FDA to CBD: You Are Not a Dietary Supplement

Hank Schultz wrote up a piece via Nutra Ingredients USA that the FDA sent out warning letters to eight companies marketing dietary supplements containing CBD. The letters also mention illegal drug claims based on CBD being the active ingredient in two drugs currently in development. What is CBD? Cannabidiol (CBD) is a fraction of the[…]

InstantGMP™ MES v2.052: Information for Prospective Customers

Thanks for joining InstantGMP for our new feature series, we are excited to launch InstantGMP™ MES v2.052 with streamlined workflows, more options and more smart fields! We have incorporated industry expertise, customer feedback and new capabilities in order to make your job as a Quality Manager, Project manager, Production supervisor or operator easier. Specifications toggled off[…]

InstantGMP MES v2.052 Master Production Records

We’ve made a number of changes to the Master Production Records. Here you will find a great primer for everything coming in the latest update.   The status of an MPR is now in the leftmost column and MPRs can now be approved or rejected. There are four statuses: Approved, Locked, in-Progress, and Rejected. Approved:[…]

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[…]

New FDA E-Cigarette Regulations Coming

E-cigarettes will soon be regulated under tobacco products as a rule proposed by the Food & Drug Administration (FDA). The rule is currently being reviewed by the White House Office of Management and Budget’s Office of Information and Regulatory Affairs. It will be several weeks before the proposed rule is formally approved and any action[…]

Booming Natural Supplements Business in China

From Natural Products Insider, health food sales in China are estimated to reach RMB300 billion ($47.5 billion USD) by 2019. More and more Chinese consumers are looking to natural supplements as rates for certain illnesses such as lung cancer and breast cancer are on the rise, and they are looking to purchase foreign health products. It[…]

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:[…]