Porzio Life Sciences, LLC
In 2004, Porzio formed its first wholly owned subsidiary, Porzio Life Sciences, LLC, to help Life Sciences companies comply with state marketing and sales laws and regulations. Since that time, Porzio Life Sciences has provided regulatory and consulting services to more than 80 members of the Life Sciences industry. Porzio Life Sciences offers a portfolio of compliance products and services that assist pharmaceutical, biotech and medical device companies with state law monitoring, licensing, distribution and state reporting efforts.
One of Porzio Life Sciences’ innovative products, the Porzio Compliance Digest (“PCD”), is the premier database for tracking state laws, regulations and pending legislation in all areas impacting pharmaceutical marketing and sales compliance. Porzio Life Sciences personnel continuously monitor the legal landscape and incorporate relevant legislative changes and developments into PCD. PCD is the only Life Sciences marketing and sales compliance system that is quality controlled by attorneys. It is also the only state law monitoring system built and maintained by a subsidiary of a nationally recognized law firm that specializes in Life Sciences marketing and sales compliance, as well as pharmaceutical product liability law.
Other popular Porzio Life Sciences products include a series of Compliance Modules (“PCMs”) that provide at-a-glance information on state-specific laws and regulations. The PCMs cover Legend Drug and Controlled Substance Sampling, Wholesale and Manufacturer Distribution, State Disclosures and Limitations and Pedigree Requirements. A Mid-level Practitioner Sampling Authority module addresses sampling of legend and controlled substances by 12 distinct classifications of practitioners. ePorzio enables companies to train and certify personnel on a range of field-force-specific activities.
Porzio Life Sciences, together with Porzio, provides the Life Sciences industry with a full array of consultative and legal services, including sales and marketing practice audits and risk evaluation assessments, promotional material review, contract negotiation, standard operating procedure preparation, and training sessions for Life Sciences industry personnel on legal requirements.
