Porzio Life Sciences’ Kiaema Reid, Senior Regulatory Analyst, is a contributor to the composition of the “Pharmaceutical and Medical Device Compliance Manual,” a joint project of the Center for Health & Pharmaceutical Law & Policy at Seton Hall University School of Law, the Food and Drug Law Institute, and the American Health Lawyers Association. Reid discuss the Federal and State Aggregate Spend and Marketing Disclosure Laws. Within this scope, she focuses on the regulatory landscape and the evolution of transparency and their effects on the interactions between life sciences companies and health care practitioners, health care organizations, and teaching hospitals
The “Pharmaceutical and Medical Device Compliance Manual” is a comprehensive manual providing helpful tools and guidance for health and life sciences attorneys, compliance officers, and other members in the pharmaceutical and medical device industries.
For more information on the Manual, or to purchase a copy, please click here.