Update on Proposed FDA Regulations for E-cigarettes

Much to relief of the e-cigarette industry, the comment period for the proposed FDA regulations deeming e-cigarettes as tobacco products has been extended to August 8th. The reason for this the fact that they’ve received a lot of input from the industry and want to hear more. CASAA, the Consumer Advocates for Smoke-Free Alternatives Association,[…]

FAQ Friday: E-signatures and 21 CFR Part 11 Compliance

In 2007, the FDA set forth rules governing e-signatures documentation known as 21 CFR Part 11. This is an important function in Good Manufacturing Practices. Here are a few frequently asked questions about how InstantGMP MES helps your comply with 21 CFR Part 11: Why do packagers, labelers and holding companies have to have Master[…]

InstantGMP President Dr. Rick Soltero Joins AEMSA as Subject Matter Expert

Cary, NC – AEMSA continues to demonstrate the viability and practicality of the Reasonable, Realistic and Sustainable approach to consumer protections and good product stewardship for E-liquid production. AEMSA manufacturing standards remain the only verified self-regulation and practices in the industry (globally).  The FDA’s proposed deeming rules now make the need for comprehensive Industry Specific[…]

Update to InstantGMP Vape Includes Reports, Attachments and More

The newly updated InstantGMP Vape includes even more features to give vape manufacturers’ e-liquid a high-tech edge! In addition to providing documentation and GMP processes, the first manufacturing software designed specifically for the vape industry now includes reports for inventory, equipment calibration and lot traceability. Another new feature is the ability to add attachments such[…]

InstantGMP Vape Update to Include a Report Generator, New Attachments and Other Improvements

InstantGMP, Inc. announces the latest version of InstantGMP Vape, its Manufacturing Execution Software for e-liquids, which will include reports, attachments, improved unit functionality and an import service for new customers. InstantGMP Vape will now include six standard reports – Current Inventory, Equipment Calibration, Stock in Quarantine, Low Inventory, Product Lot Traceability and Vendor Lot Traceability.[…]

InstantGMP MES Update Coming Soon with Reports, Attachments and Other Improvements

InstantGMP MES Update: v 2.045 will be available on July 1st! This update includes many customer requested features such as a report generator and attachments. Here’s an overview of the new features: Report Generator Six standard reports will be included: Current Inventory Equipment Calibration Stock in Quarantine Low Inventory Product Lot Traceability Vendor Lot Traceability[…]

Language of InstantGMP Software

Let’s take a look at the language of the InstantGMP software. You see them on our website, in our training materials and in the software itself – the manufacturing world uses a lot of abbreviations! We’ve defined a few of them for you here:   21 CFR Part 11 FDA regulations covering security electronic signatures[…]

InstantGMP MES v2.045 to Include a Report Generator, New Attachments and Other Improvements

Cary, NC – InstantGMP, Inc. announces the latest version of InstantGMP MES v2.045, its Manufacturing Execution Software, which will include reports, attachments, improved unit functionality and an import service for new customers. InstantGMP MES v2.045 will include six standard reports – Current Inventory, Equipment Calibration, Stock in Quarantine, Low Inventory, Product Lot Traceability and Vendor[…]

E-Signatures and more in our new FAQ section

Do you have questions about E-Signatures and other topics? Get answers to your questions faster and more efficiently with InstantGMP’s expanded FAQ section! We added more questions in all categories including: Master Batch Records and Batch Production Records Why do packagers, labelers and holding companies have to have MBRs and BPRs from the manufacturer? Where[…]

InstantGMP MES v2.045 Release Information Now Available

InstantGMP MES v2.045 release notes are here! The new version includes streamlined workflows, added features, improved user interface and traceability, as well as fixes. New Functionality Material Data Import for large entries of new part #s 6 on-demand Reports: Vendor lot # traceability Batch Production # traceability Low inventory Levels Stock in Quarantine Current inventory[…]