InstantGMP™ VAPE

FDA Tobacco Deeming Regulations | E-Liquid Manufacturing Software InstantGMP™ Vape
 

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.

Be sure to read this case study to learn about how InstantGMP™ Vape can transform your operation: InstantGMP™ Customer Case Study (Docx format)

FDA Tobacco Deeming Regulations | E-Liquid Manufacturing Software InstantGMP™ Vape

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