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GOOD DOCUMENTATION PRACTICE (REF NO: LS/20091124)




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Public seminar
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Price: – HKD300 per head
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Duration: 2 hours
(9:00 a.m. – 11:00 a.m.)
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Ref: LS/20091124

PHARMACEUTICAL GMP SEMINAR – WORKSHOP 1: GOOD DOCUMENTATION PRACTICE (REF NO: LS/20091124)

GMP has been a well known industry standard in the pharmaceutical manufacturing companies. The QC control lab is one of the key parts in contributing the success of the GMP system. Through this seminar series, we hope to share with the industry our experiences in the QC lab control for the GMP factory.

Workshop 1: Good Documentation Practices

  • What is Documentation Practices?
  • What kinds of records are required to control?
  • How to handle electronic record?
  • Exercise Section

DATE: 24 November 2009 (Tuesday)
TIME: 9:00 a.m. to 11:00 a.m.
VENUE:

SGS Training Room
12/F, Metropole Square, 2 On Yiu Street,
Siu Lek Yuen, Shatin, NT, Hong Kong

For location details, please click the microscope on the right side of the screen

MEDIUM OF INSTRUCTION: Cantonese
SPEAKER OF THE SEMINAR: Dr. Claren Woo (Section Manager from Healthcare and Pharmaceutical Department under Life Science Services. She received her PhD in Chemistry and has been involved in the Pharmaceutical and Personal Care related services for around 5 years.  She is a HOKLAS approval signatory and well familiar with the quality system in both ISO 17025 and GMP guideline.)
SEMINAR FEE: HKD300 per head
CONTACT: Alan Ng
Phone: (852) 2609 9611 ext 3353
Fax: (852) 2603 7577
Email
APPLICATION DEADLINE: 20 November 2009 (Friday)

For online enrolment, please click the flash “ONLINE BOOKING/CLICK HERE”.

CONTACT