Porzio Life Sciences provides Aggregate Spend Regulatory Compliance software solutions for Pharmaceutical, Medical Device & Biotech companies comply with Affordable Care Act and Sunshine Act.
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Elizabeth Kim and Kiaema Reid, Contributing Authors of the Pharmaceutical and Medical Device Compliance Manual


October 11, 2012

 

Porzio Life Sciences’s Elizabeth H. Kim, Manager of Regulatory and Compliance Services and Kiaema Reid, Senior Regulatory Analyst, are contributors 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.  Kim and Reid discuss the Federal and State Aggregate Spend and Marketing Disclosure Laws. Within this scope, they focus 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.

 


 

 

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