Pharmaceutical Compliance Training

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Stay Compliant. Stay Informed

This training provides a concise overview of the AdvaMed Code of Ethics, which governs ethical interactions between medical device/technology companies and healthcare professionals (HCPs).

Suggested For:

• Compliance Officers
• Compliance Teams
• Medical Device Representatives
• Regulatory Affairs
• Legal Teams

Provides an overview of state-specific aggregate spend laws governing reporting and compliance for transfers of value to healthcare professionals. Covers licensing, gift and meal restrictions, pricing disclosures, and detailed state-by-state reporting obligations.

Suggested For:

• Compliance Officers
• Field Based Sales Professionals
• Marketing Personnel
• Transparency Reporting

This module details AKS prohibitions on remuneration to HCPs, safe harbors, and high-risk activities. Participants will review enforcement cases and learn how to structure compliant interactions.

Suggested For:

• Compliance Officers
• Field Based Sales Professionals
• Marketing Personnel
• Regulatory Affairs
• Promotional Review Committees
• Medical Device Representatives

Explains sterile practices for handling equipment and preparing medications to prevent contamination and ensure patient safety.

Suggested For:

• Field Based Sales Professionals
• Medical Device Representatives
• Medical Science Liaisons

Outlines OSHA standards for preventing exposure to bloodborne pathogens, including universal precautions and proper PPE use.

Suggested For:

• Field Based Sales Professionals
• Medical Device Representatives
• Medical Science Liaisons

This training clarifies the role of pharmaceutical companies in supporting independent CME programs. Topics include ACCME accreditation, permissible funding, and restrictions on influencing faculty or topics.

Suggested For:

• Compliance Officers
• Compliance Teams
• Medical Affairs Personnel
• Medical Science Liaisons

Covers the purpose and structure of Corporate Integrity Agreements, including common elements, enforcement, and reporting. Ideal for compliance and legal professionals managing federal healthcare obligations.

Suggested For:

• Compliance Officers
• Compliance Teams
• Legal Teams

This training provides an overview of FDA regulations (21 CFR Part 99) governing the dissemination of information about unapproved/new uses of approved drugs, biologics, and devices.

Suggested For:

• Compliance Officers
• Field Based Sales Professionals
• Marketing Personnel
• Regulatory Affairs
• Promotional Review Committees
• Medical Device Representatives

Provides training on identifying electrical hazards, safety standards, and emergency protocols specific to healthcare environments.

Suggested For:

• Field Based Sales Professionals
• Medical Device Representatives
• Medical Science Liaisons

Explains FDA requirements for electronic records and signatures, focusing on validation, audit trails, access controls, and compliance practices for regulated industries.

Suggested For:

• Compliance Officers
• Compliance Teams
• Field Based Sales Professionals
• Sample Operations
• IT and Data Security
• Legal Teams

Provides an overview of the FCA, including false claim standards, whistleblower provisions, penalties, and its impact on the pharmaceutical industry.

Suggested For:

• Compliance Officers
• Field Based Sales Professionals
• Marketing Personnel
• Medical Science Liaisons
• Regulatory Affairs
• Promotional Review Committees
• Medical Device Representatives

This module outlines JFPA restrictions on unsolicited fax ads, opt-out requirements, and EBR exceptions. State-specific rules and penalties are also covered.

Suggested For:

• Compliance Officers
• Compliance Teams
• Field Based Sales Professionals
• Medical Affairs Personnel
• Marketing Personnel
• Regulatory Affairs
• Legal Teams