Web Design and Quality Assurance

Web design and Web hosting

Present day’s software programming techniques have reached to a new height to cope with the ever-changing scenario of web design and web hosting principles. With the growing security concerns and increasing need of quality assurance, the task of web development has become increasingly challenging for today’s IT community. To ensure highest data security, new tools like PHP programming, .Net programming, etc. have evolved over the years. With rapid development in the e-commerce activity, web hosting has become the new way of existence for the business community. Mere knowledge on software programming is no more enough for achieving success in web development. In a single word, web design and web hosting calls for all the efficiency of software programming coupled with administrative skills, business awareness and a quality expertise on the multimedia art.

Phases of Web design

Basic understanding of HTML and Microsoft’s FrontPage, in addition to expertise on .Net programming and PHP programming, are essential in order to establish greater quality assurance in web development and web hosting fields. Following are the different phases of web design, if followed meticulously success can be achieved without much difficulty.

(a) Phase I: Defining Scope. Every web development project should have a defined scope outlining the need of gathering related information, risk and budget analysis, defining constraints, etc. The scope should be defined keeping in mind the business needs and existing technology of software programming.

(b) Phase II: Project Planning. Information gathered is now required to be re-evaluated with complete quality assurance guidelines. Formalities regarding web hosting also require to be conceptualized now.

(c) Phase III: Design and Testing. Now the actual designing should start. Testing also needs to be accomplished along every stages of web development in order to provide a consistent degree of quality assurance. There is a wide spread belief within the IT community that testing can be tasked at a later stage; but that is not fruitful and goes against the ethos of software programming technology.

(d) Phase IV: Production and Implementation. In this phase, content and layout are merged to give a final shape to the web development. Uses of PHP programming and .Net programming techniques are very important in this phase as they are the state-of-the-art tools for such purposes.

(e) Phase V: Maintenance and Updating. Once the web hosting is completed, maintenance and updating at regular intervals are mandatory to keep the website purpose-worthy.

Issues of Quality Assurance

Quality of design and quality of conformance are the two types of quality issues that we generally come across with the web development. Quality of design calls for a sound knowledge on the software programming techniques, especially knowledge of PHP programming and .Net programming are very much essential in order to ensure quality assured web development. Quality of conformance is the degree to which the design specifications are met during the development and implementation stages. Web site quality assurance plan should include the ways and means of design specification evaluation, procedures of audits and reviews, prescribed ways of monitoring defined standards, mechanism for error reporting and error tracking, etc.

Mansi Gupta
http://www.articlesbase.com/business-articles/web-design-and-quality-assurance-185234.html

"Web Design and Quality Assurance" için 4 Yorum

1
Gönderen: Sagar | Tarih: 27 February 2009

Can anybody explain the entire process of QA (Quality Assurance) in Pharma manufacturing?
please explain me anybody the process of QA. As I searched the entire web and not even one site is able to explain the process. even wikipedia is also failed to expalin. I know that Quality Assurance covers all activities from design, development, production, installation, servicing and documentation. But, I need stepwise explaination. So, If anybody knows the process kindly give me the answer.

2
Gönderen: RAMU | Tarih: 27 February 2009

HELLO

GIVING ANSWER IS VERY BIG FOR ENTIRE Q A
I THINK IT IS FOR ISO PURPOSE. THEN YOU HAVE
TO APPROACH AN ISO CONSULANTS.

IF YOU NEED MORE DETAILS ???????????!!!!!!!
I CAN…………..
References :

3
Gönderen: doctor | Tarih: 27 February 2009

Please visit the following web-sites :
whqlibdoc.who.int/publications/2004/9241546190.pdf
http://www.portal.nelm.nhs.uk/QA
http://www.ateliervision.de/gmp/quality_assurance.htm
strQuery=pharmaceutical+quality+assurance
http://www.ateliervision.de/gmp/quality_assurance.htm
You will get what you require.
References :
Google.

4
Gönderen: titanium007 | Tarih: 27 February 2009

Quality Assurance, as the name implies, assures that the quality of the product they produce passed standards and can be released to market. In Pharma setting, the QA process is quite strict; otherwise, the drug that they produce can harm instead of cure.

Usually, QA is a one big division in the company which comprises of sub groups: Chemistry Lab Dept, Microbiological Lab Dept, Physical Lab Dept, New Products Development Dept, Technical Services Dept, CGMP (Current Good Manufacturing Practices) Dept, and Documentation Dept. The labs do routine testing to ensure that correct quantity of the ingredients are added in the product, nutrients/active ingredients are on the right levels, no pathogens in the product, no foreign materials in the product, and that the product is of the right texture, density, etc. The New Products Development Dept do research to come up with new product lines and/or improve existing product lines. The Technical Services Dept is responsible for Validation Technology and Change Management in the plant. The CGMP Dept is responsible for maintaining the high standard of manufacturing the products. And the Documentation Dept is responsible for maintaining good documentation practices, following regulations, and keeping all the records.

Of course, these are just simple description. Details of their jobs are more complicated and need more time to explain.
References :
I work for a Pharma company.


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