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good manufacturing practices


Deerland Enzymes Awarded Site Reference Number from NNHPD of Canada

by Shari Barbanel | December 5, 2014

Deerland Enzymes (Kennesaw, GA) has announced that the company has received a notice of acceptance from Health Canada Natural and Non-prescription Health Products Directorate (NNHPD) for a Foreign Site Reference Number (FSRN). Deerland Enzymes is among a select group of companies located in the United States chosen to participate in the NNHPD’s pilot program that ...

Deerland Enzymes Receives FAMI-QS Certification

by Angela Santoriello | November 21, 2014

­ Deerland Enzymes (Kennesaw, GA) announced that the company has received the Feed Additives and Premixtures Quality System (FAMI-QS) certification for its manufacturing facility in Kennesaw, GA. The audit was conducted by Eurofins, an international leader in the assessment and certification of quality and safety management systems, reported the company. The state-of-the-art quality certification is ...

InstantGMP Adds Data Transfer Tool for QuickBooks

by Angela Santoriello | November 3, 2014

InstantGMP (Cary, NC), a company that develops cloud-based electronic batch record software and SOPs specific to the dietary supplement industry, created an import tool that interfaces with QuickBooks Desktop Applications, reported the company. Users can export inventory and purchase order data from InstantGMP and upload it to QuickBooks instead of updating it in multiple applications. ...

Paragon Labs GMP Certified — Again

by Angela Santoriello | August 25, 2014

Paragon Laboratories (Torrance, CA) reported it has been re-certified by the Natural Products Association (NPA) for meeting a high level of compliance with association’s standard for good manufacturing practices (GMPs) of dietary supplements. Paragon Laboratories is a nutritional and dietary supplement contract manufacturer specializing in the turnkey manufacture and packaging of tablets, capsules and powders, ...

GMPs: One Year Later

by Kate Quackenbush | June 1, 2011

As FDA audits have begun, the consensus is that the industry still has a long way to go proving its compliance, but it’s making a concerted effort to reach that goal. Setting a three-year timeline for industry-wide good manufacturing practices (GMP) compliance seemed ample, but as it has passed and U.S. Food and Drug Administration (FDA) ...

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