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Good Supplement Manufacturing Practices: GMP Specifications

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:…

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Inventory Control Series Part 1: Suppliers and Specifications

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…

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FAQ Friday: Material Specifications

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…

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Our Day at Natural Products Expo East

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…

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FAQ Friday: Batch Production Records

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…

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What is GMP for Dietary Supplement Inventory Control?

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…

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FAQ Friday: E-signatures and 21 CFR Part 11 Compliance

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…

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Update to InstantGMP Vape Includes Reports, Attachments and More

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,…

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