Vitamin Lawyer Vital Connection University Webinar

VITAMIN CONSULTANCY UPDATE eMEMO

"Alternative Medicine" or Advanced Health Care?
A Vitamin Lawyer Webinar

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Memorandum from Ralph Fucetola JD

January 21, 2014

To: Vitamin Consultancy Contact List:

I am hosting a live online webinar this Saturday morning at Vital Connections University. Yes, it will be archived.

You can sign up here. You should just do it; get yourself ready for the coming year!

http://www.vitalconnectionuniversity.com/course/category.php?id=4

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Natural Solutions Tenth Anniversary Retrospective Video
Featuring General Bert, Doctor Rima and Counsel Ralph
http://youtu.be/dtWoKqrb8eY

AER Reporting Portal: New from the FDA

VITAMIN LAWYER UPDATE eMEMO

Natural Solutions Tenth Anniversary Retrospective Video
Featuring General Bert, Doctor Rima and Counsel Ralph
http://youtu.be/dtWoKqrb8eY  

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Memorandum from Ralph Fucetola JD FDA Unveils New Website January 16, 2014 To: Vitamin Lawyer Contact List Latest "shot across the bow" from the FDA: it will now be easier than ever before to report dietary supplement "adverse reactions." You may remember last year when certain Congressional critics of dietary supplements were surprised at the very low numbers of "adverse reactions" being reported for dietary supplements, as compared to, for example, drugs. This couldn't be due to the relative safety of dietary supplements, could it? Of course it could be! It must be a "reporting problem" to be corrected by more bureaucracy... Natural Products Insider reports: "Distributors, manufacturers and packers of dietary supplements now can submit AERs (adverse event reports) through an electronic filing system, FDA announced Monday. Companies can submit the AERs through the Safety Reporting Portal ..." The portal is here: https://www.safetyreporting.hhs.gov/fpsr/WorkflowLoginIO.aspx?metinstance=0AA55778888D1638B9111B3C7655A47D82FD5D6F If you have your own dietary supplement label, you need to be aware of the increased level of regulation you need to prepare for in  2014: http://vitaminlawyerhealthfreedom.blogspot.com/2013/07/fdatargeting-vitamin-companies.html You really and truly understand that this is the year when you must get your paperwork in order! That means having meaningful Standard Operating Procedures for your company or practice. In means being in a "state of control" with your manufacturer, shipper and other service providers. AND BEING ABLE TO PROVE THAT TO THE INEVITABLE FDA INSPECTION!  In short, you need the Vitamin Lawyer SOP/GMP Training Program! www.VitaminIndustryCompliance.com #914.966.8053 - SOPclienthelp@gmail.com

Memorandum of January 9, 2014: Virtual Audits

VITAMIN LAWYER UPDATE eMEMO

SPECIAL TO MY LIST: BOB CONNOLLY'S HEART RATE VARIABILITY TRAINING!
Special Offer Has Been Extended!

Memorandum from Ralph Fucetola JD January 9, 2014 To: Vitamin Lawyer Contact List Looking forward to a prosperous new year! Three important ideas for your new year! And, next issue of the eMemo, look for my exciting new Webinar to be provided through Vital Connection University Online -- January 25, 2014. [FIRST] The Advanced Health Care practitioners on this list should be very interested in an educational program Robert E. Connolly, D.Sc., L.Ac. has made available especially for the Vitamin Lawyer eList. I've known Bob for decades and can personally attest to his skill as an Advanced Health Care Practitioner. He has become quite the expert in Heart Rate Variability and wants to share what he knows about this FDA-permitted evaluation system.  NOW, and until the end of business Monday, December 30th, you can receive his amazing training FREE (I promise you, this is worth thousands!) when you buy the HRV device for a special low price... and time payments are available. I've reviewed Bob's training materials. They are more than good. And the device is... spectacular! "HRV Measures The Difference Between Expenditure or Discharge of Energy, and the Regeneration or Consolidation of Energy." -- Bob Connolly More here: http://us6.campaign-archive1.com/?u=f28a9391e1093e6a00ed0734f&id=99bbd3f2e6&e=06c7e90f5d IF YOU WANT TO LEARN, CALL SHER KOMISAR RIGHT NOW! #914.966.8053 - SOPclienthelp@gmail.com [SECOND] SPECIAL INTRODUCTORY OFFER! FDA expects label-owners and manufacturers to have third-party compliance audits on a regular basis. Following a standard twenty page, 190+ item check list, we take a virtual tour of your contract manufacturer facility (using Skype or similar) to provide my third-party FDA eGMP compliance audit.  The audit tour is recorded and the Audit Report includes extensive review of all GMP requirements together with still images from the tour, confirming compliance. Contact me for pricing and reservation of time. The average audit takes 6 hours of my time; about an hour of your time. Reserve your Virtual Audit now; you should contact my Certification Program Coordinator, Sher Komisr here: #914.966.8053 - SOPclienthelp@gmail.com [THIRD] You really and truly understand that this is the year when you must get your paperwork in order! That means having meaningful Standard Operating Procedures for your company or practice. In means being in a "state of control" with your manufacturer, shipper and other service providers.  AND BEING ABLE TO PROVE THAT TO THE INEVITABLE FDA INSPECTION!  In short, you need the Vitamin Lawyer SOP/GMP Training Program! www.VitaminIndustryCompliance.com #914.966.8053 - SOPclienthelp@gmail.com