medical device market access with an eye on the Americas, the Asian pacific Region and China


3 - 4 - 10 June 2020





WEBINAR: Medical Devices Registration at an International Level

The regulatory process from product design to market entry on a global scale is a complex endeavor for medical device professionals. Particularly for small and medium sized businesses it is a challenge to get an overview of the diverging market authorization pathways that differ considerably from the European Union (EU) approval pathway.

This one-day course gives participants an overview how to plan and implement international Medical Device Registration from a European regulatory perspective. The participants will be given insight on the regulatory and quality system strategy, product registration and local agent requirements in major device markets in the Americas, the Asia Pacific Region and China.

Delegates will acquire key competences in international medical device registrations and learn from hands-on industry practice. The webinar will cover both initial market access as well as life cycle requirements and quality system implications.

Module 1: Regulatory strategy & the Americas (3h)

  • Considerations to control market authorization assets
  • Preparation & post approval considerations
  • Impact of the Medical Device Single Audit Program - MDSAP
  • Canadian Medical Devices Regulations overview and update
  • Brazil:  ANVISA and INMETRO requirements and market access steps
  • Overview on the registration in Argentina and Mexico 

Module 2: China (2h)

  • China National Medical Products Administration (NMPA) responsibilities and structure
  • Overview on Laws, Regulations and Guidelines
  • Approval steps and timelines for high risk products
  • Practical experiences. What I should have done differently

Module 3:  The Asia Pacific (1h)

  • Taiwan FDA (TFDA) registrations
  • Singapore Health Science Authority (HSA) approvals
  • Malaysia Medical Device Authority pathway
  • Indonesia NA-DFC requirements

Webinar Language
The webinar will be in English

Arkan Zwick
Arkan Zwick Corporate Regulatory Affairs Director at CROMA Pharmaceutical, Austria

Mr. Arkan Zwick is the Corporate Regulatory Affairs Director of CROMA Pharmaceutical, Austria. CROMA is a private global pharmaceutical and surgical company with products in ophthalmology, orthopedic and aesthetic dermatology. With more than eleven years of regulatory professional experience Arkan´s role includes regulatory advocacy for drug, medical device, combi products and cosmetic compliance projects as well as in house legal advice for contract management, merger and acquisition, and intellectual property projects. He is responsible for the company’s regulatory compliance in the EU working with several notified bodies and for global market authorizations in the Americas and Asia-Pacific.
Arkan has a master’s degree in Law from the University of Vienna and a PhD in European Law. His expertise includes in house legal and regulatory consulting as well as lecturing at the University of Applied Sciences in Vienna and scientific board member and speaker on life cycle conferences and trainings. He is fluent in English, German and French.

This course is addressed to professionals in Medical Device companies with an international market perspective: Regulatory Affairs; Clinical Operations, Quality Assurance, Project Managers, Sales and other departments involved in international market access.

Participant experience

No previous experience in international medical devices registration is needed. Experience with medical devices regulatory processes in Europe may be helpful.

3 Modules
Case studies


Webinar online - 3 modules

June 3rd, 2020             2:00 – 5:00 pm CEST
June 4th, 2020             2:30 – 4:30 pm CEST
June 10th, 2020           2:30 – 3:30 pm CEST

After the registration, you will receive all details about the connection.

The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.

Certificate of attendance

Early Bird: € 610,00* (until 13 May 2020)

Ordinary: € 685,00*

Freelance - Academy - Public Administration**: € 366,00*

for Italian companies: +22% VAT

**Early Bird discount not applicable to Freelance – Academy – Public Administration fee

The fee includes: tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.

Register now

Course Price

685.00 €

Early Bird

Wednesday, May 27, 2020

610.00 €

Payments accepted

  • Bank Transfer
  • Credit Card
  • PayPal

Other Details


3 modules lasting in total 6 hours

Course Type

Limited number of participants

You will receive

Certificate of attendance

At the end of the training, you will be able to

  • Develop an effective strategy to obtain product approvals on a global scale

  • Design robust medical device registration steps in the Americas, Asia Pacific and China

  • Get insight on latest developments

Participants' Feedbacks

Good atmosphere in the group and interaction with the lecturers (really available for all questions)

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WEBINAR: Medical Devices Registration at an International Level

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Terms & Conditions

The fee includes: tuition, teaching materials, lunches and coffee breaks, organizational office assistance, attendance certificate. Early Bird discount not applicable to Freelance – Academy – Public Administration fee.
The course will proceed with a minimum of 8 participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
For further information please contact:  e-mail:  telephone: +39 (0)35.515684

The fee includes: seat at the conference, copy of presentations of Speakers who allow the distribution, informative literature for the day, networking lunch, coffee break, organisational office assistance, certificate of attendance. For further information please contact:  e-mail:  telephone: +39 (0)35.515684

The fee includes: tuition, teaching materials, organizational office assistance, attendance certificate. Early Bird discount not applicable to Freelance – Academy – Public Administration fee. For further information please contact:  e-mail:  telephone: +39 (0)35.515684

Common Terms & Conditions

Terms of payment
Payment should be made online (by credit card) or by bank transfer, at the time of registration (only for Italian companies: + 22% VAT) to EasyB s.r.l by bank transfer or by credit card. Bank transfer payable to:

EasyB S.r.l.
Via Roma, 20 – 24022 Alzano Lombardo (Bergamo)
VAT: IT03633040161
BANCO BPM – Filiale di Carobbio degli Angeli
IBAN: IT81 F 05034 53960 000000003450

Confirmation of event admission will be given on receipt of payment. Invoice will be sent following receipt of payment. EasyB reserves the right to refuse late registrations or additional registrations above the maximum accepted number of participants or registrations of roles that are not included in the target of the event.

Please note that refunds (50% refund of the registration fee) will only be given if cancellation is received at least four weeks before the event date. Cancellations will only be valid if made in writing. Transfer of registrations (or name changes) are allowed for free and should be made in writing within 7 days prior to the event. EasyB reserves the right to postpone or cancel an event, to change the location of an event or to alter the advertised speakers for an event, to change its performance from residential to webinar/online. EasyB is not responsible for any loss or damage as a result of substitution, alteration, postponement or cancellation of an event due to causes beyond its control including without limitation, acts of God, natural disasters, sabotage, accident, trade of industrial disputes, terrorism, hostilities, epidemics, pandemics, and / or authorities’restrictions (so-called factum principis).

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