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Lallemand Receives USP’s GMP Certificate for Canadian Production Facilities

by Shari Barbanel | September 11, 2017

Lallemand Health Solutions announced that both of its Canadian probiotic production plants in Montreal and Mirabel successfully passed the United States Pharmacopeia (USP) Quality Systems Good Manufacturing Practice (GMP) audit. The company thus has become the first probiotic production facilities to receive this quality certificate. “Such achievement illustrates our long-standing commitment to quality and demonstrates ...

NPA to Hold “The FDA Experience” Training Event

by Shari Barbanel | June 28, 2017

The leading experts in the field of the natural products industry and former U.S. Food and Drug Administration (FDA) officials Daniel Fabricant, PhD, president and CEO of Natural Products Association (NPA) and Corey Hilmas, MD, PhD, NPA’s senior vice president of scientific and regulatory affairs, will host a five-day training dubbed “The FDA Experience” on ...

Frutarom Health Increases Phytopharmaceutical Capacity

by Shari Barbanel | February 14, 2017

Frutarom Health BU (Israel) reports it will strengthen focus on its phytopharmaceutical business in 2017. This follows the 2016 acquisition of Extrakt Chemie GmbH & Co.KG, in Stadhagen, near Hannover, Germany, and supports the rapid growth of its pure phytopharmaceutical line. The global size of the phytopharmaceutical market is estimated at €750-850 million (Euro) (approximately ...

InstantGMP Releases Software Update

by Shari Barbanel | May 26, 2016

InstantGMP, Inc.’s (Cary, NC) InstantGMP MES v3.0 electronic batch record software has gone through a transformative aesthetic and functionality update that is designed to make GMP (good manufacturing practice) compliance for dietary supplement manufacturers easier. “Our work with dietary supplement producers has helped us design a much more user-friendly manufacturing system application for them, said ...

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 ...

New Quick-Melt Technology available at ProTab Labs

by Angela Santoriello | November 12, 2014

ProTab Laboratories (Foothill Ranch, CA) introduced its newly developed and proprietary Qk-MeltTech technology for the manufacture of quick-melt tablets that dissolve rapidly in the mouth, as quickly as 45 seconds, without the need of water. ProTab’s new technology offers an excellent alternative to consumers who experience difficulty swallowing traditional tablets with or without water, reported ...

Proprietary Compliance

by Janet Poveromo | October 6, 2014

Nutrition Industry Executive magazine’s October issue profiled some of the latest proprietary ingredients offered to manufacturers. Here, suppliers discuss how GMPs and other regulatory scrutiny affect their company and sales. Shaheen Majeed, marketing director with Sabinsa Corporation: Sabinsa manufactures its products under strict cGMP (current good manufacturing practice) manufacturing standards and is willing to share ...

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, ...

Quality Deliverance

by Rajiv Leventhal | November 1, 2012

As today’s regulatory environment tightens, working with a reliable contract manufacturer brings added benefits as companies look to expand.As companies are always looking to grow their product lines, market share, customer base and, of course, sales, there are many factors they take into consideration when looking to contract manufacturers: cost savings, speed, quality and skill ...

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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