skip to Main Content

InstantGMP Enters New Territory With Latest Client

With the addition of Torigen Pharmaceuticals to its client base, InstantGMP now provides software solutions for the veterinary biologics industry. CARY, N.C. November 15, 2022 -  InstantGMPTM, creators of the all-in-one manufacturing and quality system, breaks new ground with the…

Read more
Two operators at a pharmaceutical manufacturing facility using InstantGMP PRO’s MES software to ensure accuracy during the production process.

Understanding The Difference Between ERP and MES Software

When searching for software solutions for manufacturing facilities, two acronyms often appear automatically: ERP and MES. While there is a lot of information online about these two software systems, many of the articles consider these two solutions interchangeable.  Unfortunately, that’s…

Read more
A life sciences executive in their office watches a demonstration of MES software on a laptop while speaking on the phone with an InstantGMP sales representative.

A Guide To MES Software For Life Sciences Executives

The responsibilities of life sciences manufacturing executives are diverse.  Besides overseeing the business and administrative needs, executives are also tasked with finding new ways to lower costs, improve productivity, introduce new policies and processes,  and ensure stakeholders and regulatory agencies…

Read more

InstantGMP Celebrates Four Years With Cartesian Therapeutics

InstantGMP PRO software allows the renowned RNA cell therapy company to move from preclinical development to clinical testing more efficiently and effectively! CARY, N.C. August 16, 2022 -  InstantGMP™ celebrates four years of proudly supporting  Cartesian Therapeutics’ groundbreaking work in…

Read more
Technician running a software validation process for a manufacturing client.

Keys to Success For GMP Software Validation

Before a GMP manufacturing facility implements a software system into their operations, that system must go through a comprehensive software validation process.  This multi-part process ensures that a manufacturing facility’s software is compliant with all FDA regulations, and all Good…

Read more
Back To Top