Monday, January 24, 2011

Technical Module Review Part II

Frankly speaking, too much classroom sessions were really like my university time. Huh, those days are bored enough but still my friends and I managed to cope with. The content somehow have helped us to be excited on we are going to listen next. Here, the summary on what I went through for 8 days. How bored the topic it was but the general knowledge still can be gained form all those speakers. The clinical research information was good enough for me to realize that the career opportunity in particular study was available in Malaysia. Credit to CReST EvendZ (CE).

Intellectual Property (IP) Protection,


Good Laboratory Practice (GLP)

+

Good Clinical Practice (GCP)

+

Good Manufacturing Practice (GMP)

+

Good Clinical Data Management Practice (GCDMP)


 =

 Good Regulatory Practices (GxPs)

p/s:I don't even know before that drug development procedure will take many years to be completed, lol.

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