ComplianceOnline

This 7-hr webinar on Impurities in Pharmaceutical Products will provide a comprehensive overview of impurities which must be controlled in pharmaceutical products and the strategies for controlling them.

This 2-hr webinar on DEA Due Diligence will cover several recommendations to improve the Corporate Due Diligence when narcotic drugs are purchased by their customers.

This 90-minute webinar on black-labeling for cosmetics will show how to prepare and file a request for a monograph of a tradename ingredient.

This 2-hr webinar will cover DEA record-keeping and security requirements that any DEA registrant must comply with when handling controlled substances. It covers elements of what occurs during an unannounced inspection and the auditing methods.

This Green Marketing Claims training will cover FTC's revised Green Marketing Guides and show how marketers can avoid regulatory pitfalls, substantiate their claims and qualify them to avoid deceiving consumers.

In this FDA documentation best practices training for FDA regulated companies, learn the techniques ideas that will help identify effective methods designed to improve your document control systems.

This training on responding to FDA Form 483s and Warning Letters will present methods for reviewing, evaluating, and writing responses to FDA Form 483s and Warning Letters.

This FDA Pre-Approval Inspection training will focus on the purpose and scope of pre-approval inspections, the consequences from them, and keys to a successful FDA pre-approval inspection.

In this CAPA training webinar, we will focus on ideas that will help identify effective methods designed to improve your response to process deviations and help you develop a standardized plan to fully resolve discrepancies so they do not recur.

This Project Management training for FDA Regulated Companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage.