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February 2010
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Feb 2010
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W07 21 22 23 24 25 26 27
W08 28 1 2 3 4 5 6


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Wed, Nov 25, 2009


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31

1
• WORKING THROUGH DRUG DEVELOPMENT - Winter School
• Introduction to Effective Medical Writing
2
• ANNUAL CONFERENCE ON INTERNATIONAL SPORTS LAW - A Year in Sports Law
• WORKING THROUGH DRUG DEVELOPMENT - Winter School
• Introduction to Effective Medical Writing
3
• WORKING THROUGH DRUG DEVELOPMENT - Winter School
• The Drug Development Process - From Discovery to Commercialization
• Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
4
• WORKING THROUGH DRUG DEVELOPMENT - Winter School
• PHARMACEUTICAL REGULATORY AFFAIRS IN THE MIDDLE EAST Including Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Qatar, Saudi Arabia, Syria, UAE and Yemen
• The Drug Development Process - From Discovery to Commercialization
• Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
5
• WORKING THROUGH DRUG DEVELOPMENT - Winter School
• PHARMACEUTICAL REGULATORY AFFAIRS IN THE MIDDLE EAST Including Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Qatar, Saudi Arabia, Syria, UAE and Yemen
• The Drug Development Process - From Discovery to Commercialization
6

7

8
• Good Clinical Practices (GCP)
• Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
• FDA Inspections of Clinical Data Systems
• Practical Methods for Project Management
9
• THE US DRUG APPROVAL PROCESS
• Good Clinical Practices (GCP)
• Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
• FDA Inspections of Clinical Data Systems
• Practical Methods for Project Management
10
• 5th Annual Drug Delivery Systems Conference
• THE US DRUG APPROVAL PROCESS
• Good Clinical Practices (GCP)
• QA/QC Strategy for Biopharmaceuticals and Biologics

11
• 5th Annual Drug Delivery Systems Conference
• QA/QC Strategy for Biopharmaceuticals and Biologics
• Adverse Drug Events - Reporting & Regulatory Requirements
12
• QA/QC Strategy for Biopharmaceuticals and Biologics
• Adverse Drug Events - Reporting & Regulatory Requirements
13

14

15

16

17

18
• Effective Laboratory Safety Management

19
• Effective Laboratory Safety Management

20

21

22
• Writing Effective Standard Operating Procedures and Other Process Documents
• FDA Inspections - What to Expect and How to Prepare
• Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
23
• Writing Effective Standard Operating Procedures and Other Process Documents
• FDA Inspections - What to Expect and How to Prepare
• Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
• 8th Cold Chain Management & Temperature Control Summit
24
• Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
• Writing in the Regulated Environment When English Is Your Second Language
• Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
• 8th Cold Chain Management & Temperature Control Summit
25
• The international conference on Early Disease Detection and Prevention (EDDP)
• Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
• Writing in the Regulated Environment When English Is Your Second Language
• Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
• 8th Cold Chain Management & Temperature Control Summit
26
• The international conference on Early Disease Detection and Prevention (EDDP)
• The Bacteriophage in Biology, Biotechnology and Medicine
27
• The international conference on Early Disease Detection and Prevention (EDDP)

28
• The international conference on Early Disease Detection and Prevention (EDDP)
• Pittcon 2010 Conference and Exposition
1
• euroPLX 42 Valletta
• Adverse Drug Events - Reporting & Regulatory Requirements
• Good Clinical Practice for Medical Device Investigations
• Biostatistics for Non-Statisticians
• Pittcon 2010 Conference and Exposition
2
• euroPLX 42 Valletta
• Adverse Drug Events - Reporting & Regulatory Requirements
• Good Clinical Practice for Medical Device Investigations
• Biostatistics for Non-Statisticians
• Stability Programs for Product Shelf Life - From Development to Approval
• Pittcon 2010 Conference and Exposition
3
• Biostatistics for Non-Statisticians
• Stability Programs for Product Shelf Life - From Development to Approval
• Good Clinical Practice Auditing
• The Drug Development Process - From Discovery to Commercialization
• Pittcon 2010 Conference and Exposition
4
• Good Clinical Practice Auditing
• The Drug Development Process - From Discovery to Commercialization
• Pittcon 2010 Conference and Exposition
5
• Regulatory T cells in inflammatory and infectious diseases: new horizons for old friends
• The Drug Development Process - From Discovery to Commercialization
• Pittcon 2010 Conference and Exposition
6

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