TITLE

Vision system targets drugs

AUTHOR(S)
Wilson, Andrew
PUB. DATE
June 2004
SOURCE
Vision Systems Design;Jun2004, Vol. 9 Issue 6, p13
SOURCE TYPE
Periodical
DOC. TYPE
Article
ABSTRACT
Discusses the inspection solutions for the pharmaceutical industry developed by electronics company Systech International to comply with the regulations of the U.S. Food and Drug Administration (DFA). Requirements of the 21 CFR Part 11 regulation of the DFA; Reason for the development of inspection solutions for the pharmaceutical industry by Systech International Features of the inspection solution of the company.
ACCESSION #
13486633

 

Related Articles

  • OCV supports FDA-compliant packaging line. Hardin, Winn // Vision Systems Design;Dec2007, Vol. 12 Issue 12, p35 

    The article deals with the installation of vial-packaging line from Systech International which is compliant with the U.S. Food and Drug Administration (FDA) 21 CFR standards. The manufacturing line includes two monochrome optical-character-verification (OCV) machine-vision inspection stations...

  • As I See It. DICKINSON, JAMES G. // Medical Marketing & Media;Aug2013, Vol. 48 Issue 8, p32 

    The article presents the author's views on the importance for pharmaceutical industry marketers to promote products on the Internet and on how the U.S. Food and Drug Administration monitors what companies are doing in cyberspace.

  • The path to electronic-records compliance. Conley, Jim // Pharmaceutical Processing;Jan2000, Vol. 17 Issue 1, p114 

    Reports on the United States Food and Drug Administration's (FDA) issuance of warning letters to pharmaceutical manufacturers signifying its intention to enforce the Electronic Records and Signature Rule. Impact of the rule in the archival, storage and retrieval of raw analytical data;...

  • Getting Manufacturing Process Control Down PAT. McGee, Patrick // Drug Discovery & Development;Jun2005, Vol. 8 Issue 6, p33 

    The article reports that the U.S. Food and Drug Administration (FDA) is emphasizing on the use of process analytical technology (PAT) that could help the pharmaceutical industry update some manufacturing practices that have not changed in decades. In most manufacturing plants, quality control...

  • Are Your Drugs Safe? Shute, Nancy // U.S. News & World Report;10/15/2007, Vol. 143 Issue 13, p61 

    This article examines issues of product safety within the pharmaceutical industry. Just 10 of the 21 multivitamins tested met the quality claims on the label, ConsumerLab.com reported in January 2007. Several had significantly more or less of the active ingredients than promised; one was...

  • Early Studies Aim to Spur Development. Wechsler, Jill // Applied Clinical Trials;Mar2006, Vol. 15 Issue 3, p32 

    No abstract available.

  • Pragmatic Materials.  // Pharmaceutical Technology;Aug2005, Vol. 29 Issue 8, p18 

    Reports on the warning letter issued to Solon, Ohio-based Pragmatic Materials Inc., a company that repackages active pharmaceutical ingredients for sale to pharmacies for compounding, by the U.S. Food and Drug Administration. Criticisms issued to the company for listing manufacturers' expiration...

  • FDA Posts Q5E Biotech and Biological Products Comparability Guideline. Rios, Maribel // Pharmaceutical Technology;Aug2005, Vol. 29 Issue 8, p18 

    Reports that the U.S. Food and Drug Administration has posted the Q5E Guidance for Industry, Comparability of Biotechnological/Biological Products. Support of the International Conference on Harmonization to the guideline; Features of the pharmaceutical standard; Usefulness in assisting...

  • Business Efficiency and Regulatory Compliance. Souza, Doug; Danese, John; Constantinou, Dennis // Pharmaceutical Technology;2005 Supplement, ps6 

    Focuses on the business efficiency and regulatory compliance in the pharmaceutical industry in the U.S. Complexity of the compliance challenge as a result of significant changes at Food and Drug Administration and other federal government agencies; Need for all companies to comply with...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics