With the release of the FDA's deeming regulations, the E-Liquid and vape product market changed. Our deeming regulations software, InstantGMP™ Vape is an all-in-one batch and quality management solution ideal for manufacturers of E-Liquids for electronic cigarettes looking to better manage inventory, add complete traceability become cGMP, or comply with new regulations for tobacco products. With InstantGMP™ Vape, there are a multitude of benefits that can save your company in labor and production costs by automating and streamlining your workflows. Want to keep all your documents in one place or have a dedicated quality management system? Check out the quality assurance and document management modules.
Here are some of the ways that InstantGMP™ Vape can help you:
- Introduces FDA regulatory concepts such as Master Production Records and Batch Production Records
- Improves the quality and consistency of your E-Liquids
- Electronically keeps track of all of your batches
- Establishes traceability in the event of a customer complaint and minimizes risks of recall
- Reduces the complexity of manufacturing batches
- Copies existing recipes or make adjustments with ease
- Updates inventory levels in real time
- Scales batches with the click of a button for quick response to customer orders
- Recalculates material quantities automatically on Bill of Materials and in manufacturing instructions
InstantGMP™ VAPE Features
Have questions? Want to talk to a live human being?
Hi, I’m Robert Pochadt, Director of Sales at InstantGMP, Inc. I’d love to show you how our track and trace manufacturing software can help you improve productivity.
You can request a demo by completing the form on this page or give me a call at (215) 968-5414.