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October 2009
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Oct 2009
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Fri, Nov 20, 2009


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27

28
• THE MEDICAL DEVICE AUTUMN SCHOOL: - 5 Day Residential Course - Boston, USA - From Concept to Market
• ADVANCED PHARMACOVIGILANCE
• Periodic Safety Update Reports - A 2 Day Practical Meeting
29
• 3rd Smoking Cessation Conference
• THE MEDICAL DEVICE AUTUMN SCHOOL: - 5 Day Residential Course - Boston, USA - From Concept to Market
• ADVANCED PHARMACOVIGILANCE
• RISK MANAGEMENT - Applying it and meeting the Challenges for Industry
• Periodic Safety Update Reports - A 2 Day Practical Meeting
• The role of pharmacy in the management of depression
30
• STRATUM CORNEUM VI - RESIDENTIAL COURSE
• Outsourcing in Clinical Trials East Coast
• 3rd Smoking Cessation Conference
• THE MEDICAL DEVICE AUTUMN SCHOOL: - 5 Day Residential Course - Boston, USA - From Concept to Market
• ADVANCED PHARMACOVIGILANCE
• RISK MANAGEMENT - Applying it and meeting the Challenges for Industry
• Microarray Data Analysis Webcast Series: 2-Channel Gene Expression Analysis
1
• PHARMACOKINETICS - Workshop for Beginners
• STRATUM CORNEUM VI - RESIDENTIAL COURSE
• Prefilled Syringes 2009
• THE MEDICAL DEVICE AUTUMN SCHOOL: - 5 Day Residential Course - Boston, USA - From Concept to Market
• Practical Methods for Project Management
• Quality System Regulation for the Medical Device & Biotech Industries
2
• PHARMACOKINETICS - Workshop for Beginners
• STRATUM CORNEUM VI - RESIDENTIAL COURSE
• Prefilled Syringes 2009
• THE MEDICAL DEVICE AUTUMN SCHOOL: - 5 Day Residential Course - Boston, USA - From Concept to Market
• Practical Methods for Project Management
• Quality System Regulation for the Medical Device & Biotech Industries
3

4

5
• PDA's 4th Annual Global Conference on Pharmaceutical Microbiology
• Validation of Computer Systems
• Analytical Method Validation for Quality Assurance of Pharmaceutical Products
• Patent and Other Intellectual Property Law for the Life Sciences Industry
6
• ESSENTIAL GUIDE TO CLINICAL TRIALS REGULATIONS
• PDA's 4th Annual Global Conference on Pharmaceutical Microbiology
• Pharmaceutical & Medical Device Risk-Sharing & Value-Based Pricing & Reimbursement Schemes
• Validation of Computer Systems
• Analytical Method Validation for Quality Assurance of Pharmaceutical Products
• Patent and Other Intellectual Property Law for the Life Sciences Industry
• The EU Clinical Trial Directive
• Effective Quality Assurance Auditing for FDA Regulated Industries
7
• ESSENTIAL GUIDE TO CLINICAL TRIALS REGULATIONS
• PDA's 4th Annual Global Conference on Pharmaceutical Microbiology
• 2nd Annual Clinical Trials in India and China Conference
• Pharmaceutical & Medical Device Risk-Sharing & Value-Based Pricing & Reimbursement Schemes
• Practical GCP Compliance Auditing of Trials & Systems
• The EU Clinical Trial Directive
• Effective Quality Assurance Auditing for FDA Regulated Industries
• Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
• QA/QC Strategy for Biologics and Biopharmaceuticals
8
• PDA's 4th Annual Global Conference on Pharmaceutical Microbiology
• 2nd Annual Clinical Trials in India and China Conference
• Clinical Outsourcing Alliances in Central & Eastern Europe
• Clinical Statistics for Nonstatisticians
• ABRIDGED LICENCE APPLICATIONS - Generics, Well Established Use & Mixed Product Licences
• Practical GCP Compliance Auditing of Trials & Systems
• Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
• QA/QC Strategy for Biologics and Biopharmaceuticals
• Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
• European Filing & Registration Procedures
• How to Implement Risk Management Principles and Activities Within a Quality Management System
9
• 2nd Annual Clinical Trials in India and China Conference
• Clinical Statistics for Nonstatisticians
• ABRIDGED LICENCE APPLICATIONS - Generics, Well Established Use & Mixed Product Licences
• Practical GCP Compliance Auditing of Trials & Systems
• Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
• QA/QC Strategy for Biologics and Biopharmaceuticals
• Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
• European Filing & Registration Procedures
• How to Implement Risk Management Principles and Activities Within a Quality Management System
• TLRs (Toll-like receptors), NLRs (Nod-like proteins) and RLRs (RIG-like receptors), pathogens sensors of innate immunity

10

11

12
• European Manufacturing Strategies 2009 (EMS 2009)
• REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 1 - An Overview of Pharmaceutical Regulatory Affairs For Support Staff
• Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
• Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
• Writing Effective Standard Operating Procedures and Other Process Documents
• How to Monitor Clinical Trials for GCP Compliance
• Process Validation for Medical Devices
• 2009 Aspetic Processing Training Program Session 5, Week 1
13
• MipTec 2009
• SUCCESSFUL IMPLEMENTATION OF MANUFACTURING SITE CHANGES - A Practical Guide
• REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2
• Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
• Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
• Writing Effective Standard Operating Procedures and Other Process Documents
• How to Monitor Clinical Trials for GCP Compliance
• Process Validation for Medical Devices
• Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
• 2009 Aspetic Processing Training Program Session 5, Week 1
• Strategic Manufacturing Awards 2009
14
• 5th Modern Drug Discovery & Development Summit
• MipTec 2009
• Good Monitoring Practices for Medical Devices
• 6th Annual Pain Management Conference
• THE ROLE OF THE RESPONSIBLE PERSON - MHRA Review on Good Distribution Practice
• THE ROLE OF THE RESPONSIBLE PERSON - MHRA Review on Good Distribution Practice
• THE BORDERLINE BETWEEN MEDICINES AND FOODS
• Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
• Process Validation for Medical Devices
• Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
• The Drug Development Process - From Discovery to Commercialization
• SUCCESSFUL IMPLEMENTATION OF MANUFACTURING SITE CHANGES - A Practical Guide
• 5th Modern Drug Discovery & Development Summit
• 2009 Aspetic Processing Training Program Session 5, Week 1
• Safety Biomarkers in Drug Development
15
• MipTec 2009
• Cleantech Forum XXIV- Delhi
• Good Monitoring Practices for Medical Devices
• 5th Modern Drug Discovery & Development Summit
• 6th Annual Pain Management Conference
• Synaptic Inhibition in Health and Disease
• QUALITY BY DESIGN - Making QbD real and cost effective for both R&D and Manufacturing
• Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
• An Introduction to Product Information Management (PIM)
• The Drug Development Process - From Discovery to Commercialization
• FDA Inspections: What To Expect And How To Prepare
• Pharmaceutical Production Batch Record Review
• 5th Modern Drug Discovery & Development Summit
• 2009 Aspetic Processing Training Program Session 5, Week 1
• Elispot follow-up meeting
• Microarray Data Analysis Webcast Series: Comparative Genomic Hybridization Analysis
16
• 5th Modern Drug Discovery & Development Summit
• Synaptic Inhibition in Health and Disease
• Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
• An Introduction to Product Information Management (PIM)
• The Drug Development Process - From Discovery to Commercialization
• FDA Inspections: What To Expect And How To Prepare
• Pharmaceutical Production Batch Record Review
• QUALITY BY DESIGN - Making QbD real and cost effective for both R&D and Manufacturing
• 5th Modern Drug Discovery & Development Summit
• 2009 Aspetic Processing Training Program Session 5, Week 1
17

18

19
• 3rd Annual Clinical Forum
• 2009 PDA Visual Inspection Forum
• 5th Annual Biosimilars Conference
• US Regulatory Affairs
• Maximizing Global Recruitment and Retention
• Biostatistics for Non-Statisticians
20
• 3rd Annual Clinical Forum
• 2009 PDA Visual Inspection Forum
• 5th Annual Biosimilars Conference
• US Regulatory Affairs
• Maximizing Global Recruitment and Retention
• Biostatistics for Non-Statisticians
21
• 3rd Annual Clinical Forum
• 2009 PDA Visual Inspection Forum
• 5th Annual Biosimilars Conference
• US Regulatory Affairs
• Biostatistics for Non-Statisticians
• Stability Testing of Proteins, Peptides & Other Biomolecules
• Improving Investigator Site Performance
• Safety Biomarkers in Drug Development
22
• 2009 PDA Visual Inspection Forum
• US Regulatory Affairs
• Stability Testing of Proteins, Peptides & Other Biomolecules
• Improving Investigator Site Performance
• Understanding Regulatory & Clinical Information Systems During Product Development
• Auditing and Qualifying Suppliers and Vendors
• AN INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVES - Gain a Comprehensive Understanding of the Regulatory Requirements
• Realigning Priorities of Internal Audit to Add Value
• Using BI To Thrive In Challenging Economic Times
• Induced pluripotent stem cells: production and utility in regenerative medicine
• INTRODUCTION TO CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group
23
• 2009 PDA Visual Inspection Forum
• Food Allergy: a global perspective
• Understanding Regulatory & Clinical Information Systems During Product Development
• Auditing and Qualifying Suppliers and Vendors
• AN INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVES - Gain a Comprehensive Understanding of the Regulatory Requirements
• INTRODUCTION TO CLINICAL PROJECT MANAGEMENT - 2-Day workshop by HALLORAN Consulting Group
• MHRA Abridged Applications - Getting it right first time
24

25

26
• PDA Workshop: The Shifting Paradigm in Process Validation
• MICROBIOLOGY FOR PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRIES
• Best Practices for an Effective Cleaning Validation Program
• Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
• Design Control for Medical Device Professionals
• THE MEDICAL DEVICE DIRECTIVE, QUALITY SYSTEMS AND CONFORMITY ASSESSMENT (INCLUDING AUDITING)
• Personalized Medicine, In an Era of Health Care Reform, Colloquium
27
• PDA Workshop: The Shifting Paradigm in Process Validation
• MICROBIOLOGY FOR PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRIES
• Best Practices for an Effective Cleaning Validation Program
• Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
• Design Control for Medical Device Professionals
• PHARMACOVIGILANCE INSPECTIONS FOR THE VETERINARY INDUSTRY
• TECHNICAL FILE DOCUMENTATION AND REVIEW
• Personalized Medicine, In an Era of Health Care Reform, Colloquium
28
• PDA Workshop: The Shifting Paradigm in Process Validation
• RISK MANAGEMENT : A CORE PROCESS
• Design Validation, Verification, and Risk Analysis for Medical Device Professionals
• Process Validation for Drugs and Biologics
• PHARMACOVIGILANCE INSPECTIONS FOR THE VETERINARY INDUSTRY
29
• An Introduction to VETERINARY STATISTICS
• AN ESSENTIAL GUIDE TO PHARMACOVIGILANCE
• Design Validation, Verification, and Risk Analysis for Medical Device Professionals
• Process Validation for Drugs and Biologics
• Introduction to Effective Medical Writing
• FDA Inspections of Clinical Data Systems
• AUDITING ACTIVE MEDICAL DEVICES ~ WHATS NEW
• Antibody Partnering & Technology Summit
30
• An Introduction to VETERINARY STATISTICS
• Introduction to Effective Medical Writing
• FDA Inspections of Clinical Data Systems
• STERILE MEDICAL DEVICES
• Antibody Partnering & Technology Summit
31

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