How to Publish Your Articles, Research Work or News Release, Announcements about your company or your pharmaceutical product on http://whoguideline.blogspot.com
If you are interested in publishing your research papers or articles or new release on http://whoguideline.blogspot.com/ you can send us your articles for publishing on http://whoguideline.blogspot.com/
It is likely that when you publish your work or article on http://whoguideline.blogspot.com/ , your work will reach to our thousands of readers around the Glob.
Indeed ! our website is read and referred by almost every individual associated with pharmaceutical industry from USA ,Europe, and from all Asian Middle East, African countries, our website is day today read by almost all American pharmaceutical companies , there are chances that you will get noticed by good companies and you may get benefit of being known to world with your work.
let your work represent you !
Instead of you represent your work !
We have a policy to encourage and help pharma newbies , pharmacy students , an upcoming researcher , or a pharmaceutical company which really deserve a recognition from the world.
Following is the minimum requirement for qualifying your article for publication by us.
1. It should not be copied from other websites or any other places , it should be your genuine work , if at all you take down points from other places , you should write it in your words you should always add your ideas to your work.
2.You should submit a request to us for publication of your article through our website http://whoguideline.blogspot.com/ there is a Contact US link at bottom of website over there is a contact form you should fill the form and write a message for publishing your article along with following lines
"you have no objection in publishing your article "Title " "date" on http://whoguideline.blogspot.com/ and you wave off , copyright for it as well as all other rigths associated with your article time to time , forever and will not claim any right on it in any way".
3. Email us your article in word format by sending email to timesofpharma(@)gmail.com
Format of of your article
A.It should have a heading , as you do regularly with the name of original authors in this case obviously you and your colleagues and then a summary of your article , stating the usefulness and implementation / implications of your work / findings if at all are there etc.
B.Main article , not less than 500 words.
C.Authors Bio with contact details (Don't include your contact number , we don't need that)
D.Authority for publishing your article:
At the bottom of your word file you should write following lines.
"you have no objection in publishing your article "Title " "date" on http://whoguideline.blogspot.com/ and you wave off , copyright for it as well as all other rigths associated with your article time to time , forever and will not claim any right on it in any way".
By writing above lines in your word file you authorise us to publish your article on http://whoguideline.blogspot.com/ and you agree to wave off your copyrite claims and other rights forever and authorise us to syndicate your article through electronic distribution through RSS feeds to other online news agencies.
=====================================================================================================
Do you know now this website has become a most popular and most referred website in pharmaceutical industry and pharmaceutical companies and pharmaceutical manufacturers from all over the world ,for almost all topics related to Pharmaceutical Manufacturing , Pharmaceutical Regulatory Affairs and Good Manufacturing Practice for Pharmaceutical Manufacturing (c GMP guidelines ) and latest news and new drugs developments.
=====================================================================================================
You may also like following articles
What is a Site Master file of a pharmaceutical company
What is Generic Drug
What is Reference Listed Drug ? ( RLD )
What is Pharmaceutical Equivalents
What is Pharmaceutical Alternatives
What is Therapeutic Equivalents
What are Post Market studies
Why a drug is bound to protein, What is protein binding? What is drug absorption , distribution ?
Do Physical properties contribute to drug activity.
What is drug receptor , How a drug resistance occurs
Mechanism of drug resistance
What is drug interaction
Drug interaction, and its examples
What is first pass metabolism of a drug
What is What is 510(k) Clearances ?
What is 510(k) Clearances,
Premarket Notification for medical devices - PMN or 510(k)
What is a drug interaction
Examples of drug interactions
Antibiotic Definition and classification
Antibiotic Resistance and Antibiotic resistance mechanism
Antioxidants food supplements
Vitamin D Details on FDA cautions on accurate dosage of Vitamin D
What is an antibody? what is monoclonal and polyclonal antibodies?
Terminologies In vaccine Production
Multi stage testing of Virus vaccine production
Testing of vaccines at different stages of production
TESTING FOR ADVENTITIOUS AGENTS CELL PROPERTIES IN VIRAL VACCINE PRODUCTION
Enzyme linked immunosorbent assay ELISA
Raido Immuno assay
http://whoguideline.blogspot.com/2010/04/terminalogy-and-their-explanations.html
Pharmaceutical Aseptic Manufacturing Process Terms , Terminology and Definitions.
http://whoguideline.blogspot.com/2010/02/pharmaceutical-aseptic-manufacturing.html
Here are some articles which will be useful for you in further understanding of aspects of sterile dosage form manufacturing and regulatory affairs and good manufacturing practice in
pharmaceutical industry
Pharmaceutical Validation
Types of validations in pharmaceutical manufacturing
Requirements of documents for validation of sterilisation process
How to investigate OOS out of specification results
Determination of Phenol coefficient of a disinfectant
Sterility testing
Clean Room Classification
Time limitations in sterile pharmaceuticals processing
Aspects of validation of manufacturing process in sterile pharmaceuticals
Clinical Trials
Requirements of US FDA Inspections of Clinical Investigators of Clinical Trials
PROCEDURE OF AN INSPECTIONS OF CLINICAL TRIAL INVESTIGATOR BY US FDA HOW ARE CLINICAL INVESTIGATOR INSPECTIONS CONDUCTED?
US FDA INSPECTION OF CLINICAL INVESTIGATORS OUT OF UNITED STATES OF AMERICA
REPORTS AFTER AN INSPECTION OF A INVESTIGAOTR OF CLINICAL TRIALS
Controlling Pyrogens in injectable dosage forms
Media fill run process simulation aspects Validation of Aseptic Process and Sterilisation
New Drug Application (NDA) how to make a New Drug Application (NDA) to US FDA
Abbreviated New Drug Application (ANDA) What is ANDA , detailed information about ANDA preparation and submission to US FDA
How to make Investigational New Drug (IND) Application to US FDA
Drug applications submission to us fda Over the counter Drugs OTC drugs
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
Electronic record in pharmaceutical manufacturing industry
Good manufacturing practice in pharmaceutical industry
Pharmaceutical industry pharmaceutical companies and FDA latest updates
Here is an interesting article on world wide pharmaceutical industry and making a carrier in one of pharmaceutical companies article on Pharmaceutical Industry pharmaceutical industry
Find a Job in Pharmaceutical Company -->JOBS IN PHARMA INDUSTRY<---
To Find Pharmaceutical jobs and make a Pharmaceutical careers see here pharmaceutical companies
Here are some interesting articles on Quality assurance systems for pharmaceutical company
Quality assurance in pharma industry
Quality by design concept for pharmaceutical industry
Quality by design concept in pharmaceutical industry an explanation
Useful Books For Pharmaceutical Manufacturers and Pharmaceutical Professionals
No comments:
Post a Comment