4 Comprehensive Training Package on Best FDA 510(k) Process for Medical Devices - Research and Markets

DUBLIN--()--Research and Markets has announced the addition of the "4 Comprehensive Training Package on Best FDA 510(k) Process for Medical Devices" webinar to their offering.

Many companies planning to pioneer a new medical device to the US market need to accede an application to the FDA called a 510(k). The 510(k) submission is needed for all Class I, II and III devices.

To accelerate the procedure of driving a product to market through the 510(k) program, it is obligatory the medical device manufacturers understand the 510(k) procedure, recent trends, actionable strategy, submission and FDA clearance so that you can proactively try to facilitate the FDA review process leading to a prompt clearance.

This pack will provide an opportunity to get accustomed with an FDA's process to interface with the industry early in the process for justifiable 510(k) preparation and submission.

CD/Recorded-How It Works:

- Webinar CD/Recorded will have a series of modules. Our experts have delivered the modules using PowerPoint Presentations.

- Webinar Recording Link or CDs are licensed to be used multiple times at any location with multiple attendants, as you wish.

- Recording links will be valid up to 6 months with unlimited access and reference materials will be mailed to your registered e-mail.

- Free shipment of CDs within 72 hours from the date of purchase and reference materials will be mailed to your registered address.

Webinar Topics:

- 510(k) Submission: Contents and Format for Medical Devices

- 510(k): How To Navigate Through Hurdles And Get It Cleared

- 510(k): Regulatory and Technical Requirements Compliant with eCopy and RTA Policy

- 510(k): Submission and Clearance

Who will benefit?

These webinar will be beneficial to the following:

- Regulatory Affairs Managers

- Directors and VPs

- Clinical Affairs Managers

- Directors and VPs

- Quality Managers

- Directors and VPs

- Sales and Marketing Managers

- Directors

- and VPs

- Complaint Handling and Risk Management Managers and Directors

- Senior and Executive Management

- Compliance Officers and Legal Counsel

- R&D (Engineers

- Scientists

- Managers

- Directors or VPs)

- Product and Development (P&D) Managers

- Directors and VPs

- Site Managers

- Directors

- and Consultants

- Anyone interested in learning about 510(k) process and submission.

For more information visit http://www.researchandmarkets.com/research/xxt2x2/4_comprehensive

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Sector: Professional Development and Training, Medical Devices, Pharmaceutical Packaging

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Sector: Professional Development and Training, Medical Devices, Pharmaceutical Packaging