Supplement manufacturing facilities following Good Manufacturing Practices are expected to set, meet and document specifications for all incoming and outgoing materials. Failure to do so could lead to a regulatory action such as an injunction. GMP Specifications are needed for:…
Managing inventory in a way that is compliant with GMP can be challenging. Regulatory measures specific to handling inventory are included in the Dietary Supplement Health and Education Act (DSHEA). The regulations apply to all incoming materials, work-in-progress materials, and…
InstantGMP MES controls all material specifications attributes by automatically assigning part numbers. Only approved materials can be used in Batch Production Records. Here are a few frequently asked questions about the material specifications component of the software: Can I import Materials…
We were thrilled to meet so many new people and learn about new products at Natural Products Expo East! Our mission? To learn how InstantGMP MES can better serve the supplement and natural product industry. Automation of GMP was a…
After recording an updated demo, I was reminded of all of the benefits InstantGMP MES awards its users. It is the only cloud-based manufacturing software that guides users through a GMP workflow. It offers tools to manufacturers that that provide…
Batch Production Records (BPR) document the when, how, by whom with what tools and what environment a product was produced. The FDA required Batch Production Records for every batch created in a manufacturing facility. InstantGMP software allows you track batches…
Cloud software is likely part of your every day life. Gmail, Yahoo Mail, Google Drive, Facebook and Netflix are all examples of cloud software. The term refers to programs that are accessed via the internet rather than a program installed…
Understanding GMP for inventory can be challenging for a growing supplement manufacturing company. InstantGMP is here to make GMP compliance easy for growing dietary supplement businesses while also providing you with accurate information on current Good Manufacturing Practices. How does…
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…
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,…