DATE
30 Oct - 1 Nov 2017
Monday - Wednesday
8:30am - 5:30pm
LOCATION
Marina Mandarin Singapore
6 Raffles Boulevard
Marina Square
Singapore 039594
"Understanding EudraLex in the context of premises, processes, products, procedures and people"
ISPE Singapore Affiliate is delighted to bring to Singapore Europe's most popular GMP Course!
Please note that the number of attendees for this training course is strictly limited. We strongly recommend that you reserve your places as soon as possible, to avoid disappointment. Following is a brief write-up about the trainers and links with detailed information on the course.
Why should I attend this training?
Europe's most popular GMP course!
- Tutors with real credibility and experience to bring GMP to life with examples and real life stories
- Training designed to reach all learning styles and preferences
- Fantastic detailed reference material to take away and to become instantly useful
- Bring your questions and have the free consultancy of tapping into great experience from helpful tutors
- This course repeatedly achieves the highest customer satisfaction level of any of our courses, with 95% of delegates rating it "very good" or "excellent"
- This course now forms an entry level GMP training requirement for our very popular Pharmaceutical Quality Management Systems Auditor/Lead Auditor Training Program
- An ideal starting point for our modular QP training program
Click here to view the program details >>
The Trainers
Mr Mike Halliday
BSc (Pharm), MRPharmS, PGDip
- Executive Vice President, NSF Health Sciences - Member of the Royal Pharmaceutical Society of Great Britain Member of the Industrial Pharmacist Group
- Qualified Person by assessment via the permanent provisions of EU Directive 75/319/EEC
- Extensive pharmaceutical manufacturing management and QA experience gained over 20 years working for three major international pharmaceutical manufacturers culminating in the post of Associate Director - Global Audit and Compliance for Wyeth Europa
- Broad experience with the manufacture of a wide range of parenteral and non-parenteral dosage forms
- Extensive experience in international QA auditing of a wide range of pharmaceutical manufacturers of most dosage forms and specialist distributors in Europe, Middle East, America and Asia Pacific
- International experience with factory management and new factory start up and validation Project management experience with technology transfer
- Honorary lecturer at the University of Strathclyde
Mrs Liz Allanson
BSc(Pharm), MRPharmS
- Qualified Person under the Transitional Provisions since 1985
- ISO 9001 Lead Auditor since 1993
- Held roles including Manager and Inspector, GMP Inspection unit at UK Medicines and Healthcare products Regulatory Agency (MHRA) from 1986 - 2004
Testimonials
"It is a fun and relaxed way of knowing much more about GMP."
Elma Snijder, Solvay, The Netherlands
"Well planned. Professional tutors. It has been a pleasure. Good with the group works and the social arrangements."
Mie Weibel, PEC, Denmark
"Excellent structure, use of experience and engagement."
John Facer, 3M Healthcare, UK
"Coming from another industry, this course was a really good overview of GMP."
Richard Griffiths, Bard Pharmaceuticals, UK
Registration Fees
|
Member |
Non-member |
|
| Early Bird* / Group Rate** | S$1,895 | S$2,195 |
| Regular | S$2,195 | S$2,495 |
* Early Bird valid until 30 June 2017
**for groups of 3 and more
If you have any questions or need assistance with your registration, please contact Kristina Autenrieth at ispesingaffiliate@gmail.com .
