GlobalCompliancePanel

This seminar examined the existing and proposed requirements for the FDA's Design History File (DHF) and its derivate documents, the Device Master Record (DMR) and Device History Record (DHR).

This seminar offered in-depth learning on ways by which a firm can define a sustainable structure for its validation program; how Change Control.

NetZealous Successfully completes Seminar by Steven Kuwahara on GMP Compliance for Pharmaceutical Quality Control Laboratories

Seminar in Chicago, IL on November 5 and 6, 2015. This interactive seminar, whose topic was “HIPAA Privacy Security –Time to Get Serious”

HIPAA compliance is a sine qua non for compliance professionals. Of late, HIPAA has undergone several changes to many of its Rules.

GlobalCompliancePanel will hold a RAPS approved two-day, in-person seminar in Philadelphia on the topic, “Applying ISO 14971 and IEC 62304 – A guide to practical Risk Management” on November 7 and 8, 2013 (Thursday and Friday).

2-day In-person Seminar on “Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding Penalties” at Chicago, IL 2013

This seminar relates to issues to consider for complying with ISO 14971, IEC 62304 and IEC 60601-1:2005, the global standards governing regulations and guidelines for software in medical devices.

2-day In-person Seminar on “Effective Complaint Handling, Medical Device Reporting and Recalls” in Boston

This course is designed to provide a microbiology-focused education about all aspects of water systems and how Biofilm manages to thrive there.