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InstantGMP, Inc. and CfPA Present: Electronic Batch Records: Benefits and Implementation Planning Online Training Course

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[…]

3.002.002 Release Notes

3.002.002 is a minor update to the software and includes fixes to the old receipt number error in 3.002.001 and a production number error from 2.048.001. We’re developing some great new features and functionalities for 2017, so stay tuned! Fixes • Display Error – On Version 3.002.001 we introduced new Inventory functionalities, but when you[…]

InstantGMP™ Release notes for version 3.002.001

  Last week we previewed the newest additions to InstantGMP™! In this post, you will find specific information about the new functionalities, improvements, and fixes in our latest version, 3.002.001: New Functionalities When receiving materials, users can create Multiple Receipts from one requisition After receiving materials, users can Split a receipt into Multiple Lots Now[…]

InstantGMP™ INV, First Affordable Cloud-Based, Validated cGMP Inventory Management Software

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[…]

InstantGMP, Inc. Adds Impressive New Features & Functions in v3.002.001

  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[…]

New Release & New Update Coming Soon!

We’ve been busy here at InstantGMP, Inc. preparing to release a new, awesome product and have added some really helpful functionalities to our software! It’s almost ready, but here’s a sneak peek: Related Posts:FAQInventory ManagementSOFTWARE LICENSE AGREEMENTMaster Production RecordLicense Agreement Terms (Old)Barcode Scanning Capability

InstantGMP™ Transforms Manufacturing with Equipment Integration

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[…]

FDA Releases Unique Device Identifier Draft Guidance

Zachary Brennan of the Regulatory Affairs Professional Society (RAPS) outlined the guidance from the Food and Drug Administration (FDA) about the expected content and forms for the Unique Device Identifier (UDI) for medical device manufacturers and distributors that are coming into effect. UDI Background A UDI is composed of: A device identifier One or more[…]