GlobalCompliancePanel

The webinar explains Process Capability Analysis (PCA) and shows how to apply it to various clauses of an ISO 13485. PCA can help you develop, implement, and improve your QMS.

The purpose of the FDA inspection is a verification activity that should demonstrate to the regulatory agency and provide assurance that products consistently meet quality expectations

Class participants will familiarize themselves with the federal laws and regulations enforced by DEA pertaining to Schedules II though V controlled substances that are dispensed, or prescribed by a physician as part of a pain treatment plan.

This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly.

Overview: This webinar will cover the fundamentals of signal detection, and how these can be augmented by the use of data mining techniques.

The webinar will help participants review and understand FDA requirements for OTC Drug labeling and compliance. OTC Monographs and their importance to OTC Drug marketing in the U.S. will also be covered.

This three hour overview of financial risk management will provide the fundamentals to risk management that all managers need to comprehend.

This training will cover several recommendations to improve Due Diligence when distributing Schedules II through V controlled substances and regulated chemicals to your customers and what steps can be taken to prevent

Overview: An overview of the drug development process, reviewing key deliverables for each stage of the development path with a special focus on managing the development process when using external resources such as Contract Manufactures,