HEALTH CARE AND LIFE SCIENCES
LEGAL GUIDE TO THE BUSINESS OF MARIJUANA CANNABIS, HEMP AND CBD REGULATION Edgar J. Asebey (Keller Asebey Life Science Law PLLC) and Guilherme Ferrari Faviero (AHF Global Public Health Institute, University of Miami)
This helpful resource for practitioners, cannabis growers, retailers, and other players elucidates upon the regulatory pressures affecting cannabis, hemp, and cannabidiol businesses. This deskbook is authored by a pair of esteemed public health policy practitioners who have worked on varied projects and matters involving Food and Drug Administration compliance and public health matters. Cannabis stakeholders and advisers will find a plethora of case studies, practical insights, and in-depth guidance on the political and public policy issues that impact them and their enterprises on the state and federal levels. Track important cannabis, hemp, and cannabidiol regulatory developments with PLI’s Upkeep Service. 1 softbound volume or digital, 592 pages, $306, Item #396848, ISBN 978-1-4024-4594-1, Updated annually or as needed
HEALTH CARE MERGERS AND ACQUISITIONS ANSWER BOOK
Edited by Andrew L. Bab and Kevin A. Rinker (Debevoise & Plimpton LLP)
Formatted in an approachable, question-and-answer style, this work helps corporate practitioners, in- house counsel, health care lawyers, and health care entity stakeholders understand the legal rights and ramifications of health care-oriented M&A. Readers will receive tips and practices steeped in the experience of several accoladed lawyers with more than 40 years of health care sector M&A experience. Readers will access an informative four-part roadmap through the structuring, due diligence, document drafting, and cross-border considerations health care entities should weigh as they plan and carry out their M&A transactions. Some of the transactions the authors explore include joint ventures, strategic alliances, product and portfolio acquisitions, option transactions, and licensing and collaboration agreements. Keep up with new best practices with PLI’s Upkeep Service. 2 softbound volumes or digital, 1,880 pages, $293, Item #397731, ISBN 978-1-4024-4614-6, Published annually or as needed
MEDICAL DEVICES LAW AND REGULATION ANSWER BOOK Edited by Suzan Onel (Kleinfeld, Kaplan & Becker, LLP) and Karen M. Becker (Precision for Medicine)
This question-and-answer book offers detailed, comprehensive conversations on the pre-market requirements and post-market regulation affecting medical devices and their manufacturers. Readers will find insightful, easy-to-follow discussions from a group of esteemed health care lawyers and professors — all of whom have counseled clients on FDA compliance and enforcement matters. Anyone who counsels or works for a device manufacturer or health care regulatory agency will find instructive discussions of the premarket and post-market requirements and considerations around medical devices, including 3D-printed devices, devices used with regenerative therapies, combination products, restricted devices, custom devices, and radiological products. Keep up with new medical device requirements with PLI’s Upkeep Service.
1 softbound volume or digital, 1,350 pages, $293, Item #397728, ISBN 978-1-4024-4611-5, Published annually or as needed
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