\n
Who Will Benefit:
\n\n
This semina
r will provide an overview and in-depth snapshot of the medical device reg
istration and approval process for Japan. Employees who will benefit inclu
de all levels of management and departmental representatives from key func
tional areas and those who desire a better understanding or a "\;refre
sh"\; overview of the medical device registration process\, including:
\n\n
\n - Clinical Research Associates
\n - Clinical Pro
ject Managers
\n - Regulatory Affairs Professionals
\n - Clinical Inve
stigators and Clinical Research
\n - Regulatory Affairs Management
\n - Regulatory Affairs Specialists
\n - Regulatory Project Leads/SME'\;
s
\n - Auditors
\n - Compliance Specialists
\n - Clinical Affairs
\n - Quality Assurance
\n -
Consultants
\n - Distributors
\
n
\n\n
===
\nPlease contact the event manager Marilyn below for the foll
owing:
\n- Discounts for registering 5 or more participants.
\n-
If you company requires a price quotation.
\n- For event ticket\, co
ntact +1 929 900 1853
\nEvent Manager Contact: marilyn.b.turner(at)ny
eventslist.com
\nYou can also contact us if you require a visa invita
tion letter\, after ticket purchase.
\nWe can also provide a certific
ate of completion for this event if required.
\n \;
\nNO REF
UNDS OR TRANSFER ALLOWED ON REGISTRATIONS
\n-------------------------
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\nThis Event Listing is Prom
oted \; by
\nNew York Media Technologies LLC in association
\nwith GlobalCompliancePanel.\n
http://www.NyEventsList.com\n
http://www.BostonEventsList.com\n
http://www.SFBayEventsList.com\n-------
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