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

Overview of the Requirements on WFI in the EU, USA and Japan

17/10/2013 00:22
Again and again, the question...

Article on the consequences of non-compliance

17/10/2013 00:21
Wockhardt stock drops after...

WHO publishes revised draft on GTDP for pharmaceutical starting material

17/10/2013 00:19
The WHO guide on Good trade...

FDA Launched Secure Supply Chain Pilot Program

17/10/2013 00:17
The U.S. Food and Drug...

EMA publishes revised dossier-submission requirements for active-substance master files

17/10/2013 00:15
The European Medicines Agency...
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