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November 2009
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Nov 2009
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Thu, Nov 26, 2009


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1

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• Advances & Challenges in Label-Free Technologies for Drug Discovery
• PHARMACEUTICAL REGULATORY AFFAIRS IN LATIN AMERICA

3
• Advances & Challenges in Label-Free Technologies for Drug Discovery
• PHARMACEUTICAL REGULATORY AFFAIRS IN LATIN AMERICA
• Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
4
• PHARMACEUTICAL REGULATORY AFFAIRS IN LATIN AMERICA
• Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
• Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
5
• Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
• Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
6
• Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
7

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• Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval
10
• Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval
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• Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval
12
• INHALED DRUG DELIVERY (IDD)

13
• INHALED DRUG DELIVERY (IDD)

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• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development
• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development

17
• SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development
• LATEST DEVELOPMENTS IN PHARMACOVIGILANCE

18
• Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing
• LATEST DEVELOPMENTS IN PHARMACOVIGILANCE
• REGULATORY BASICS by HALLORAN Consulting Group
19
• Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing
• Adverse Drug Events - Reporting & Regulatory Requirements
• Effective Risk-Based Applications of Drug cGMPs and Validation Requirements for Cosmetics and OTC Drug Products
20
• Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing
• Adverse Drug Events - Reporting & Regulatory Requirements
• Effective Risk-Based Applications of Drug cGMPs and Validation Requirements for Cosmetics and OTC Drug Products
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• INTRODUCTORY OVERVIEW OF THE PHARMACEUTICAL INDUSTRY

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• Active Pharmaceutical Ingredient (API) and Drug Product Specifications
1
• Active Pharmaceutical Ingredient (API) and Drug Product Specifications
2
• Active Pharmaceutical Ingredient (API) and Drug Product Specifications
3
• Dermatological Advances 2009 Conference
• RISK MANAGEMENT - Applying it and meeting the Challenges for Industry
• Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
• How to Develop an Effective Complaint Handling and Post Market Surveillance Program for Drugs and Devices
• ADVANCED CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group
4
• Dermatological Advances 2009 Conference
• Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
• How to Develop an Effective Complaint Handling and Post Market Surveillance Program for Drugs and Devices
• RISK MANAGEMENT - Applying it and meeting the Challenges for Industry
• ADVANCED CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group
5

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