Taiwan Hosting Medical Device Conference June 1st

May 25th, 2006 Justin Barad News

If you just happen to be in that corner of Asia, you might want to check out this conference on medical devices in Taiwan:

With a focus on the rapidly expanding home-care medical devices sector, Taiwan’s Industrial Technology Research Institute (ITRI) will host an international forum in Taipei on June 1 — the 2006 US-Taiwan Medical Device Technology Commercialization Conference.
The conference will examine global trends, business models, and investment opportunities, with speakers to include Dr. Karen Talmadge, co-founder of Kyphon, inventors of an innovative vertebrae restoring technique they call ‘balloons for bones’; Dr. Tony Chou, head of Abbott Vascular Devices; and Dr. Peter Fitzgerald, the director of the Center for Cardiovascular Intervention at Stanford University Medical Center.
According to ITRI’s new Medical Electronics and Device Technology Center (MED), the conference is intended to serve as a platform for participants from a wide range of sectors to explore collaboration opportunities and spark creative discussion. Around 200 international and domestic attendees are expected to attend.

Keep an eye out for exciting medgadgets coming out of Taiwan.
Read more here…

Upcoming conferences

october

18octallday19alldayWorld Congress on Polycystic Ovarian Syndrome and Fertility, 2018Abu Dhabi, UAE

18octallday19alldayManaging Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an InspectionMinneapolis, MN, USA

Event Details

Post-Market activities, Complaint Handling, MDRs, and Recalls are expensive, time consuming, and often lead to more serious financial consequences. Over 80% of FDA Inspection target observations for lack of compliance in these areas.

By attending this seminar, you will discover:

How to overcome one of the biggest obstacles device manufacturers face
How the FDA expects you to develop and implement proper handling of complaints reportable or non-reportable, product complaint handling and documentation
How and when to file Medical Device Reports (MDR), effective and appropriate communication with the appropriate regulatory agencies in the event of a recall.
How to conduct a correction and removal actions to avoid a recall crisis, including required recordkeeping, expectation from FDA and other regulatory agencies in the event of a recall and key factors in implementing and maintaining compliance with the regulations and real life experiences of FDA.

**New course materials have been added, updated content will include:

Creating Standard Operating Systems (SOPs) for Post-Market Quality Systems and
What to expect from the changes in ORA with Inspection Structure Realignment

This Seminar will have you stop spinning your wheels with nonessential activities, and leave you with a comprehensive learning package that only Rita Hoffman, a former FDA CDRH Recall Branch Chief with experience across the device, drug and veterinary industries can provide.

Spend one and a half days in an interactive course led by Ms. Rita Hoffman, Former FDA CDRH Recall Branch Chief with over 36 years with FDA and leading Industry Expert, who will provide the participants with tools to minimize risk of regulatory enforcement actions.

Time

october 18 (Thursday) - 19 (Friday)

Organizer

Compliance Online 80068SEM

Learn More

Calendar GoogleCal

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18octallday19alldayBiology and Pathology of Infectious Disease Conference, 2018Helsinki, Finland

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22octallday23alldayInternational Conference on Breast Cancer, 2013Vancouver, British Columbia, Canada