InstantGMP Attending World Vapor Expo in Miami

The InstantGMP Vape team heads to Miami May 29-31 for the World Vapor Expo! We are looking forwarded to talking to industry leaders about FDA regulations and sharing tips with e-liquid creators on how to follow Good Manufacturing Practices. Speakers that we are looking forward to seeing include Marc Brucker of Sensory Solution and Industry[…]

Indiana’s HB 1432 Imposes Manufacturing Guidelines for E-liquids

If Indiana’s governor signs House Bill 1432 (HB 1432) into law, e-liquid creators would be subject to new manufacturing, label and ingredient guidelines. Manufacturing All mixing, bottling, and packaging activities must take place in a clean room. The manufacturer must be willing to submit to random audits of the facility and the product itself. The[…]

Prioritize GMP Compliance When Choosing Software

This post was written by Robert Pochadt, InstantGMP Sales Director. It is imperative that when considering material management and manufacturing automation software that one evaluates the quality of the regulation checks and balances integral to the system and aims to prioritize GMP compliance. One of the “10 things that ERP and manufacturing systems vendors won’t[…]

Commit to Paperless Manufacturing on Earth Day

Celebrate Earth Day 2015 by committing to switch to paperless manufacturing! In addition to saving trees, paperless manufacturing saves your supplement manufacturing facility time and money. How InstantGMP Helps InstantGMP’s manufacturing software is cloud-based, which means it’s not installed on your computer. it is accessed via the web from a secure link. This means it[…]

InstantGMP Announces Partnership with Marian Boardley Consulting, LLC

We are excited to have the opportunity to team up with regulatory expert Marian Boardley to offer joint services! Marian Boardley specializes in managing compliance projects for dietary supplement manufacturers. Her specialized consulting services complement our electronic batch record software and SOPs nicely. Our hope is that the combination of software and regulatory expertise will[…]

Webinar Preview: Capturing Processes for MBRs

Webinar Preview: Capturing Processes for MBRs On Tuesday, April 21st, InstantGMP and dietary supplement regulatory expert Marian Boardley present Tips for GMP Compliant Master Batch Records. There’s still time to sign up! We will be sharing common issues with Master Batch Records that lead for 483s and how you can avoid them.   MBRs are[…]

E-Liquid Law: Arkansas Manufacture and Sale of Vape Liquid

Arkansas pushes the envelope with E-Liquid Law. Arkansas Senate Bill 978 has been officially approved by both houses and is on its way to the governor’s desk. If signed into law, e-liquid manufacturers and retailers will be e required to have a license issued by the state by May 1st. Additionally, retailers would only be[…]