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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. These
reports can be accessed quickly and easily, saving time on the
manufacturing floor. Custom reports will also be available for an
additional cost.

“We have been excited to see that e-liquid manufactures are
very quality conscious” said Rick Soltero, President of InstantGMP, Inc.  “Our newest version of the InstantGMP™ Vape software is going to make their ability to make high quality product even easier.”

In addition to the reports, users will be able to use up to
five labeled attachments to Material Receipts and Status pages. This
feature will enable manufacturing and QA employees instant access to
valuable information such as Certificates of Analyses, MSDS sheets and
test results for specific e-liquid batches. With the FDA turning its
eyes towards the vape industry, having these reports will prove to be
valuable in showing commitment to quality, consistency and GMP.

In this software update, InstantGMP has also made
improvements to unit conversions and streamlined the overall system
process for increased intuitiveness.  The software allows e-liquid manufacturers to have the benefits of documentation without having be IT or GMP experts.

The InstantGMP Vape update will be available on July 1st.
A data import service will be included for all new InstantGMP
customers. Please visit for sales and contact


About InstantGMP Vape

InstantGMP™ Vape is the first manufacturing software system
created specifically for producing e-liquids and juices for vaping
products that are manufactured using Good Manufacturing Practices. All
InstantGMP software systems are developed to meet the standards of cGMP,
GAMP and 21 CFR Part 11.

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