Supplement Maker Warned by FDA for Misbranding and Procedural Violations

Per FDA News, Sanapac, a dietary supplement manufacturer, was notified by the Food and Drug Administration for GMP violations, adulterated products, and misbranding products after an inspection in 2016. After an inspection in November, FDA inspectors returned the following month and found numerous issues in regards to the lack of written Standard Operating Procedures for[…]

FDA Prioritizing GMP Re-Inspections for High-Risk Dietary Supplement Firms

This article was sparked from reading Josh Long’s post on Insider Law about inspections of Dietary Supplement firms for compliance with Good Manufacturing Practices (GMPs). These firms had previously failed an inspection and were targeted by the FDA as “high-risk”, thus precipitating the need for re-inspection. Josh reports that half of the dietary supplement companies[…]

InstantGMP MES v2.052 Materials & Projects

In the newest version, InstantGMP MES v2.052, we’ve added a multitude of new features and updated existing ones to make them more efficient for users. New Client Features The Client menu is now under the Administration module and no longer on the Projects sub-menu. This allows for a user to input their client information much earlier[…]

InstantGMP MES v2.052 Released

Cary, NC – InstantGMP, Inc. announces the release of InstantGMP MES v2.052 with amazing new features InstantGMP, Inc. added many great new functions and updates to their electronic batch records software to enhance their user’s experience. “We are excited about the new master production record and batch production record features in our v2.052 release” said[…]

InstantGMP MES v2.052.000

Let’s take a look at what’s new in the newest release, InstantGMP MES v2.052.000! New Functionalities Expanded badge signature capabilities to system-wide usage. Added new workflows focused on Project Management functionalities allowing for projects to include multiple products for multiple clients with multiple user access control under multiple roles. Added new Material Classifications to help employ[…]

The GMP Compliance Conundrum

The acting deputy director of the Division of Dietary Supplement Programs at the FDA, Cara Welch, Ph.D., left the author of this article with some confusing takeaways: If you are a Dietary Supplements manufacturer who wants to learn good manufacturing practices, read the GMPs for dietary supplements and apply them, otherwise, you are at risk of[…]

Natural Products Insider interviews InstantGMP’s Robert Pochadt

Natural Products Insider interviewed Robert Pochadt, Director of Sales at InstantGMP, Inc. to find out more about how we help customers manage FDA mandated documentation with SOPs and Electronic Batch Record Software so they can go paperless and “ditch the clipboard” Check out Robert’s Interview! Related Posts:FAQFDA Prioritizing GMP Re-Inspections for High-Risk Dietary…FDA to CBD:[…]

InstantGMP and Muscadine Products Corporation

Muscadine Products Corporation (MPC) manufactures a variety of muscadine-derived products including powders, juices and jellies. Their paper system for organizing manufacturing records was difficult to manage and had a tendency to get messy being in a facility that produced juices. MPC began using InstantGMP MES in October, 2014. With all of their records contained in[…]

Specifications Celebration

It’s Specifications celebration time! As you can see, the InstantGMP team is VERY excited about our improved Specifications module! Related Posts:FAQSoftware ModulesContact UsComing in 2015 – Barcodes, BIN Location and Improved…Standard Operating ProceduresDemo

Specification Improvements Explained

The latest version of InstantGMP MES includes improvements to the Specifications module. These improvements include filtering options and the ability to view all pertinent information on one page. Our hope is that these changes make your use of the Specifications function easier. Gretchen, our Customer Service Associate and Quality Expert, explains the changes in just[…]