Manufacturing Facility Webinar on Standard Operating Procedures

Cary, NC – With the quality and purity of dietary supplements
recently being called into question, establishing a quality system is
paramount to ensuring products are safe. Writing Standard Operating
Procedures (SOPs) is the first step in creating this system for a
manufacturing facility. InstantGMP and EAS Consulting Group will host a
webinar, “SOPs: The Foundation of a Quality System,” on Tuesday, February 24th at 1 PM EST.

The webinar will cover:

  • Why SOPs are needed
  • Information that should be included in a SOP
  • Examples of how SOPs would be applied at different steps in the production process of a dietary supplement

“InstantGMP has always been committed to making GMP compliance easy,” said Dr. Richard Soltero, President of InstantGMP.  “Partnering
with EAS on this webinar is one more way we can help dietary supplement
manufacturers come to grips with understanding these requirements.”

“Documentation is the cornerstone to any firm’s
quality system,” said Dean Cirotta, President of EAS. “Without
well-written, thorough and appropriate SOPs, a firm cannot achieve GMP
compliance. Therefore, we are pleased to partner with InstantGMP to
provide this very valuable training on the importance of Standard
Operating Procedures in an FDA regulated environment.”

The cost to attend is $25 and interested parties can register
for the event via Eventbrite –
https://www.eventbrite.com/e/sops-the-foundation-of-a-quality-system-tickets-15460433573

About InstantGMP
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.

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