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 supplement industry.
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 that is included with their software subscription. The electronic batch record software guides users through GMP workflows and the orientation provides “who, what, when, where and most importantly, why” of the process.
”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 the Instant GMP 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 integral to creating quality products.
InstantGMP, Inc. 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 trainings, 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.