Pharmaceutical Compliance Training
Stay Compliant. Stay Informed.

This course prepares healthcare staff to respond effectively to fire emergencies in medical facilities. Topics include fire prevention strategies, the R.A.C.E. (Rescue, Alarm, Contain, Extinguish/Evacuate) protocol, proper use of fire extinguishers (P.A.S.S. technique), evacuation procedures

This course provides an in-depth understanding of the Foreign Corrupt Practices Act (FCPA), a critical U.S. anti-corruption law that prohibits bribery of foreign officials and mandates accurate financial record-keeping. The course covers legal requirements, enforcement trends, compliance strategies, and real-world case studies to help professionals navigate FCPA risks

This course provides a comprehensive introduction to the General Data Protection Regulation (GDPR), equipping participants with the knowledge to navigate its strict privacy requirements and promote ethical data handling practices

This essential training provides a clear understanding of HIPAA Privacy Rule requirements, helping healthcare industry professionals and organizations protect Protected Health Information (PHI) while maintaining compliance.

This essential training provides healthcare industry professionals and organizations with a clear understanding of the HIPAA Security Rule and its critical role in protecting electronic protected health information (ePHI). Participants will learn to identify security requirements, implement safeguards, and avoid costly violations.

This course provides an in-depth exploration of the U.S. government framework and the evolution of pharmaceutical regulations from early oversight to the modern FDA era. Participants will examine key legislative milestones, regulatory shifts, and the FDA’s expanding role in public health and safety.

This course provides a comprehensive understanding of the HITECH Act and its critical enhancements to HIPAA regulations. Participants will learn how to implement strengthened privacy/security requirements, manage business associate relationships, and comply with modernized breach notification rules in our digital healthcare environment.

This course provides a comprehensive look at the pharmaceutical drug creation process, the FDA’s regulatory role, and the structure of the pharmaceutical industry. Participants will gain insights into how drugs are developed, approved, and brought to market, as well as the key players and organizational frameworks that define the industry.

This critical course equips Medical Science Liaisons (MSLs) and their managers with a clear understanding of the legal and regulatory framework governing field medical activities. Participants will learn to differentiate compliant scientific exchange from promotional activities while operating within FDA, FD&C Act, and industry guidelines.

This course outlines FDA requirements for reporting adverse events involving medical devices under 21 CFR Part 803. Attendees will learn how to identify reportable incidents, complete FDA Form 3500A, and comply with timelines for mandatory reporting. The training is critical for quality assurance personnel, risk managers, and biomedical engineers.

This training provides an overview of The Joint Commission’s National Patient Safety Goals (NPSG), which are designed to improve patient care and reduce risks in healthcare settings. Participants will learn key objectives such as proper patient identification, effective communication among staff, infection control protocols, medication safety, and fall prevention strategies. The course emphasizes compliance with regulatory standards and best practices to enhance patient outcomes.

This training covers best practices for maintaining safety and efficiency in the operating room. Topics include surgical attire, sterile field maintenance, time-out procedures (Universal Protocol), equipment handling, team communication (SBAR), and emergency protocols. Designed for surgeons, nurses, anesthesiologists, and OR technicians.