Quality Assurance Auditor in Toxikon Corporation, Bedford, USA
Received date: November 22, 2015 Accepted date: November 24, 2015 Published date: November 30, 2015
Citation: Sreelakshmi Chittamuru (2015) Focusing on Quality Assurance. J App Pharm 8:e102. doi: 1920-4159.1000e102
Copyright: © 2015 Sreelakshmi Chittamuru. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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The essential requirement for illuminate quality data and minimize using manual entry and increasing computational techniques over past three decades resulted in more significant advancements in the field of ‘Quality’. Journal of Applied Pharmacy is a peer reviewed Open Access Journal desire to get to the bottom of research and development in the field of Quality Assurance aspect mainly focusing on medical device Industries, pharmaceutical, Healthcare, and Technology Industries. This journal articles are peer reviewed by distinguished researchers and Industry experts, eminent and experienced delegates from academia who are working in quality assurance of the organization, academic and Institution research boards as editors and who work on superior quality of journals.
The main aim of journal is to publish high quality original research workflow data from project initiation to winding up the maintenance of the same project, data accuracy from the date of entry to the project closing in all aspects. Quality assurance results papers, viewpoint articles, technical papers, conceptual papers, case studies, literature reviews and general reviews related to the theory to serve the enthusiastic Bioinformatics research community.
The research areas include
• Quality Assurance
• Quality Control
• Method Validations
• Method Development
• Phase Audits
• System Audits
• Compliance Audits
• Regulatory Affairs
• Medical devices
• Institution regulations
• Animal welfare regulations
• Standard operating Procedures (SOPs)
• Corrective and Preventive Actions (Pharma, medical device, research and Healthcare sectors)
• Regulations (FDA, EPA, OECD, ICH, ISO e.tc.)
• CFRs ( Code for Federal Regulations)
• Clinical trial Monitoring
• Drug and Device approvals
• GLP studies (God Laboratory Practices)
• GMP (Good Manufacturing Practices)
• GDP (Good Document Practices)
• GCP (Good Clinical Practices)
• Device evaluationsq
• QbD (Quality by Design)
• Protocol Amendments & Deviation Reports (PADR)
• Chain of Custody in research study
The editorial board has right to reject or accept, or request for clarification or more about submitted article in form of comments on any research/review paper/abstract and if necessary, editing may constitute minor structural changes to the paper/ article. All articles published in an Open Access journal will be free for everyone to read, download, copy and distribute. We anticipate that our readers from all corners of the globe relish the experience of exploring knowledge of innovative work carried out in various fields of Bioinformatics through this journal.
We cordially invite enthusiastic Industry people, researchers, Academicians to submit their high quality articles from all aspects of Quality Assurance with regards to Pharma, medical device and Health care sector for review and possible publication in our inaugural issue. All authors who are in the article must agree on the content of the manuscript and its submission for publication in this journal before it is submitted to us.