ComplianceOnline, the leading GRC advisory network, and leading regulatory expert Dr. David Lim, will conduct a one-and-a-half day, in-person seminar on FDA compliant GLP for non-clinical studies for pharmaceutical and medical device industries.
Online PR News – 04-July-2012 – USA – Palo Alto, CA, USA – June 28, 2012 – ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries. The one-and-a-half day long, in-person seminar, led by regulatory expert and RAPS faculty member Dr. David Lim, will be held on July 26 and 27,2012 in Orlando, FL.
The seminar will help attendees comprehensively understand Good Laboratory Practice (GLP) regulations and achieve compliance. The course has been pre-approved by RAPS and participants will be eligible to receive up to 10 RAC credits toward their certification on completion.
For more information or to register for the seminar, please click here.
Seminar instructor Dr. David Lim is a Ph.D. in biological sciences. He has held various positions at Duke, US National Laboratories, Intrexon Corporation, Terumo, US FDA/CDRH, and EraGen Biosciences, Inc. Currently, Dr. Lim is serving as a faculty at the Regulatory Affairs Professional Society (RAPS) and is an advisor to the Presidents and CEOs of FDA-regulated industry.
During this interactive workshop, Dr. Lim will explain the relevant and applicable US regulations, regulatory requirements and guidance necessary for GLP compliance. This workshop is intended to provide guidance on GLPs for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for pharmaceutical and medical device products for human use regulated by the FDA. On the second day of the seminar, group discussions will be held to understand how GLPs can be implemented.
This course will benefit anyone in FDA-regulated industry, including, but not limited to, handling nonclinical laboratory data and documents concerning animal and human drugs, biologics, biosimilars, medical devices or any combination products thereof. It is particularly useful for those who are engaged in conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for FDA-regulated medical products. This workshop is a must for those who are directly or indirectly involved in nonclinical laboratory studies regulated by the FDA.
Date: Thursday, July 26, 9 AM to 4 PM EDT and Friday, July 27, 8 AM to 12 Noon EDT,
Venue: Orlando Airport Marriott, FL
Registration Cost: $1299 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to firstname.lastname@example.org
For more information on ComplianceOnline or to browse through our trainings, please visit our website.
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,000 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com.