FAQ Friday: Using InstantGMP Software on a Mobile Device

InstantGMP software is cloud-based, which means that you do not need to install anything on your computer – just a web browser, specifically, Mozilla Firefox. Cloud-based software gives users flexibility on the the type of device used in their facility. InstantGMP can run on desktops, laptops or even mobile devices such as tablets. Which mobile[…]

FAQ Friday: Inventory Control for GMP Manufacturers

InstantGMP software includes inventory control tools such as supplier information, specifications, receiving and distribution. Here are a few frequently asked questions about the inventory functions we offer: Where can I enter our own part numbers for raw materials? We do not want to rely on automated numbering in IGMP. There is a field for “Material[…]

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 into InstantGMP? Materials can be imported into InstantGMP MES or InstantGMP Vape. This is done[…]

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 electronically and we are asked many questions about BPR: Can I sign for someone else[…]

FAQ Friday: NEW Knowledgebase for InstantGMP FAQ

InstantGMP FAQ Whether you are just getting started with InstantGMP software or a seasoned user that has a question, InstantGMP’s new Knowledgebase has all the info you need. In addition to common questions about logging in and security features, we also have helpful articles on getting started with GMP compliance  and more in-depth IT-related issues.[…]

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 21 CFR Part 11: Why do packagers, labelers and holding companies have to have Master[…]

E-Signatures and more in our new FAQ section

Do you have questions about E-Signatures and other topics? Get answers to your questions faster and more efficiently with InstantGMP’s expanded FAQ section! We added more questions in all categories including: Master Batch Records and Batch Production Records Why do packagers, labelers and holding companies have to have MBRs and BPRs from the manufacturer? Where[…]

FAQ Friday: Security Within InstantGMP Software

Keeping sensitive data secure is a top priority. All InstantGMP software has built in security functions. Security can be configured for each screen by an administrator and access to sensitive data is prevented. Since InstantGMP is cloud-based software, we receive many questions about security: How is the data center physically secured? The data center where[…]