Cary, NC – InstantGMP, Inc.,
the manufacturing software company that pioneered accessible,
easy-to-use electronic batch record software for products manufactured
using Good Manufacturing Practices (GMP) has just completed development
of a report generator for their Manufacturing Execution System software.
InstantGMP MES is the first cloud based system created specifically for
use in manufacturing FDA regulated products. It will now provide the
benefits of controlled documentation and GMP regulated queries without
any IT overhead or need for regulatory experts.
“We were hit immediately by three key findings when our discussion with
FDA regulated manufacturers began”, says Dr. Richard Soltero, President
and founder of InstantGMP. “They are all extremely passionate about
their product quality. And they’re business people first; they see GMP
as a gold standard that can help them maintain their customer’s loyalty.
Finally, the industry really understands the concept of building
quality into their processes and applies the principals of GMP
throughout.
“With a report generator function now available,” Dr. Soltero continues,
“GMP product makers now have an electronic manufacturing platform that
efficiently automates standard reporting for any number of queries with a
set of per-configured reports that can locate specific lots or batches,
or report stock levels and restock requirements. The system can also be
enhanced with customized reports that individual specific needs.
Manufacturing FDA regulated product using best practices is easy to
achieve with InstantGMP™ MES.”
InstantGMP, Inc. develops web-based
software for manufacturing products that must comply with current Good
Manufacturing Practices (cGMP) and FDA requirements. These software
systems were developed to meet the standards of cGMP, GAMP and 21 CFR
Part 11. They were designed to include the quality and cGMP checks
necessary to make products with good manufacturing practices easy.