“QUALITY SYSTEM” TO HANDLE COMPLAINT AND RECALL IN PHARMACEUTICALS: A REVIEW
Journal Title: Journal of Drug Discovery and Therapeutics - Year 2013, Vol 1, Issue 2
Abstract
‘Quality' means compliance with statutory or agreed standards rather than grade of materials and workmanship. Manufacturers use many controls to make sure that the products they produce are safe. Sometimes, for many different reasons, a product may be manufactured and sold which may make some people ill or injure them, or is in violation of the legislation. When an unsafe product has left the control of the manufacturer, after complaint products must be recall from the market. Good manufacturing practice ensures that products released for distribution are of the appropriate quality. Medicinal products are distributed to the general public without any alteration of their properties. "For those drugs for which environmental assessments have been required, there has been no indication of environmental effects due to flushing," says Bloom. Despite the safety reasons for flushing drugs, some people are questioning the practice because of concerns about trace levels of drug residues found in surface water, such as rivers and lakes, and in some community drinking water supplies. So allow the public to bring unused drugs to a central location for proper disposal.
Authors and Affiliations
Bhupender Kumar Nimbiwal*| Department of Quality Assurance, Seth G. L. Bihani S. D. College of Technical Education, IPSDR, Sri Ganganagar, Rajasthan, India – 335001, Prof. Rajesh Kumar Dholpuria| Department of Quality Assurance, Seth G. L. Bihani S. D. College of Technical Education, IPSDR, Sri Ganganagar, Rajasthan, India – 335001, Ramchandra| Department of Quality Assurance, Seth G. L. Bihani S. D. College of Technical Education, IPSDR, Sri Ganganagar, Rajasthan, India – 335001, Monish Sharma
Keywords
Related Articles
- EP ID EP1348
- DOI -
- Views 516
- Downloads 27
FORMULATION AND EVALUATION OF IMMEDIATE RELEASE EMTRICITABINE & TENOFOVIR DISOPROXIL FUMARATE TABLET
The main purpose of the present study is to formulate and evaluate once daily an immediate release tablet of Emtricitabine and Tenofovir disproxil fumarate using different disintegrants. Preformulation studies were perfo...
REVIEW ON IN-VITRO ANTIOXIDANT SCREENING ASSAYS
Oxygen, an element indispensable for life, can under certain circumstances, adversely affect the human body. The oxygen consumption inherent in cell growth leads to the generation of a series of reactive oxygen species (...
A rare case of flupirtine induced loss of speech.
Anarthria can be caused by CNS depressant drugs but flupirtine consumption leading to it, is not documented till date. Since it is a drug with unique properties and is being more commonly used by practitioners, caution n...
FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF CEFUROXIME AXETIL
In this investigation, fast dissolving tablets of Cefuroxime Axetil were prepared using different super disintegrants. A wet granulation method was used as direct compression method unable to formulate dispersible table...
NOVEL DRUG DELIVERY SYSTEM-NANOEMULSIONS: A RECENT REVIEW
Nanoemulsions are the emulsions of O/W type, having the size range of several microns. Nanoemulsions are clear, thermodynamically stable, isotropic liquid mixtures of oil, water, surfactant and co-surfactant. They are pr...