International Good Manufacturing Practice Training Program 2016 (updated 18 Jan 2016)

Star InactiveStar InactiveStar InactiveStar InactiveStar Inactive
 

MOPI GMP Training 2016 - Brochure Version 1.0

The course training program consists of 9 principal modules and 6 additional modules, each of 3 days duration. These modules cover the essential principles of Good Manufacturing Practice (GMP). Participants are expected to gain an understanding of current requirements and future international trends within the pharmaceutical industry. Each participant will be assessed on their level of participation within classroom discussion, assignments and their level of competence in achieving the course objectives. Assignments will be case studies based on actual events that have occurred in the pharmaceutical industry.

Aims and Objectives

The aim of the course is to provide an in-depth understanding of international GMP and the knowledge and know-how to be able to implement Good Manufacturing Practices in the work place.

Who Should Attend?

  • Key Personnel in any Aspect of GMP & Quality Management
  • Managers
  • Engineers
  • Executives
  • Quality Practitioners
  • Any member of a pharmaceutical factory who is from Research and Development, Quality and Production will find this program relevant and beneficial to their job function

Trainers

This course has been developed by SeerPharma and trainers are provided by, SeerPharma (Singapore) Pte Ltd. All SeerPharma trainers hold higher education degrees with a minimum of a Bachelor’s degree and have a number of years of industry experience in Quality Management or Production Management roles in major and multinational companies. They have experience in all international regulatory standards including FDA, EU, PIC/S, TGA and ISO. The trainer for each module will have specific expertise in that subject matter. SeerPharma is Australia’s and Asia Pacific’s premier training & consulting group offering integrated consulting, training and technical services to Australia and the Asia Pacific region to meet all international regulatory standards.

Download the brochure and registration form to view the overall program details.

Note: Certificates endorsed by the National Pharmaceutical Control Bureau, Ministry of Health, Malaysia will be awarded to participants upon successful completion of each module.

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti, 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

DISCLAIMER

The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

Mobile Web :

Newsletter Subsription

Site Last Modified

  • Last Modified: Monday 18 February 2019, 12:11:14.
© Copyright 2018 . All Rights Reserved National Pharmaceutical Regulatory Agency NPRA

Main Menu English

Choose Your Language