GlobalCompliancePanel

The primary objective of this course is to impart to its participants the value of conducting proper root cause analysis as part of an investigation system.

GlobalCompliancePanel, a compliance training gateway, will host a two-day, in-person seminar on the topic, “Good Laboratory Practice Regulations –Introduction and Strategies for Implementation” on March 21 and 22 at Mumbai.

By far, one of the most difficult tasks in getting a lyophilized product from the laboratory bench to the commercial freeze-dryer is scale-up, or cycle transfer.

Every technological innovation brings with it the same share of challenge, as excitement and advantage. Cloud computing is the latest wave to hit the technology sector. It has it unique advantages.

GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, “Verification vs. Validation - Product, Process, Software and QMS” on January 17 and 18 at Las Vegas.

When preparing statistics for Quality Control and Process Validation, professionals are required to compare various sets of data.

This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs.

This webinar is about the FDA's recently instituted annual "Strategic Priorities" initiative, with emphasis on what it has for 2013.

Why does the American healthcare and medical industry need to be in compliance? For the simple fact that such national disasters as mentioned above need to be prevented and eliminated.

The course will introduce the main elements of risk management and the application of risk management principles and requirements to the medical device development cycle.