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November 2009
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Tue, Nov 24, 2009


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• BIO-Europe 2009
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• BIO-Europe 2009
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• BIO-Europe 2009
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• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development
• GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India
• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development
• Generic Medicine: IP / Legal and Regulatory Issues
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• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development

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• GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India
• Generic Medicine: IP / Legal and Regulatory Issues
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• European Regulatory Affairs
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• European Regulatory Affairs
• GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India
• Generic Medicine: IP / Legal and Regulatory Issues
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• BIOLOGICAL EVALUATION OF MEDICAL DEVICES - Understand The New Approach To Biological Evaluation And Its Practical Application
• Non-Clinical Safety Sciences and Their Regulatory Aspects
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• BIOLOGICAL EVALUATION OF MEDICAL DEVICES - Understand The New Approach To Biological Evaluation And Its Practical Application
• Non-Clinical Safety Sciences and Their Regulatory Aspects
• SUPPLIER QUALITY MANAGEMENT - How well do you know your Suppliers and Supply Chain?

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• Non-Clinical Safety Sciences and Their Regulatory Aspects
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• Non-Clinical Safety Sciences and Their Regulatory Aspects
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• Non-Clinical Safety Sciences and Their Regulatory Aspects
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• THE EU COSMETICS DIRECTIVE AND THE NEW COSMETICS REGULATIONS

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