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InstantGMP, Inc. and the Center for Professional Advancement (CfPA) have collaborated on a course entitled, “Electronic Batch Records: Benefits and Implementation Planning” InstantGMP, Inc. and CfPA have designed this course with cGMP manufacturing professionals looking to improve or enhance their process, traceability and FDA compliance with electronic batch records in mind. This course invites professionals[…]
Cary, NC – InstantGMP, Inc. is announcing the release of InstantGMP™ INV, the first affordable cloud-based, fully validated cGMP inventory management software system for manufacturers regulated by the Food and Drug Administration (FDA) that also complies with 21 CFR Part 11. InstantGMP™ INV fulfills a need for manufacturers within the FDA regulatory sphere that must[…]
Cary, NC – InstantGMP, Inc. announces a new update to their Electronic Batch Record software, InstantGMP™ v3.002.001. New features and functionalities have been added after listening to feedback from users. These new features and functionalities take the software to a new level and makes manufacturing with Good Manufacturing Practices (GMPs) even simpler. Split Receipts[…]
Note: this article was written by InstantGMP, Inc.’s own, Kelly Waters, for publication in PharmaTimes and is available here. This election cycle, there are two radically different candidates: the magnanimous tycoon Donald Trump representing the Republicans and the experienced former First Lady, former Senator, and former Secretary of State, Hillary Clinton representing the Democrats. After[…]
If you haven’t already registered, time is running out! Our webinar is tomorrow, Tuesday October 4th 2pm EST! Register now. Related Posts:Batch Production RecordFAQSoftware FeaturesContact UsSolutionsAdministration Module
The quality experts of InstantGMP, Inc. will be holding a webinar about changing from paper-based systems to electronic manufacturing for FDA regulated products. Registration is free until 10/1 by using the code earlybird! Take a look at our special preview video. Why You Should Attend Learn about how paper cause inefficiencies, errors, cross-departmental miscommunications,[…]
Click here to register. Register before 10/1/2016 and use the code earlybird to attend for free! Related Posts:InstantGMP, Inc. Announces Webinar: Changing from…DemoGMP Compliance CostWebinar: Federal, State and Self-Regulation of E-cigarettesWhite PapersNew Approach for a New Start-Up: Innovative Formulations…
Cary, NC – The Quality and Manufacturing experts from InstantGMP, Inc. will be conducting a webinar on October 4th, 2016 entitled “Changing from Paper-Based to Electronic Manufacturing of FDA Regulated Products”. Despite all the technology we use to automate our daily lives, manufacturing documentation remains paper-based and can cause many problems from cross-departmental miscommunication, redundancies,[…]
Cary, NC – InstantGMP Inc., creator of an Electronic Batch Record system, InstantGMP™ MES 3.0, announces the release of a new feature that connects equipment on the production floor with its cloud-based software. The feature is aimed at helping companies that use InstantGMP™ MES to take their compliance and quality to new levels by accurately[…]