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The New Book Get to Market Now! Available for Pre-Order Today

FOR IMMEDIATE RELEASE

Williamsburg, Virginia:  February 18, 2010

FDA compliance guru, John Avellanet, shows biopharmaceutical and device executives how to speed time to market with new medicines and turn regulatory compliance into a competitive business advantage in his new book, Get to Market Now!  Turn FDA Compliance into a Competitive Edge in the Era of Personalized Medicine.

More than 83% of new medicines never make it to market, wasting billions of dollars, decades of research and development, and millions of patients around the world.  Get to Market Now! provides practical strategies to help executives tap into the secrets of new product development and the FDA quality and regulatory compliance structures to match.  The book teaches readers how to take advantage of evolving FDA compliance requirements and cutting-edge new product development techniques to bring new medicines to market faster, easier, for less cost and less risk.

At the heart of the book is a systemic, structured new medicinal product development process – from discovery and preclinical through the postmarket stages – and a blueprint for a regulatory compliance and quality system designed to enhance business flexibility and encourage innovation.

Based on years of work in his own career, plus advising clients around the world, author John Avellanet walks readers through how to:

The book is packed with “to-do” lists and full of links to online resources, templates, checklists, downloads, and other valuable material.

Get to Market Now! will be published May 1, 2010, but is available for pre-order today through Barnes & Noble and other fine booksellers.  Journalists and editors who would like a complimentary review copy need only contact the publisher, Logos Press (www.logos-press.com).

Mr. Avellanet has gained tremendous acclaim on his speeches, workshops and teleconferences for corporate clients and conference venues around the world.  Enthusiastic testimonials from attendees cover his speaking page on his website.  Conference organizers and program directors repeatedly note that he gets the highest evaluations of any of their speakers.

John Avellanet is the author of more than 100 articles, is the FDA compliance columnist for several international industry journals, and is the founder of the private compliance advisory firm, Cerulean Associates LLC.  Every month, he publishes the regulatory intelligence and quality systems advice newsletter, SmarterCompliance™.  Learn more about Mr. Avellanet on his blog, http://www.ComplianceZen.com.  To engage his private consulting services for FDA-regulated firms, contact him through his company’s website:  http://www.ceruleanllc.com

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