קטגוריה: PDA - העמותה לקידום המדע והטכנולוגיה הפרמצבטית בישראל , כנסים
Annual Meeting of Israel Chapter of PDA

 

העמותה לקידום וטכנולוגיה הפרמצבטית בישראל
תאריך: 3 ינואר 2010
מיקום הקורס:  גן ארועים הגן השקוף, שפיים
שפת הקורס: עברית
משך הפעילות: יום לימודים מלא
שעות: 15:30-21:00
התכנסות והרשמה: 15:00
נקודות זכות: 0
מק''ט: P10700
 

Annual Meeting
of The Israel Chapter of PDA
Sunday, 3 January 2010

15:30-21:00h
The Shefayim Conventions Center (Transparent Garden)
מרכז הכנסים והקונגרסים שפיים (הגן השקוף)

A professional and social event and a festive dinner

Program:

Duration
Topic
Speaker
15:30 - 16:00
Registration, Coffee and Vendors Exhibits

16:00 – 16:10

President's Welcome

Dr. Raphy Bar
BR Consulting

16:10– 16:20

Treasurer's Report

Karin Baer
Omrix Biopharmaceuticals Ltd.

16:20 – 17:00

Dilemmas in the Management of the Current Influenza Pandemic ("Swine Flu")

Prof. Dan Engelhard
Head of Pediatrics
Hadassah University Hospital;
Head, Management Team for Epidemics Ministry of Health

17.00 – 17:20
Bylaws of The Israel Chapter of PDA and Elections

Dr. Raphy Bar
President of PDA Chapter

17.20 – 18:30
Cocktail Reception and Vendors Exhibits
18:30 – 19:00 Part A: UPDATES


Current GMP Legislation in Israel


Upcoming Changes Regarding Importation and Batch Release of Medicinal Products

Dr. Rachel Karpel
PCI Ltd


Dr. Mimi Kaplan
MOH

19:00 – 19:40 Part B: Panel Discussion
Positions and comments
on GMP Legislation in Israel
Representatives of manufacturers, importers, wholesalers, Clalit Health Services, The Pharmaceutical Society of Israel and MOH
Moderated by
Dr. Rachel Karpel
PCI Ltd

Click here to see all panel participants
19:40– 20:00

Hot Quality and Regulatory Topics: Update on International PDA’s Regulatory and Quality Affairs Committee

Karen Ginsbury
PCI Ltd

20:00 – 21:00
Festive Dinner

The evening will include a festive dinner and vendors exhibition with the opportunity to network with colleagues from pharmaceutical, biotech and
medical device companies.

Exhibitors:

Who should attend:

This promises to be a special meeting addressing aspects behind and around the "scenes" of the manufacturing of the finished drug product: development process, pre-clinical studies, clinical trials, patent and regulatory affairs. The meeting is not to be missed and is suitable for participants from the following disciplines:

  • Research and Development
  • Quality Assurance / Compliance  
  • Quality Control and Laboratories  
  • Manufacturing  
  • Regulatory Affairs
  • Pharmacists 
  • Clinical Trials  
  • IT Systems

Participation Fees:
PDA members - 300 NIS
Non members - 495
NIS  

Registration is mandatory, please register here

For map please click here





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