Facility validation

GOOD MANUFACTURING PRACTICE (cGMP)
1

Dear All,
I am very much intrested to know about all GMP guidelines(USFDA, PICS, MHRA, EU, MCC, TGA, ANVISA etc.) for the facility, equipment, environmental requirements of a pharmaceutical industries(sterile & Non sterile dosage forms)

Could you please give me some suggestions how can I got this information through net (any special sites, web sites etc.)

Thanks in advance

Naveen.

2

Pl Find Herewith The Matter For Mhra Guidelines

Regulations to Act 101.DOC (416.5 KB)

3

Dear Gagandeep kaur,
Thank you for your help, if you any other guidelines please forward me
Have a niceday
Bye.

4

Dear Gagandeep kaur,
Thank you for your help, if you any other guidelines please forward me
Have a niceday