International conference details
FDA-Product
The New FDA-Product Approval 2017
Fremont (United States), 12 January 2017
Domain:
Key deadlines
- Conference starts:
- 2017-01-12
Website
Conference Description
Overview:
The US Food and Drug Administration has recently released information about its new strategies as a result of the new administration.
The new commissioner recently announced a new policy for Warning Letters and FDA-483 responses, putting manufacturers under very tight response timelines.
Areas Covered in the seminar:
The "new" FDA organization and mission
Enforcement changes- increased inspection
Enforcement Changes-new expectations
Manufacturers responsibilities for FDA-483s
Manufacturers responsibilities in Warning Letter situations
Pre-market changes-Human Factors
New Risk Management Guidance
Who Will Benefit:
Regulatory Managers
Quality Managers
Product Managers
Project Managers
Speaker Profile:
David Dills , Global Regulatory Affairs & Compliance Consultant, has an accomplished record with more than 26 years of experience within regulatory affairs, compliance and quality consultative services for early-stage/established Class I/II/III medical devices, IVDs, and bio/pharmaceutical manufacturers on the global landscape.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
For full datails & Event Link : http://www.compliance4all.com/control/w_product/~product_id=501066LIVE?channel=mailer&camp=Webinar&AdGroup=confroll_Jan_2017_SEO
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Conference creator: compliance4all
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Conference Location
161 Mission Falls Lane, Suite 216,,
Fremont 94539 (United States)