Cary, NC – EAS Consulting Group, LLC., an FDA regulatory consulting, auditing and
training firm has joined forces with electronic batch record software
developer InstantGMP, Inc. to offer GMP Orientation Training to new
customers. The GMP orientation will be tailored to the dietary
InstantGMP works primarily with growing supplement
manufacturers new to FDA regulations and good manufacturing practices.
All InstantGMP customers receive an hour-long overview of GMP as part of
the training package included with their software subscription.
The electronic batch record software guides users through GMP workflows
, and the orientation provides a springboard for understanding what the
FDA expects and how InstantGMP helps manufacturers meet compliance.
”We are especially proud of our association with the EAS
Consulting Group” said Dr. Richard Soltero, President of InstantGMP.
“Their expertise and experience in GMP consulting will go a long way to
helping our customers meet their GMP goals.”
Dean Cirotta, President of EAS said, “Given that both EAS and
InstantGMP have a common goal of improving the GMP compliance of our
clients, we are pleased to promote the use of InstantGMP software, as it
is a great tool to assist dietary supplement firms comply with the many
detailed requirements of FDA’s GMP regulations.”
Both companies hope that the combination of the software and
GMP expertise will help growing businesses better understand GMP and why
it is paramount in creating quality products.
Develops cloud-based electronic batch record software and SOPs that
reinforce Good Manufacturing Practices. These software systems were
developed to meet standards specific to the pharmaceutical industry and
were recently updated for the Dietary Supplement industry. Please visit
the Resource Center at InstantGMP.com for articles, videos, and tutorials
on GMP compliance.
About EAS Consulting Group, LLC
EAS Consulting Group
specializes in FDA regulatory matters in the supplement,
pharmaceutical, medical device, food, tobacco and cosmetics industries,
including assistance in tailored compliance training, 483 responses,
mock-FDA audits, labeling compliance, and more. EAS is staffed with former industry experts and FDA officials who have expertise in both FDA policies and enforcement.