InstantGMP™ Release Notes version 3.004.001

New Functionalities Materials and inventory can now be imported from a spreadsheet that is downloadable from the application. This new functionality allows users to easily transition their inventory information from legacy systems to the InstantGMP™ Inventory Management solution. The solution includes import of: Materials Specification version placeholders with automatic signatures that reference paper specs OR[…]

InstantGMP, Inc. Announces Unprecedented Game Changing Feature to Electronic Batch Record Software

Cary, NC: June 26, 2017.  InstantGMP, Inc. announces a remarkable technological advancement to its batch management software, InstantGMP™. InstantGMP™, Inc. is the developer of the only affordable cloud based software that manages and organizes the manufacturing of products regulated by the FDA. This release features a transformative new feature called Dynamic Fields that give users[…]

InstantGMP™ Release notes for version 3.002.007 and 3.002.008

We’re working on a major update to InstantGMP™, but in the meantime, we’ve added some new functionalities and improvements! InstantGMP™ Release notes for version 3.002.007                      New Functionalities Creation of outgoing WIP/FG materials now allows for the inclusion of strength and suffix which becomes part of the material name which is, in turn, auto assigned a[…]

US and EU Sign Agreement to Mutually Recognize Drug Manufacturing Inspections

In 1998, the European Union (EU) and the US signed the Mutual Recognition Agreement (MRA) with provisions specifically about current Good Manufacturing Practices (cGMPs) for drugs but were unable to start implementation. Since 2014, both the US and European Medicines Agency (EMA) revived agreement talks concerning the cGMP provisions. Starting in 2012 with the passage[…]

InstantGMP, Inc. and CfPA Present: Electronic Batch Records: Benefits and Implementation Planning Online Training Course

InstantGMP, Inc. and the Center for Professional Advancement (CfPA) have collaborated on a course entitled, “Electronic Batch Records: Benefits and Implementation Planning” InstantGMP, Inc. and CfPA have designed this course with cGMP manufacturing professionals looking to improve or enhance their process, traceability and FDA compliance with electronic batch records in mind. This course invites professionals[…]

E-Vapor Law Symposium – Early Bird Registration Still Available, Save $500

Attention E-Liquid Companies: Are you ready for 2017? Regulation deadlines are fast approaching, but the E-Vapor Law Symposium is here to get you ready. Keller and Heckman are leaders in the FDA legal landscape. They are hosting an E-Vapor Law Symposium in their Washington, D.C. offices on Thursday, February 2 – Friday, February 3, 2017.[…]

3.002.002 Release Notes

3.002.002 is a minor update to the software and includes fixes to the old receipt number error in 3.002.001 and a production number error from 2.048.001. We’re developing some great new features and functionalities for 2017, so stay tuned! Fixes • Display Error – On Version 3.002.001 we introduced new Inventory functionalities, but when you[…]

InstantGMP™ Release notes for version 3.002.001

  Last week we previewed the newest additions to InstantGMP™! In this post, you will find specific information about the new functionalities, improvements, and fixes in our latest version, 3.002.001: New Functionalities When receiving materials, users can create Multiple Receipts from one requisition After receiving materials, users can Split a receipt into Multiple Lots Now[…]