|Quantity Discounts||1 - 9999|
|1 - 9999|
|1 - 9999|
|1 - 9999|
The FDA has proposed policing only those apps that use supplemental attachments to transform a mobile platform into a medical device and others that act as accessories to an already regulated medical device.
But this growth and the FDA’s definitions have created a quagmire for the FDA and industry. Questions abound:
Approved and in-development device apps are announced every day:
But will all of these need FDA approval? How long will it take, and how much money will it cost, to manage the FDA approval process? If you have questions, we have answers.
Featuring four speakers focusing on the trends, FDA regs, best practices for getting approval and expanding apps into the clinical setting, this virtual conference will provide a detailed look at the emerging market for medical device apps.
Attendees will come away with ideas on how to transform their traditional devices into apps, a better understanding of what needs FDA approval and lessons learned from a firm that already has an FDA-approved app on the market.
Get answers to your toughest questions — in just a day. No travel required. Gather your colleagues for the best, and most cost effective, training in the industry.
This is your invitation to log on Thursday, Aug. 30, and discover what’s really necessary to develop an FDA-compliant medical device application.
Your virtual conference chairperson is Tim Gee, principal and founder of Medical Connectivity Consulting and a principal consultant with Santa Rosa Consulting. Mr. Gee has more than 25 years of experience working with providers and manufacturers on workflow automation through the integration of medical devices with information systems and enabling technologies.
Mr. Gee, along with other top professionals, will teach you:
The virtual conference is convenient to attend. All that’s required is that you be in front of a computer monitor at the appointed time, whether you’re at the office or telecommuting from your office-in-home.
Of course, the panel of experts will be on hand to answer all of your questions. Simply submit your questions via email, and you’ll have answers by the time the session ends.
Everyone in your organization with a role in product development, legal and regulatory affairs will benefit from taking part in this event — and they can do so at a cost that won’t break the budget. You pay a single low registration fee per facility, regardless of how many participate. So spread the word.
Sign up for Medical Device Mobile Apps: What Needs FDA Approval today.
Here’s How It Works
Twenty-four hours prior to Virtual Conference Wednesday, attendees will receive all presentations.
Then just log on to the Virtual Conference website and dial a toll-free number, both provided in your registration confirmation. And relax. That’s all there is to it.
Key people throughout your company will benefit from taking part in this event. Best of all, everyone can do so at a cost that won’t break the budget. You pay one single low registration fee per facility, regardless of how many participate. So spread the word.
The subjective nature of import holds means you may have a different experience at Entry Point A than at Entry Point B, C, or D. If your shipment lands on a day when an inexperienced Customs or FDA person is in charge, it could be a very bad day indeed.
Don’t take unnecessary risks. Sign up today for this timely learning event.
Stress-free! No airport security hassles, no 4 a.m. wakeups, no anonymous hotel rooms. You never even leave your building — not even your own desk.
Interactive! Constant opportunities to ask questions and get involved. Send in queries via e-mail ... you’ll have answers before you log off.
Up-to-the-minute! Every speaker operates in the real world, in real time. If news breaks on Virtual Conference morning, you’ll hear about it before the session ends.
Great value! Spread the word! There’s no limit on number of attendees per site. One low registration fee covers them all. Or register three or more locations for deeper discounts still. Get details here
Meet Your Instructors
Brad Thompson, Member, Epstein Becker & Green; General Counsel, mHealth Regulatory Coalition
Kyle Peterson, Director, Regulatory & Corporate Affairs, Calgary Scientific
Tracy Rausch, Chief Technical Officer, DocBox
Tim Gee, Principal, Medical Connectivity Consulting (Chairperson)
|Date:||Sept. 3–21, 2012|
|Location:||Your office or conference room (no need to travel!)|
Send Your Team for Maximum Benefit
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600
We accept American Express, Visa and MasterCard. Make checks payable to FDAnews.
Or, register by phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600
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