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Requirements for Raw Materials Testing

Another great question for a member of our GMP for Dietary Supplements group: Are there any specified requirements for raw materials testing? There are specific requirements to release raw materials which are based on the final product in which the…

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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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Air Pressure in a Supplement Manufacturing Facility

A member of our GMP for Dietary Supplements group recently inquired about positive air pressure requirements for dietary supplement manufacturing facilities. The short answer is no, there are no specific requirements and there's no minimum for differentiating pressure (DP) for…

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InstantGMP to Attend Natural Products Expo East

The  InstantGMP team is excited to be attending Natural Products Expo East September 18-20 in Baltimore, MD! This show is expected to be even bigger than previous years and we hope to meet with supplement and specialty food vendors with…

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How to Maintain a Clean Room

A clean room is a heavily controlled environment where regulated products, such as dietary supplements, are manufactured. The purpose of the controlled area is to keep contaminants to a minimum in order to create high-quality products. Sources of contamination include:…

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Quality and SOPs in E-Liquid Manufacturing

Quality is a term typically used in the e-cigarette industry to describe flavor.  When it comes to manufacturing, it is something else entirely.  Quality is defined as meeting specifications.  This means that each time a product is made, it meets…

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Message from an InstantGMP User

We love to hear success stories from our customers! Here is a message from an InstantGMP User who especially values the Quality initiatives the software provides: Hello! I hope all is well with you. I see that you continue moving…

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Quality by Design – Implementation and Challenges

The pharmaceutical industry has implemented regulatory practices such as Process Analytical Technology (PAT), Good Manufacturing Practices (GMP), and now Quality by Design (QbD) to make sure that consumers get only quality and safe pharmaceutical products. The FDA defines QbD as…

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