Labcompliance

This web-seminar will discuss how to design, prepare, conduct and document method validation exaperiments for Good Laboratory Practice and Good Clinical Practice studies. Attendes will receive 10+ best practice guides for easy implementation.

This web-seminar will discuss how to use electronic and digital signatures for FDA and international compliance.

This seminar will discuss how to calibrate and qualiy stability chambers for FDA and international compliance.

This seminar will discuss how to validate laboratory computer systems for FDA and international compliance

This seminar will discuss how to apply USP chapter for all laboratory equipment and systems

This seminar will discuss the new risk based approach and attendees will get get real world case studies for testing

This seminar will discuss how to control changes of hardware, firmware, software and documentation of computer systems and netorks

This seminar will discuss how to comply with FDA's ongoing Part 11 inspection program

This seminar will discuss how FDA did change inspection practices and how to respond to avoid 483s and Warning Letters

This seminar will discuss strategies and present examples on what to train, how much to train and how to document effectiveness