Our New PMTA Pre-Plan!
Have you heard about our Pre-Plan? If not explore more here!
North Guide Blog Solutions
From the Newest in FDA Announcements and the Hottest Legislation to Handy Tips and Tricks for those in Business read our exciting Blogs!
CBD Consultations
We have officially opened our CBD Consultations to the public, when CBD is flooding the market now more than ever its good to have an experienced team on your side to make sure your products won’t be pulled from the shelves.
About Us
Here at North Guide we are more than consultants we are Experts in Data Management and GMP Creation. We design, create, and master entire systems for clients that encompass all aspects of the business. We have kept our clients ahead of the curve that way new legislation and regulations never slow them down. We make sure our clients FDA accounts and regulations are always up to date and we never let anyone’s accounts or licenses fall behind. Let North Guide Solutions take your company into the future, because you should never head into a new venture without an experienced guide!
North Guide we would be no where without our own northern stars! Meet the faces of our team that have made North Guide the trusted name in the Industry since day one!
Monica Schick
CEO of North Guide Solutions, as well as the creator of the Vapor Quality Summit. Monica has over 10 years in manufacturing, specializing in quality management and regulatory compliance. She has spent most of her time in e-cigarettes, focusing on Good Manufacturing Practices for the e-liquid manufacturers and consulting on regulatory issues. Her specialty is the creation of quality systems and evaluating companies for product stewardship.
George Obispo
George has 10+ years’ experience working in laboratory and GMP settings, consulting for both Fortune 500 and upstart companies in Food, Tobacco, and Cannabis. George specializes in building robust and validated quality management systems in both manufacturing and laboratory settings.
Introducing a new member of the North Guide team our very own Senior Regulatory Attorney!
Joshua Ari Van De Riet
Joshua is a regulatory attorney specializing in FDA law and regulation. Joshua graduated from the University of Baltimore School of Law and earned a graduate certificate in Pharmaceutical and Medical Device Law and Compliance from Seton Hall Law School. Joshua began his career in tobacco law and regulation 10 years ago at the Center for Regulatory Effectiveness and continued his work at the FDA’s Center for Tobacco Products where he served as Lead Regulatory Counsel.