After seven years, FJC Tea and Spice company continues to value their investment in InstantGMP’s all-in-one solutions Capturing Manufacturing, inventory, and quality data.
CARY, N.C. –
As the innovators of the all-in-one system to capture manufacturing, inventory, and quality data, InstantGMP™ is always developing new features for our software to improve user experience, enhancing existing modules, and providing new manufacturing solutions that adhere to the latest industry trends and regulations. For more than seven years, FJC Tea and Spice, a leading supplier to some of the industry’s top contract manufacturing organizations, has benefitted from the new features included in every release of InstantGMP™ PRO.
FJC Tea and Spice now enjoys an array of new InstantGMP™ PRO manufacturing solutions functionalities.
With our latest release of InstantGMP™ PRO software, FJC Tea and Spice now enjoys an array of new functionalities that help simplify their processes, enhance the security of their internal documentation, and reinforce good manufacturing practices (GMP). InstantGMP™ PRO’s new data encryption and security measures not only provide FJC Tea and Spice with cybersecurity built into the system but also allows them to determine which internal documents they upload to the system have protected access. Once these designated documents are uploaded to the system, the information contained in them is encrypted. These documents are only accessible to authorized users who have an encryption key that allows them to read vital information.
In addition to built-in cybersecurity and the option to secure any documentation stored in the system, FJC Tea and Spice also benefit from the software’s newly upgraded requisition modules that improve the visibility of individual purchase orders generated by the software. This enhanced visibility improves the requisition process when new orders are submitted to a third-party vendor.
While these new enhancements are incredibly rewarding, the latest release feature that FJC Tea and Spice find most beneficial is the ability to add a predecessor rule to the electronic batch record system. With this new feature, they lock in defined steps to a specific batch record and ensure that the operator completes all steps before moving to the next step.
Their experience with the solution
“To say that we’re impressed by each new release of InstantGMP™ PRO software is an understatement. With the new predecessor rule feature, we’re not only able to define the steps required to manufacture a batch, but we can stop an operator from skipping a step of the production process,” said John Cantafio, owner of FJC Tea and Spice. “The system continues to provide us with greater control over our manufacturing, reduce the risk of operator error, and ensure that our processes adhere to GMP standards.”
“Thanks to the feedback we receive from long-standing clients like FJC Tea and Spice, we gain new insight into the many challenges manufacturers and suppliers face every day,” said Dr. Richard Soltero, President of InstantGMP. “With this information at top of mind, we can assess our system to develop new features that solve pain points and include enhancements in our future releases. This makes our product appealing to new audiences and more rewarding for existing clients.”
If you’re interested in learning more about the latest release of InstantGMP™ PRO software and the many solutions it provides for manufacturing, inventory and quality control, please contact our team today.
About InstantGMP
Founded by pharmaceutical industry veteran Dr. Richard Soltero, InstantGMP, Inc., offers affordable all-in-one manufacturing, inventory and quality software. The company develops cloud-based electronic batch record software and standard operating procedures specific to industries that are required to follow FDA manufacturing regulations and Good Manufacturing Practices (“GMP”).
As a manufacturing software company, InstantGMP™ pioneered accessible, easy-to-use electronic batch record software for products manufactured using GMPs. The software simplifies quality processes, streamlining documentation, approval procedures, and organization of quality documentation in electronic format. It also provides quality checks, workflow processes, and facilitates compliance with FDA requirements.