Monthly Newsletter: March 2005
This newsletter has been published by the International Biopharmaceutical Association www.ibpassociation.org . Please note this publication does not give any medical advice.
The project is sponsored by Kriger Research - CRO and Training Services ( www.kriger.com ) and ClinQua CRO (www.clinqua.com )
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Special Event:
Medical Device and Pharmaceutical
Manufacturing Seminar Series
When: March 23, 2005; 2-5 p.m.
Where:
Purdue University Office of Engagement
Building 10
6640 Intech Blvd., Suite 120
Indianapolis, Indiana 46278-2012
317.275.9301
The first of a three part series on Balancing Compliance with Good Business
Practices is designed to help Manufacturing, Quality, and Regulatory
Executives and their teams maintain solid business practices by fusing
technology with compliance requirements. Joseph Vinhais, one of the country's
leading authorities on the subject of Regulatory Compliance, will present the
latest trends and best practices in medical device and pharmaceutical
manufacturing.
This session deals with Risk Management in Life Science Manufacturing . By
successfully leveraging technology and risk management, Regulatory, Quality,
and Manufacturing executives can align business performance and corporate
metrics and help their organizations meet compliance and enforcement goals.
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Clinical Research Scientist, link Montreal , Canada
Clinical Research Associate, link Montreal , Canada
Clinical Research Associate, link Canada & USA
Clinical Research Associate I, link Toronto, Canada
Clinical Research Associate, link Mechelen , Belgium
Clinical Research Associate, link Johannesburg , South Africa
Clinical Research Associate, link Budapest , Hungary
Clinical Research Associate, link Cary , USA
Clinical Research Associate, link Czech Republic
Clinical Research Associate, link Munich , Germany
Clinical Research Associate, link Cambridge , USA
Clinical Research Coordinator, link Cambridge , USA
Clinical Research Associate, link Pennsylvania , USA
Clinical Research Associate, link New Jersey , USA |
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Biostatistician, link Toronto , Canada
SAS Programmer Analyst, link Ottawa , Canada
Biostatistician, link Toronto , Canada
Manager, Clinical Data Management, link Toronto , Canada
Clinical Data Coordinator I-III, link Reading , England
Clinical Data Coordinator III, link Eatontown , USA
Clinical Data Processor, link Victoria , Canada
Clinical Data Coordinator, link Victoria , Canada
Biostatistician, link Lenexa , USA
Statistical Programmer, link Cary , USA
Clinical SAS Programmer, link California , USA |
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Drug Safety Specialist, link Montreal , Canada
Quality Systems Manager, link Toronto , Canada
Regulatory Affairs Associate, link Kirkland , Canada
Quality Assurance Manager, link Ottawa , Canada
Quality Assurance Auditor, link USA & Canada
Director Drug Safety Center , link Mannheim , Germany
Process Analyst, link Charlottesville , USA
Global Regulatory Affairs, link Reading , England
Quality Assurance Auditor, link United Kingdom
Auditor GCP Compliance, link California , USA
Clinical Data Coordinator, link California , USA
Clinical Data Manager, link Massachusetts , USA
Quality Assurance Specialist, link Maryland , USA
Associate I, Regulatory Affairs, link Toronto , Canada |
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Manager, Market Access, link Montreal , Canada
Manager Business Development, link London , Canada
Business Development Analyst, link Vancouver , Canada
Manager, Marketing & Communications, link Ottawa , Canada
Project Manager, link Ottawa , Canada
Business Coordinator, link United Kingdom
Business Development Director, link Cambridge , USA |