John Wiley and Sons Ltd, July 2008, Pages: 297
Medical Product RegulatoryAffairs: Pharmaceuticals, Diagnostics, MedicalDevices Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory
FirstWord Publishing, June 2011
This Report
- Medical Science Liaison personnel
- Medical and Scientific Advisors
- Medical and Scientific Affairs personnel
- Medical communications experts
- KOL development leaders
- RegulatoryAffairs
FirstWord Publishing, March 2012, Pages: 58
and territory management
- Marketing, brand and sales management
- Medical Science Liaison
- IT procurement
- Business development
- Regulatory and government affairs
- Medical communication
Key Questions
Research Facts Ltd, April 2009, Pages: 200
and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are several hundred Contract Research Organisations in Europe. This report profiles the Top 100 of them
Bioplan Associates Inc., April 2008, Pages: 190
challenge. Since that time she has enjoyed a variety of roles in medicalaffairs, clinical development, drug safety and regulatoryaffairs which has provided a broad foundation and experience. She is a Fellow
Research Facts Ltd, April 2009, Pages: 107
and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Europe with experience and expertise in cancer. This report
John Wiley and Sons Ltd, May 2011, Pages: 296
Cost-Contained Regulatory Compliance: For the Pharmaceutical, Biologics, and MedicalDevice Industries This book guides the reader through FDA regulation guidelines and outlines a comprehensive
Research Facts Ltd, April 2009, Pages: 58
development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Germany and France. This report profiles
Timely Data Resources, Inc., May 2012
Fourteen years primary market research experience in the pharmaceutical, biotechnology, medicaldevice, drug delivery and diagnostics industries, with industry experience at Syntex, Theratech, Genelabs
John Wiley and Sons Ltd, June 2010, Pages: 272
research in the academia and industry. She is the Director of Global Research Pharma Canada. She conducts Good Clinical Practice (GCP) audits for the pharmaceutical, biotech, and medicaldevice industries worldwide
Research Facts Ltd, April 2009, Pages: 106
to both growth in drug development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Europe
Research Facts Ltd, April 2009, Pages: 108
in drug development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Europe with experience
Research Facts Ltd, April 2009, Pages: 48
development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in the United Kingdom. This report profiles
Research Facts Ltd, April 2009, Pages: 42
development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Eastern Europe. This report profiles
Research Facts Ltd, April 2009, Pages: 44
growth in drug development and the increasing use of outsourcing by pharmaceutical, biotechnology and medicaldevice companies.
There are numerous Contract Research Organisations in Europe
FirstWord Publishing, Oct 2011, Pages: 48
- Health Technology Assessment professionals
- Health Policy professionals
- Pricing & Reimbursement teams
- Government and regulatoryaffairs analysts
- Marketing research/business intelligence managers
Espicom Business Intelligence Ltd, Feb 2012, Pages: 60
and MedicalDevices Safety Authority (Medsafe). This authority regulates all products used for a therapeutic purpose, using the Medicines Act 1981 and Regulations 1984. Medsafe is the regulatory agency
John Wiley and Sons Ltd, Dec 2010, Pages: 800
of pharmaceutical medicine. New content includes chapters and coverage on regulatory updates, increasing international harmonization, transitional and probabilistic approaches to drug development, the growing
Decision Resources, Inc., May 2011
.
- Issues affecting the pharmaceutical industry in Europe: European Commission consultation on drug pricing and reimbursement; intense criticism of the French regulatory authority; reimbursement reduction
Contact Canada, Jan 2012
Canadian Medical Technologies Products & Industry Guide 2012 The national directory of the Medical technologies industry in Canada. Profiles on 660 Medicaldevice companies, diagnostic systems
