Product Recalls Forum Herndon, Virginia, USA 21-22 May 2018

Description:
This event is designed for pharmaceutical, biotech and medical device professionals with responsibilities in the following areas: - Product Recalls - Patient Safety - Product Safety - Product Quality - QA/QC - Postmarketing Surveillance - Quality Systems and Engineering - Quality Compliance and Audits - Complaint Handling - Medical/Consumer/Regulatory/Clinical Affairs - Product Complaints - Compliance - CMO Management - Business Support Coordination - Product Surveillance - Clinical Operations - Quality Compliance - QA and Supply Integration - Global Device Coordination This conference is also of interest to: - Drug Safety and Complaint Software Companies - Consulting Firms To this: Each year, the number of drug and medical device increase on the market and so does the number of recalls.

Urls:

Brochure:https://go.evvnt.com/186644-1?pid=4440
Booking https://go.evvnt.com/186644-2?pid=4440

Price
Early Bird Pricing - Conference Only - Register by April 6, 2018: USD 1895
Standard Pricing - Conference Only: USD 2095
Onsite Pricing - Conference Only: USD 2295

Speakers: Maureen M. Bernier, MME, PE Biomedical Engineer, Recall Coordinator, FDA, Pearley Bhambri Senior Director Global Quality Systems and Post Market Surveillance, HILL-ROM, Joe Falvo Senior Manager: Postmarket Risk Management, ORTHO CLINICAL DIAGNOSTICS, Noel Gaule Head of Product Quality Surveillance, QP, SHIRE, Jennifer Judge Post Market Compliance, Regulatory Affairs, WELCH ALLYN, Ravi Kalyanaraman, Associate Director.

Time: 8:00 am - 3:00 pm