This webinar will provide valuable assistance to all regulated companies that use cell or tissue based laboratory practices, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. This webinar will describe and show applications of GCCP which can be used in vitro assays to increase quality standards in the laboratory environment.
A result of the initiative to reduce the use of animals for nonclinical safety testing, in vitro alternative methods have become more prevalent to evaluate the safety and toxicity of chemicals, pharmacologicals, biologicals and medical devices. GCCP practices have been proposed by ECVAM to help insure harmonization, standardization and rationalization of cell and tissue culture laboratory practices.
This talk will describe and show applications of GCCP which can be used in vitro assays to increase quality standards in the laboratory environment. The basic principles of the ECVAM Task Force will be discussed as well as other expert opinions on GCCP. A sample SOP for GCCP principles will be provided.
ECVAM Task Force Overview.
The GCCP initiatives.
The basic objectives of GCCP.
How to identify areas of improvement within your in vitro studies?
How to assess the risk and establish best practices?
5 simple process to implement for any in vitro study.
Integration to GLP and GMP regulations.
Present a sample SOP for GCCP’s.
A result of the initiative to reduce the use of animals for nonclinical safety testing, in vitro alternative methods have become more prevalent to evaluate the safety and toxicity of chemicals, pharmacologicals, biologicals and medical devices. GCCP practices have been proposed by ECVAM to help insure harmonization, standardization and rationalization of cell and tissue culture laboratory practices.
This talk will describe and show applications of GCCP which can be used in vitro assays to increase quality standards in the laboratory environment. The basic principles of the ECVAM Task Force will be discussed as well as other expert opinions on GCCP. A sample SOP for GCCP principles will be provided.
Areas Covered in the seminar:
What are GCCP’s?ECVAM Task Force Overview.
The GCCP initiatives.
The basic objectives of GCCP.
How to identify areas of improvement within your in vitro studies?
How to assess the risk and establish best practices?
5 simple process to implement for any in vitro study.
Integration to GLP and GMP regulations.
Present a sample SOP for GCCP’s.
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that use cell or tissue based laboratory practices, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:- Study Investigators of cell or tissue based practices assays
- Supervisors of cell or tissue culture based laboratories
- Study Directors of GLP studies
- QA Managers and Personnel
- Project Management
- Consultants
- Training
- Quality System Auditors
Course Provider
Ann Wright,
