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October Biomed/Biotech SIG Meeting
Where
Kelly's Deli Conference Center
Next to the entrance to 7519 Standish Drive
FDA/CVM Center
Rockville, Maryland 20855
When
Oct 8, 2009
6:00 pm - 9:15 pm
Good Clinical Practice (GCP) Concepts for Quality Clinical Trials
Presented by
Jan H.
Pierre, MPH
Principal
Consulting
Quintiles Consulting
and
Quality Assurance in Disaster Recovery
Presented by
Cynthia Smith,
RQAP-GLP
Senior Quality Assurance
Auditor
Bridge Laboratories, Inc.
Thursday, October 8, 2009
6:00 - 6:15 PM: Networking and
Pizza/ soft drink and networking
6:15 - 9:10
PM: Program
9:10 - 9:15 PM: Door-prize
drawing and networking
Open and free to the
public
Location: Kelly’s Deli
Conference Center, 7519 Standish Place,
Rockville, MD 20855
Driving directions from
I-270 (N or S bound):
Take Exit 9A
and exit from the first right exit.
Turn
left (east) onto Shady Grove Dr.
Turn right
(south) onto Rockville Pike (Route
355).
Turn left (east) onto East Gude
Dr.
Turn left (north) immediately onto
Crabb’s Branch Dr.
Turn left (west)
immediately onto Standish Place.
(The first
building on your right side is 7519 Standish
Place; open parking)
The conference room is
on the first floor with its entrance opposite
to the left side of building main
entrance.
For headcount purpose, please register here by Thursday noon, October 8, 2009. For registration problems or further information contact Dr. George Chang, Co-Chair of Biomed/Biotech SIG, at gchang2008@yahoo.com or call 240-793-8425.
Presentation Summaries:
Good Clinical Practice (GCP) Concept for Quality Clinical Trials - This presentation will provide you with a basic overview of today’s clinical trial landscape and the application of GCP. We will examine quality concepts in clinical research, specifically, what does FDA look for when examining the quality and integrity of clinical research studies. Further, could you detect or possibly prevent fraud from happening to you. In addition, you will walk away appreciating the work that biomedical researchers do and the importance of clinical trials.
Quality Assurance in Disaster Recovery - Disasters are happening more frequently and Recovery is taking on a different perspective. This presentation will provide a general introduction to the role of Quality Assurance in Disaster Recovery preparedness. This presentation will address some of the basic requirements when preparing for a disaster as well as identifying areas of concern in a GLP regulated environment. Are you prepared?
Speakers’ Biography:
Jan Holladay Pierre, MPH, currently serves as Principal Consultant with Quintiles Consultants. Ms. Pierre serves as a project resource and the team leader for various bioresearch monitoring projects. Ms. Pierre has more than twelve years of experience working in the clinical research arena, with a unique combination of expertise in inspections, regulatory compliance, auditing, quality assurance, and training. She was an FDA Investigator with over six years of experience auditing/inspecting sponsors, IRBs, clinical investigators, manufacturers, and non-clinical laboratories. Ms. Pierre was also a member of the Foreign Inspection Cadre while at FDA. She has experience as a Site Compliance Director overseeing clinical trial operations; a CRO QA Director responsible for developing SOPs and conducting internal and external audits; and a Regulatory Compliance Director responsible for ensuring clinical trials meet regulatory compliance. She also served as faculty with RxTi, a clinical research training organization. Ms. Pierre holds an M.P.H. in International Health Policy.
Cynthia L. Smith, RQAP-GLP is a Sr. Quality
Assurance Auditor for Bridge Laboratories,
Gaithersburg, MD. She has over 20 years
experience working in the field of GLPs.
Prior to joining Bridge Laboratories, she had
almost 10 years in Quality Assurance at Covance
Laboratories, Vienna, VA, and has held various
positions between the two which include: GLP
Quality Assurance, Training Specialist,
Computer Validation Auditor, and Toxicology
Technician. Ms. Smith has been active in
both the National Capital Area Regional Society
of Quality Assurance (NCARSQA) and the Society
of Quality Assurance throughout her career in
Quality Assurance, and currently holds a
position on the Board of Directors for NCARSQA.
She has attended and conducted numerous
training programs on a variety of topics
including GxPs, Computer Validation &
Electronic Signatures, and Multi-Site studies.
Ms. Smith holds a Bachelor of Science degree in
Animal Science from the University of
Maryland.