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Last updated on April 16, 2014 at 7:15 EDT

Latest Good manufacturing practice Stories

2014-03-31 12:29:27

The Emerson Quality Program(SM) turns over a new leaf MANCHESTER, N.H., March 31, 2014 /PRNewswire/ -- Emerson Ecologics, LLC, the leading distributor of over 275 professional brands of vitamins, supplements and natural health products to healthcare practitioners, announced today that they are raising the bar in their Emerson Quality Program(SM) (EQP). The key change to the program includes a revised assessment of every brand distributed by Emerson in order to demonstrate present...

2014-03-19 23:02:33

Pharmaceutical manufacturers are required by the FDA to train personnel in FDA quality system requirements and procedures. Now manufacturers can train their staff for significantly less money, in their own office, with a new training video developed by a former FDA investigator. Falls Church, VA (PRWEB) March 19, 2014 Quality Systems Training DVD for Drugmakers **FDAnews DVD Training Course** http://www.fdanews.com/QualityDrugDVD Pharmaceutical manufacturers are required by the FDA to...

2014-02-27 23:01:07

Memory Supplement Makers Earn Recertification of NSF Good Manufacturing Practices Madison, WI (PRWEB) February 27, 2014 Quincy Bioscience announces that its headquarters, shipping, and manufacturing locations have all been recertified as Good Manufacturing Practices (GMP) facilities registered by NSF International for 2014. Earning GMP registration from NSF International verifies that Quincy Bioscience’s facilities have the proper methods, equipment, facilities, and controls in place...

2014-02-20 23:27:59

Private Label Nutraceuticals, global leader in dietary supplement contract manufacturing, achieves Good Manufacturing Practices (GMP) certification. Atlanta, GA (PRWEB) February 20, 2014 Private Label Nutraceuticals, prominent contract manufacturer of high quality private label dietary supplements and nutritional products, receives GMP Certification through ASI Food Safety Consultants, leader in food safety audits since 1948. GMP regulations are set by the US Food and Drug...

2014-02-11 04:22:08

DETROIT, Feb. 11, 2014 /PRNewswire/ -- VPCI, Inc., a provider of consultation services to the pharmaceutical industry, is pleased to announce the collection of additional reimbursements from the U.S. Food and Drug Administration (FDA) resulting from PDUFA fee waiver requests. In a fairly narrow set of qualifying circumstances, drug manufacturers may qualify for refunds of PDUFA fees paid. Continuing to act on behalf of its clients, VPCI provided assistance and coordinated the entire...

2014-02-10 23:04:28

Regulatory Compliance Associates Inc. (RCA), a life sciences consultancy focused on quality, regulatory and technical consulting, announces Mr. Andrew Harrison has accepted a role as Vice President & General Counsel. Pleasant Prairie, WI (PRWEB) February 10, 2014 Regulatory Compliance Associates Inc. (RCA), a life sciences consultancy focused on quality, regulatory and technical consulting, announces Mr. Andrew Harrison has accepted a role as Vice President & General Counsel....

2014-01-22 23:27:30

With the high cost and strict handling requirements for products entering clinical development, the logistics of clinical trial supplies are clearly more critical than ever. The Best Practices for Managing Clinical Trial Materials webinar will help trial sponsors see that an effective materials process, based on effective and sound principles, can become the foundation for a successful trial. Falls Church, VA (PRWEB) January 22, 2014 Best Practices for Managing Clinical Trial Materials...

2014-01-07 08:31:40

MILLBURY, Mass., Jan. 7, 2014 /PRNewswire/ -- BellHawk Systems www.BellHawk.com today announced the availability of a 21 CFR Part 11 compliance module. This enables the use of the BellHawk inventory and work-in process tracking software in FDA regulated pharmaceutical manufacturing and distribution applications that need to be validated to comply with FDA good manufacturing practices (GMP). (Logo: http://photos.prnewswire.com/prnh/20140107/PH41520LOGO ) A major issue for small- to...

2013-12-16 16:25:28

EAST RUTHERFORD, N.J., Dec. 16, 2013 /PRNewswire/ -- Cambrex Corporation (NYSE: CBM, "Cambrex") announced that the US Food and Drug Administration (FDA) completed an inspection of Cambrex's active pharmaceutical ingredient (API) manufacturing facility in Charles City, Iowa. The inspection found the site to be compliant with the principles and guidelines of Good Manufacturing Practice (GMP) and no Form 483 observations were issued. The US FDA authorities inspected the facility from...

2013-12-10 23:30:04

Former FDA official brings extensive experience in quality and compliance King of Prussia, PA (PRWEB) December 10, 2013 Tunnell Consulting, Inc. today announced that Anthony A. Charity, who served in the U.S. Food and Drug Administration (FDA) for more than twenty years, has joined the firm as a Managing Consultant, Quality and Compliance. “Anthony Charity’s experience at the FDA enables him to provide our life sciences clients with invaluable help in understanding good...