2. PRESENTED TO
SIMIN SHABNAM LOPA
B.PHARM & M.PHARM (RU)
LECTURER DEPARTMENT OF
PHARMACY,VARENDRA UNIVERSITY
PRESENTED BY
SAIMA AKTER
ID NO. 151211046
3. GMP
GMP refers to the Good
Manufacturing Practice. According to
WHO, “Manufacturing practices
which result in good quality finished
product, and has adequate
considerations for safety for the
employees, is recognized as Good
Manufacturing Practice(GMP)”
4. CGMP
GMP is sometime referred to as
“cGMP”. The “c” stands for “current”
reminding manufacturers that they
must employ methods and systems
which are up-to-date in order to
comply with the regulation.
5. “MANUFACTURING”
WHO defines the term “manufacturing” as,
“all operations involved in the production
of a drug, including processing,
compounding, formulating, filling,
packaging and labeling.”
6. THE NECESSITY OF GMP
To follow national legislature
To follow WHO certification on the
quality of pharmaceutical products.
For export: Bangladesh is now a drug
exporting country therefore, regulation
of other countries are to be obeyed for
exporting.
7. BMR
BMR- Batch Manufacturing Record
Dispensing
of FDF
Production
process
BMR
