Welcome to My Website

 

Hi Friends! Everybody must have heared a great proverb "Knowledge is Power". Exactly... But many people of us are not aware of either the information source or complete details of information to improve knowledge. Even I also faced the same in my starting days of career as many people were not interested to share their knowledge to the people in thirsty. This made me to think about a need to create a place to share the knowledge among ourselves. That is what the purpose of this website....

 

Thus this website is designed with the theme of "A PLACE WHERE KNOWLEDGE IS SHARED". Here you can find the valuable information related to GMP, Regulatory Guidances, Newsletters, USFDA Warning Letters, Various Audit Observations, current trends in Pharmaceutical/ Biotech/ Food industries etc.

 

My aim through this website is to have a day where nobody depends on anybody to get information to improve knowledge.....

Regards,

 

One among you....

SEETHARAM KANDARPA...







 

 

Visitor's Notice

Who can be Visitor?

This website may be useful to share knowledge among the people such as:

  • Professionals of Quality Assurance, Quality Control, Production, Engineering, Warehouse, Regulatory Affairs & other fuctions working in Pharmaceutical/ Food/ Biopharmaceutical Industry.
  • Individuals who are interested to know about GMP environment.
  • Persons who want to educate others or support others to improve their knowledge to become a Better Professional in their field of work.

 

Come here to get knowledge and share the same to the people who are not aware of.....

Dear Users,

 

To view updated/ new content, click tag "WHAT IS NEW"....

 

 

 

 

Poll

Do you feel this website useful?

Yes (1,068)
65%

No (286)
17%

Don't know (287)
17%

Total votes: 1641

News

More Inspections by USFDA in 2014

29/01/2014 23:58
U.S. President Barack Obama...

"Reception denied!" - the new FDA "Refuse-to-Receive" Guidance for Generics Applications

28/01/2014 23:55
When reviewing submitted...

Update: Electronic Submission of Marketing Authorisation Dossiers

28/01/2014 23:51
"How and to whom shall I...

How to submit an Active Substance Master File?

22/01/2014 23:47
As part of the authorisation...

Good Practice Guidelines for Blood Establishments as a Co-Operation between the EDQM/CoE and the EU Commission published

22/01/2014 23:44
In November 2013 the European...
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