8th Clinical Trials Inspection Readiness Summit

Posted By : User Ref No: WURUR35314 0
  • Image
  • TypeConference
  • Image
  • Location Philadelphia, Pennsylvania, United States
  • Price
  • Date 14-08-2019 - 15-08-2019
8th Clinical Trials Inspection Readiness Summit, Philadelphia, Pennsylvania, United States
Conference Title
8th Clinical Trials Inspection Readiness Summit
Event Type
Conference
Conference Date
14-08-2019 to 15-08-2019
Location
Philadelphia, Pennsylvania, United States
Organization Name / Organize By
ExL Events
Presented By
Emily Sternberg
Organizing/Related Departments
Pharmaceuticals
Organization Type
Event Organizing Company
ConferenceCategory
Both (Technical & Non Technical)
ConferenceLevel
International
Related Industries

Medical/Healthcare/Hospital

Location
Philadelphia, Pennsylvania, United States

Clinical trial personnel constantly look for strategies to improve their inspection readiness operations. One of the keys to success involves proactively preparing for inspections to ensure that you are equipped for regulatory oversight at any moment. Another, larger scale practice includes creating a holistic culture within your organization through collaboration, innovation, and thoroughness. The 8th Clinical Trials Inspection Readiness Summit will provide invaluable resources and interactive discussions for attendees to help institute a culture of preparedness within their organization.

URL:
Brochure: https://go.evvnt.com/437680-2?pid=6581

Artists / Speakers: Kristen Bennett Associate Director, Client Delivery, THE AVOCA GROUP, Nancy Bitters Inspection Management Lead, Biopharma, Global Research and Development Quality, EMD SERONO, Jamie Bridges Director, GDMS, Operational Excellence, MERCK, Sharon Brower Director, Training and Process and Continuous Improvement, BRISTOL-MYERS SQUIBB, Linda M. Coleman Director, Human Research Protection Program, YALE UNIVERSITY, Grace Crawford VP Clinical Quality and Compliance, MEDIMMUNE, Christina Deluca Associate Director, GCP Inspection Management, MERCK, Alyssa K. Gateman Associate Director, Yale Center for Clinical Investigations, Director Office of Quality Assurance and Training, YALE UNIVERSITY, Vinita Leslie Director, Trial Master File Process Owner, Regulatory Operations, BIOGEN, Ann McCabe Director, Process Excellence and Risk Management Clinical Development Operations, DAIICHI SANKYO, Lydia Milne Director Quality Systems Inspection Program, ASTELLAS, Julia Moore Associate Director, Clinical Operations, SANGAMO THERAPEUTICS, Laura Naranjo Manager, TMF Operations, DAIICHI SANKYO, Johanna Stamates Executive Director, Research Compliance and Quality Assurance, UNIVERSITY OF MIAMI, Katherine Taylor Director, GCP Inspection Management, MERCK, Ann Taylor Director, Inspection Readiness Lead, Clinical Development Quality, PFIZER, Michele Weitz Senior Director, GCP Compliance Operations, CLOVIS ONCOLOGY, INC., Michael Wieczerzak Associate Director, Clinical Quality Management, EMD SERONO

Time:  8:00 am to 5:00 pm

Registration Fees
Available
Registration Fees Details
Early Bird Pricing — Register by June 28, 2019: USD 1895.0 Standard Pricing — Register after June 28, 2019: USD 2095.0 Onsite Pricing: USD 2195.0
Registration Ways
Email
Phone
Website
Other
Address/Venue
  Sonesta Hotel Philadelphia 1800 Market Street, Philadelphia, United States  Pin/Zip Code : 19103
Contact
Emily Sternberg

[email protected]