CGMPs assure accurate design, monitoring, and control of manufacturing processes and facilities and assure the identity, strength, quality, and purity of drug products by adequately control manufacturing operations. CGMP requirements were established to be flexible in order to allow each manufacturer to implement the necessary controls by using scientifically sound design, processing methods, and testing procedures. The flexibility in these regulations allows companies to use modern technologies
AREAS OF FOCUS:
a) Contamination/Cross Contamination
b) Consistency in Manufacturing throughout the lifecycle.
c) Mix Up and Data Integrity
d) Risk Management and Good Sciences
e) Quality Culture and Quality Matrics
• Mr. Sultan Ghani
• Dr. Saif Ur Rehman Khattack
• Dr. Iftikhar Jafri
• Ms. Roohi B. Obaid
• Dr.M.Raza Shah
DOWNLOAD REGISTRATION FORM
Center for Bioequivalence Studies and Clinical Research(CBSCR)
HEJ Research Institute of Chemistry.
International Center for Chemical and
Biological Sciences, University of Karachi-(ICCBS)
TIMING: 9:00AM – 5:00PM
PKR 1000 only for Students.
PKR 3000 only for Professionals.
Send scan copy of Filled Registration form and Pay order/ Bank Deposit slip (Account # 1146-0101-8338, UBL, University of Karachi Branch, Account Title: -DIRECTOR CBSBR- at the Official CBSCR Email I.D.
If, Registration Fee in cash: Submit your cash along with filled registration form at reception of HEJ Research Institute of Chemistry, ICCBS, University of Karachi.
NOTE: Bring your Original N.I.C and Registration form and Bank Deposit Slip/ Pay order on the day of Session. Registration Forms are also available on face book Page.
For further details contact:
Cell #: +923351272780
Face book Page/ Group:
Center for Bioequivalence Studies and Clinical Research