Events Calendar
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Use this page to view Upcoming Events, jump to Advanced Search, or begin to Post Events.
Events By Name
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Upcoming Events
- March 17 - 19, 2010 - Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
- March 17 - 18, 2010 - Sterilization Procedures: Technology, Equipment & Validation
- March 17 - 18, 2010 - Purchasing Controls in the Medical Device Industry
- March 19, 2010 - Understanding Disinfectant Qualification Studies – How to avoid errors
- March 22 - 23, 2010 - Overview of FDA Regulatory Compliance for Medical Devices
Events By Month
Click on a month below to view its associated events.
March 2010 [+] (43 total)
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Adverse Drug Events - Reporting & Regulatory Requirements
March 1 - 2, 2010
Berlin GERMANY
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Good Clinical Practice for Medical Device Investigations
March 1 - 2, 2010
Malvern PA UNITED STATES
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Biostatistics for Non-Statisticians
March 1 - 3, 2010
Berlin GERMANY
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Biopharma Freeze-Drying Course
March 1 - 3, 2010
Amsterdam NETHERLANDS
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Business, Project and Compliance Risk
March 2, 2010
Online DE UNITED STATES
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Setting Up and Running a Tougher Supplier Audit Program
March 2, 2010
Wilmington DE UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
March 2 - 3, 2010
Malvern PA UNITED STATES
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Good Clinical Practice Auditing
March 3 - 4, 2010
Malvern PA UNITED STATES
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The Drug Development Process - From Discovery to Commercialization
March 3 - 5, 2010
Berlin GERMANY
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FDA Inspections: What to Expect and How to Prepare
March 3, 2010
Online Webinar DE UNITED STATES
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Asia Pharma R&D Leaders 2010
March 4 - 5, 2010
Shanghai CHINA
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Introduction to Molecular Biology Techniques
March 8 - 10, 2010
Malvern PA UNITED STATES
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Good Clinical Practices (GCP)
March 8 - 10, 2010
Berlin GERMANY
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
March 8 - 9, 2010
Malvern PA UNITED STATES
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The EU Clinical Trial Directive
March 9 - 10, 2010
Malvern PA UNITED STATES
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How to Prepare for a Systems-based Inspection - Understanding FDA's Risk-Based Inspections Approach
March 9 - 10, 2010
Malvern PA UNITED STATES
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
March 10 - 12, 2010
Malvern PA UNITED STATES
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Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
March 11 - 12, 2010
Malvern PA UNITED STATES
Read more... -
How to Develop an Effective Complaint Handling, and Post Market Surveillance Program for Drugs and Devices
March 11 - 12, 2010
Malvern PA UNITED STATES
Read more... -
European Filing & Registration Procedures
March 11 - 12, 2010
Malvern PA UNITED STATES
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Performing Investigations for Environmental Excursions
March 11, 2010
Palo Alto CA UNITED STATES
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Preparing the CMC Section for NDAs/CTDs/INDs
March 15 - 16, 2010
Costa Mesa CA UNITED STATES
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Cleanroom Microbiology for the Non-Microbiologist
March 15 - 16, 2010
Malvern PA UNITED STATES
Read more... -
Labeling and Labeling Controls for Medical Devices
March 15 - 16, 2010
Malvern PA UNITED STATES
Read more... -
Clinical Trials Design for Medical Devices
March 15 - 16, 2010
Malvern PA UNITED STATES
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Validation of Computer Systems
March 15 - 16, 2010
Berlin GERMANY
Read more... -
Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
March 17 - 19, 2010
Malvern PA UNITED STATES
Read more... -
Sterilization Procedures: Technology, Equipment & Validation
March 17 - 18, 2010
Malvern PA UNITED STATES
Read more... -
Purchasing Controls in the Medical Device Industry
March 17 - 18, 2010
Malvern PA UNITED STATES
Read more... -
Understanding Disinfectant Qualification Studies – How to avoid errors
March 19, 2010
Palo Alto CA UNITED STATES
Read more... -
Overview of FDA Regulatory Compliance for Medical Devices
March 22 - 23, 2010
Dublin IRELAND
Read more... -
Project Management for Phase 1 & 2 Clinical Trials
March 22 - 23, 2010
Malvern PA UNITED STATES
Read more... -
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Pharmaceutical Production Batch Record Review
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
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How to comply with recent expectations for Extractables /Leachables testing for Biologics
March 22, 2010
Palo Alto CA UNITED STATES
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Root Cause Analysis for CAPA
March 24 - 26, 2010
Dublin IRELAND
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Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
March 24 - 26, 2010
Costa Mesa CA UNITED STATES
Read more... -
Project Management for Phast 3 & LCM (Life Cycle Management) of the Drug Development Process
March 24 - 25, 2010
Malvern PA UNITED STATES
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Optimization of Freeze-Drying Cycles Using Modulated Differential Scanning Calorimetry (MDSC)
March 25, 2010
UNITED STATES
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Effective Quality Assurance Auditing for FDA Regulated Industries
March 29 - 30, 2010
Dublin IRELAND
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Selecting and Managing CROs
March 29 - 30, 2010
Malvern PA UNITED STATES
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cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
March 30, 2010
Palo Alto CA UNITED STATES
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Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Process Responsibilities
March 31, 2010 - April 1, 2010
Malvern PA UNITED STATES
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April 2010 [+] (37 total)
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Active Pharmaceutical Ingredient (API) and Drug Product Specifications
April 7 - 9, 2010
King of Prussia PA UNITED STATES
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Project Management for Phase 1 & 2 Clinical Trials
April 8 - 9, 2010
Dublin IRELAND
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Quality System Regulation for the Medical Device & Biotech Industries
April 8 - 9, 2010
King of Prussia PA UNITED STATES
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SBS 16th Annual Conference & Exhibition
April 11 - 15, 2010
Phoenix AZ UNITED STATES
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Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
April 12 - 13, 2010
Dublin IRELAND
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Best Practices for Facilities and Utilities Design, Qualification and Monitoring - Applying the Life-Cycle Concept
April 12 - 13, 2010
King of Prussia PA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
April 12 - 13, 2010
Berlin GERMANY
Read more... -
How to Monitor Clinical trials for GCP Compliance
April 12 - 13, 2010
King of Prussia PA UNITED STATES
Read more... -
Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
April 12 - 14, 2010
Berlin GERMANY
Read more... -
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
April 14 - 16, 2010
Berlin GERMANY
Read more... -
Effective Qualification and Monitoring of Processing Equipment and their Control Systems
April 14 - 15, 2010
King of Prussia PA UNITED STATES
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
April 15 - 16, 2010
Berlin GERMANY
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Patent and Other Intellectual Property Law for the Life Sciences Industry
April 15 - 16, 2010
Costa Mesa CA UNITED STATES
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Biostatistics for Non-Statisticians
April 19 - 21, 2010
King of Prussia PA UNITED STATES
Read more... -
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
April 19 - 21, 2010
Dublin IRELAND
Read more... -
QA/QC Strategy for Biopharmaceuticals and Biologics
April 19 - 21, 2010
Berlin GERMANY
Read more... -
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
April 19 - 20, 2010
Berlin GERMANY
Read more... -
Effective Quality Assurance Auditing for FDA Regulated Industries
April 19 - 20, 2010
Costa Mesa CA UNITED STATES
Read more... -
Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
April 20 - 21, 2010
King of Prussia PA UNITED STATES
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Troubleshooting Problematic Cycles and Formulations
April 20, 2010
UNITED STATES
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Process Validation for Medical Devices
April 21 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
The Drug Development Process - From Discovery to Commercialization
April 21 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Introduction to Statistical Analysis of Laboratory Data
April 22 - 23, 2010
King of Prussia PA UNITED STATES
Read more... -
Introduction to Effective Medical Writing
April 22 - 23, 2010
Berlin GERMANY
Read more... -
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
April 22 - 23, 2010
Dublin IRELAND
Read more... -
2nd Annual Drug Development Congress
April 22 - 23, 2010
London UNITED KINGDOM
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Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
April 22 - 23, 2010
Berlin GERMANY
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Validation of Computer Systems
April 26 - 27, 2010
Costa Mesa CA UNITED STATES
Read more... -
The EU Clinical Trial Directive
April 26 - 27, 2010
Berlin GERMANY
Read more... -
How to Implement Risk Management Principles and Activities within a Quality Management System
April 26 - 27, 2010
Costa Mesa CA UNITED STATES
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FDA Inspections of Clinical Data Systems
April 26 - 27, 2010
Dublin IRELAND
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Potency determination of drugs and biologics: design, and development of reliable potency bioassays
April 27, 2010
Palo Alto CA UNITED STATES
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European Filing & Registration Procedures
April 28 - 29, 2010
Berlin GERMANY
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Dermatological Product Development
April 28 - 29, 2010
Malvern PA UNITED STATES
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Free Webinar: Reaction Progress Kinetic Analysis: A Powerful Methodology For Streamlining The Study Of Complex Organic Reactions
April 28, 2010
UNITED STATES
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Essentials of Program, Project & Portfolio Management in Bio/Pharmaceutical Discovery
April 28 - 29, 2010
Malvern PA UNITED STATES
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Evolving Regulatory expectation for Particulates in Biologics
April 29, 2010
Palo Alto CA UNITED STATES
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May 2010 [+] (31 total)
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
May 3 - 5, 2010
Costa Mesa CA UNITED STATES
Read more... -
BIO International Convention 2010
May 3 - 6, 2010
Chicago IL UNITED STATES
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Latin America - Understanding Regulatory Compliance Requirements
May 4 - 5, 2010
Malvern PA UNITED STATES
Read more... -
Software Development for Medical Device Professionals
May 4 - 5, 2010
Malvern PA UNITED STATES
Read more... -
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
May 6 - 7, 2010
Costa Mesa CA UNITED STATES
Read more... -
Japan - Regulatory Filing and Compliance Processes for Life Sciences
May 6 - 7, 2010
Malvern PA UNITED STATES
Read more... -
Effective Laboratory Safety Management
May 6 - 7, 2010
Malvern PA UNITED STATES
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Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
May 10 - 11, 2010
Costa Mesa CA UNITED STATES
Read more... -
Good Laboratory Practices (GLP) for Pre-Clinical Testing
May 10 - 11, 2010
Costa Mesa CA UNITED STATES
Read more... -
Best Practices for an Effective Cleaning Validation Program
May 11 - 12, 2010
Costa Mesa CA UNITED STATES
Read more... -
Free Webinar: Faster, Better Organic Chemistry Through The Use Of Real-Time In Situ FTIR Technology & Software Optimized For The Organic Chemist
May 12, 2010
UNITED STATES
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Good Manufacturing Practices
May 12 - 14, 2010
Costa Mesa CA UNITED STATES
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Detecting Fraud and Misconduct in Clinical Trials
May 13 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
Improving Lyophilization Manufacturing and Development with ContoLyoTM Nucleation On-Demand Technology
May 13, 2010
UNITED STATES
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Process Validation for Drugs and Biologics
May 13 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
May 17 - 18, 2010
Costa Mesa CA UNITED STATES
Read more... -
Pharmaceutical Water Systems: Contemporary Technology & Compliance
May 17 - 18, 2010
Costa Mesa CA UNITED STATES
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Practical Methods for Project Management
May 17 - 18, 2010
Berlin GERMANY
Read more... -
Good Monitoring Practices for Medical Devices
May 18 - 19, 2010
Malvern PA UNITED STATES
Read more... -
Do your compendial methods comply with USP <1226>?
May 18, 2010
Palo Alto CA UNITED STATES
Read more... -
Auditing and Qualifying Suppliers and Vendors
May 19 - 20, 2010
Costa Mesa CA UNITED STATES
Read more... -
Root Cause Analysis for CAPA
May 19 - 21, 2010
Berlin GERMANY
Read more... -
Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
May 20 - 21, 2010
Malvern PA UNITED STATES
Read more... -
SBS Symposium: Biopharmaceuticals: Exploring Synergies Across Drug Formats
May 20 - 21, 2010
San Francisco CA UNITED STATES
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Writing in the Regulated Environment when English is your Second Languate
May 20 - 21, 2010
Costa Mesa CA UNITED STATES
Read more... -
ADME, PK/TK, and Drug Metabolissm in Drug Discovery and Development
May 24 - 26, 2010
Costa Mesa CA UNITED STATES
Read more... -
Tablets & Capsules - Development, Manufacture and Testing of Solid Oral Dosage Forms
May 24 - 26, 2010
Malvern PA UNITED STATES
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Clinical Trial Design for Medical Devices
May 24 - 25, 2010
Berlin GERMANY
Read more... -
Overview of FDA Regulatory Compliance for Medical Devices
May 24 - 25, 2010
Berlin GERMANY
Read more... -
Process Validation for Medical Devices
May 26 - 28, 2010
Berlin GERMANY
Read more... -
Introduction to the VirTis Encore Control System
May 27, 2010
UNITED STATES
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June 2010 [+] (24 total)
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
June 2 - 4, 2010
Costa Mesa CA UNITED STATES
Read more... -
Practical Methods for Project Management
June 3 - 4, 2010
King of Prussia PA UNITED STATES
Read more... -
Good Clinical Practices (GCP)
June 7 - 9, 2010
Costa Mesa CA UNITED STATES
Read more... -
QA/QC Strategy for Biopharmaceuticals and Biologics
June 7 - 9, 2010
Costa Mesa CA UNITED STATES
Read more... -
Reporting Failure Investigations and Process Deviations
June 9 - 11, 2010
King of Prussia PA UNITED STATES
Read more... -
11th Annual Drug Discovery Leaders Summit
June 9 - 10, 2010
Montreux SWITZERLAND
Read more... -
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
June 10 - 11, 2010
Costa Mesa CA UNITED STATES
Read more... -
Adverse Drug Events - Reporting & Regulatory Requirements
June 10 - 11, 2010
Costa Mesa CA UNITED STATES
Read more... -
Detecting Fraud and Misconduct in Clinical Trials
June 10 - 11, 2010
King of Prussia PA UNITED STATES
Read more... -
13th International Conference on Drug-Drug Interactions
June 14 - 16, 2010
Seattle WA UNITED STATES
Read more... -
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
June 14 - 16, 2010
Costa Mesa CA UNITED STATES
Read more... -
Overview of FDA Regulatory Compliance for Medical Devices
June 14 - 15, 2010
King of Prussia PA UNITED STATES
Read more... -
FDA Inspections of Clinical Data Systems
June 14 - 15, 2010
Costa Mesa CA UNITED STATES
Read more... -
Preparing the CMC Section for NDAs/CTDs/INDs
June 14 - 15, 2010
King of Prussia PA UNITED STATES
Read more... -
How to Prepare for a Systems-based Inspection - Understanding FDA's Risk-Based Inspections Approach
June 16 - 17, 2010
King of Prussia PA UNITED STATES
Read more... -
Effective Risk-Based Applications of Drug cGMPs and Validation Requirements for Cosmetics and OTC Drug Products
June 17 - 18, 2010
King of Prussia PA UNITED STATES
Read more... -
8th International Conference on Early Toxicity Scrteening
June 17 - 18, 2010
Seattle WA UNITED STATES
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
June 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Project Management for Phase 1 & 2 Clinical Trials
June 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
The Drug Development Process - From Discovery to Commercialization
June 23 - 25, 2010
King of Prussia PA UNITED STATES
Read more... -
Stability Programs for Product Shelf Life - From Development to Approval
June 24 - 25, 2010
Costa Mesa CA UNITED STATES
Read more... -
The VirTis Encore Control System for Advanced Users
June 24, 2010
UNITED STATES
Read more... -
Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
June 24 - 25, 2010
Costa Mesa CA UNITED STATES
Read more... -
Quality System Regulation for the Medical Device & Biotech Industries
June 28 - 29, 2010
Costa Mesa CA UNITED STATES
Read more...
July 2010 [+] (12 total)
-
Introduction to Effective Medical Writing
July 12 - 13, 2010
Costa Mesa CA UNITED STATES
Read more... -
Biostatistics for Non-Statisticians
July 12 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
Validation of Computer Systems
July 12 - 13, 2010
King of Prussia PA UNITED STATES
Read more... -
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 12 - 13, 2010
King of Prussia PA UNITED STATES
Read more... -
Freeze Drying of Co-Solvent Systems: Rationale, Opportunities and Applications
July 13, 2010
UNITED STATES
Read more... -
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
July 15 - 16, 2010
Costa Mesa CA UNITED STATES
Read more... -
Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
July 19 - 21, 2010
King of Prussia PA UNITED STATES
Read more... -
Design Control for Medical Device Professionals
July 20 - 21, 2010
Costa Mesa CA UNITED STATES
Read more... -
Design Validation, Verification, and Risk Analysis for Medical Device professionals
July 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
How to Monitor Clinical Trials for GCP Compliance
July 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Cleanroom Microbiology for the Non-Microbiologist
July 27 - 28, 2010
Costa Mesa CA UNITED STATES
Read more... -
Sterilization Procedures: Technology
July 29 - 30, 2010
Costa Mesa CA UNITED STATES
Read more...
August 2010 [+] (17 total)
-
Selecting and Managing CRO's
August 3 - 4, 2010
Costa Mesa CA UNITED STATES
Read more... -
Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
August 5 - 6, 2010
Costa Mesa CA UNITED STATES
Read more... -
How to Develop an Effective Complaint Handling, and Post Market Surveillance Program for Drugs & Devices
August 9 - 10, 2010
Costa Mesa CA UNITED STATES
Read more... -
Latin America - Understanding Regulatory Compliance Requirements
August 9 - 10, 2010
Costa Mesa CA UNITED STATES
Read more... -
Root Cause Analysis for CAPA
August 11 - 13, 2010
Costa Mesa CA UNITED STATES
Read more... -
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
August 11 - 12, 2010
Costa Mesa CA UNITED STATES
Read more... -
FDA Inspections - What to Expect and How to Prepare
August 16 - 17, 2010
Costa Mesa CA UNITED STATES
Read more... -
Adverse Drug Events - Reporting & Regulatory Requirements
August 16 - 17, 2010
Costa Mesa CA UNITED STATES
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
August 16 - 17, 2010
King of Prussia PA UNITED STATES
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
August 18 - 19, 2010
Costa Mesa CA UNITED STATES
Read more... -
The Drug Development Process - From Discovery to Commercialization
August 18 - 20, 2010
Costa Mesa CA UNITED STATES
Read more... -
Writing in the Regulated Environment when English is your Second Language
August 19 - 20, 2010
King of Prussia PA UNITED STATES
Read more... -
Good Clinical Practice for Medical Device Investigations
August 23 - 24, 2010
Costa Mesa CA UNITED STATES
Read more... -
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
August 23 - 25, 2010
King of Prussia CA UNITED STATES
Read more... -
Good Clinical Practice Auditing
August 25 - 26, 2010
Costa Mesa CA UNITED STATES
Read more... -
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
August 26 - 27, 2010
King of Prussia PA UNITED STATES
Read more... -
Detecting Fraud and Misconduct in Clinical Trials
August 30 - 31, 2010
Costa Mesa CA UNITED STATES
Read more...
September 2010 [+] (29 total)
-
Introduction to Molecular Biology Techniques
September 8 - 10, 2010
King of Prussia CA UNITED STATES
Read more... -
Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
September 8 - 10, 2010
Costa Mesa CA UNITED STATES
Read more... -
Preparing the CMC Section for NDAs/CTDs/INDs
September 9 - 10, 2010
Costa Mesa CA UNITED STATES
Read more... -
Root Cause Analysis for CAPA
September 13 - 15, 2010
Berlin GERMANY
Read more... -
Good Monitoring Practices for Medical Devices
September 13 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
September 14 - 15, 2010
King of Prussia PA UNITED STATES
Read more... -
Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
September 15 - 16, 2010
King of Prussia PA UNITED STATES
Read more... -
Medical Devices - EU Directives, CE Marking and ISO Standard Certifications
September 15 - 16, 2010
Costa Mesa CA UNITED STATES
Read more... -
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 15 - 17, 2010
King of Prussia PA UNITED STATES
Read more... -
Stability Programs for Product Shelf Life - From Development to Approval
September 16 - 17, 2010
King of Prussia PA UNITED STATES
Read more... -
Analytical Method Validation for Biologics, Biopharmaceticals and Other Therapeutic Products
September 16 - 17, 2010
Dublin IRELAND
Read more... -
Pharmaceutical Production Batch Record Review
September 16 - 17, 2010
Berlin GERMANY
Read more... -
Labeling and Labeling Controls for Medical Devices
September 20 - 21, 2010
Costa Mesa CA UNITED STATES
Read more... -
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
September 20 - 22, 2010
Dublin IRELAND
Read more... -
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
September 20 - 22, 2010
King of Prussia PA UNITED STATES
Read more... -
Validation of Computer Systems
September 20 - 21, 2010
Dublin IRELAND
Read more... -
Software Development for Medical Device Professionals
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Purchasing Controls in the Medical Device Industry
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Design Control for Medical Device Professionals
September 27 - 28, 2010
Dublin IRELAND
Read more... -
Good Laboratory Practices for Pre-Clinical Testing
September 27 - 28, 2010
King of Prussia PA UNITED STATES
Read more... -
Best Practices for an Effective Cleaning Validation Program
September 27 - 28, 2010
King of Prussia PA UNITED STATES
Read more... -
Adverse Drug Events - Reporting & Regulatory Requirements
September 27 - 28, 2010
Dublin IRELAND
Read more... -
The EU Clinical Trial Directive
September 28 - 29, 2010
King of Prussia PA UNITED STATES
Read more... -
Good Manufacturing Practices
September 29, 2010 - October 1, 2010
King of Prussia PA UNITED STATES
Read more... -
The Drug Development Process - From Discovery to Commercialization
September 29, 2010 - October 1, 2010
Dublin IRELAND
Read more... -
Design Validation, Verification, and Risk Analysis for Medical Device professionals
September 29 - 30, 2010
Dublin IRELAND
Read more... -
Process Validation for Drugs and Biologics
September 29 - 30, 2010
King of Prussia PA UNITED STATES
Read more... -
European Filing & Registration Procedures
September 30, 2010 - October 1, 2010
King of Prussia PA UNITED STATES
Read more... -
3rd International Symposium on Green Processing in the Pharmaceutical & Fine Chemical Industries
September 30, 2010 - October 1, 2010
Boston MA UNITED STATES
Read more...
October 2010 [+] (0 total)
November 2010 [+] (0 total)
December 2010 [+] (0 total)
January 2011 [+] (0 total)
February 2011 [+] (0 total)
March 2011 [+] (0 total)
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