Events Calendar
Welcome to the Medical Design Online Events Calendar!
Use this page to view Upcoming Events, jump to Advanced Search, or begin to Post Events.
Events By Name
Enter the event name in the form below and click on the search button to obtain event information. For a more powerful search with additional filters, try our Advanced Search.
Upcoming Events
- March 24, 2010 - Overview of the Medical Device Risk Management Standard-ISO 14971
- March 24, 2010 - Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe
- March 24 - 26, 2010 - Root Cause Analysis for CAPA
- March 24 - 26, 2010 - Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
- March 24 - 25, 2010 - Project Management for Phast 3 & LCM (Life Cycle Management) of the Drug Development Process
Events By Month
Click on a month below to view its associated events.
March 2010 [+] (52 total)
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Adverse Drug Events - Reporting & Regulatory Requirements
March 1 - 2, 2010
Berlin GERMANY
Read more... -
Good Clinical Practice for Medical Device Investigations
March 1 - 2, 2010
Malvern PA UNITED STATES
Read more... -
Biostatistics for Non-Statisticians
March 1 - 3, 2010
Berlin GERMANY
Read more... -
Setting Up and Running a Tougher Supplier Audit Program
March 2, 2010
Online Webinar 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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Business, Project and Compliance Risk
March 2, 2010
Online Webinar DE UNITED STATES
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Business, Project and Compliance Risk
March 2, 2010
Online Webinar DE UNITED STATES
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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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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 Compliant HPLC Qualification and Performance Testing
March 4, 2010
Online Webinar DE UNITED STATES
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The 510(k) Submission: Requirements, Contents, and Options
March 4, 2010
Online Webinar DE UNITED STATES
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The 510(k) Submission: Requirements, Contents, and Options
March 4, 2010
Online Webinar DE UNITED STATES
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21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection
March 4, 2010
Online Webinar DE UNITED STATES
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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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Foreign Material Control
March 9, 2010
Online Webinar DE UNITED STATES
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Validating Radiation Sterilization for medical device industries
March 9, 2010
Online Webinar DE 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
Read more... -
The CTD/eCTD: Building the Marketing Application throughout Clinical Development
March 10 - 12, 2010
Malvern PA UNITED STATES
Read more... -
Excel Spreadsheet Validation To Eliminate 483s
March 10, 2010
Online Webinar DE UNITED STATES
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Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems
March 11, 2010
Online Webinar DE UNITED STATES
Read more... -
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
Read more... -
Preparing the CMC Section for NDAs/CTDs/INDs
March 15 - 16, 2010
Costa Mesa CA UNITED STATES
Read more... -
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
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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
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How to implement parametric release in EO sterilization-Practical approach
March 18, 2010
Palo Alto CA UNITED STATES
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Validating Radiation Sterilization for medical device industries
March 19, 2010
Palo Alto CA UNITED STATES
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Overview of FDA Regulatory Compliance for Medical Devices
March 22 - 23, 2010
Dublin IRELAND
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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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What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained
March 22, 2010
Palo Alto CA UNITED STATES
Read more... -
Root Cause Analysis for CAPA
March 24 - 26, 2010
Dublin IRELAND
Read more... -
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
Read more... -
Overview of the Medical Device Risk Management Standard-ISO 14971
March 24, 2010
Palo Alto CA UNITED STATES
Read more... -
Clinical Evaluation Reports (CER's) Required for All Classes of Medical Devices in Europe
March 24, 2010
Palo Alto CA UNITED STATES
Read more... -
Regulatory Requirements for Medical Device Calibration Programs
March 26, 2010
Palo Alto CA UNITED STATES
Read more... -
Effective Quality Assurance Auditing for FDA Regulated Industries
March 29 - 30, 2010
Dublin IRELAND
Read more... -
Selecting and Managing CROs
March 29 - 30, 2010
Malvern PA UNITED STATES
Read more... -
ISO 13485:2003 for Medical Devices - How it differs to ISO 9001:2008 and FDA part 820 requirements
March 31, 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
Read more...
April 2010 [+] (36 total)
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Requirements of validation and control of EO Sterilization
April 6, 2010
Palo Alto CA UNITED STATES
Read more... -
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
Read more... -
Quality System Regulation for the Medical Device & Biotech Industries
April 8 - 9, 2010
King of Prussia PA UNITED STATES
Read more... -
ISO 14971:2007 and the CE-Mark
April 9, 2010
Palo Alto CA UNITED STATES
Read more... -
Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
April 12 - 13, 2010
Dublin IRELAND
Read more... -
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... -
Reducing Ethylene Oxide (EO) Sterilization costs while maintaining regulatory compliance
April 14, 2010
Palo Alto CA UNITED STATES
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Writing Effective Standard Operating Procedures and Other Process Documents
April 15 - 16, 2010
Berlin GERMANY
Read more... -
Patent and Other Intellectual Property Law for the Life Sciences Industry
April 15 - 16, 2010
Costa Mesa CA UNITED STATES
Read more... -
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
Read more... -
Understanding International Standards for Medical Devices
April 20, 2010
Palo Alto CA UNITED STATES
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Process Validation for Medical Devices
April 21 - 23, 2010
Costa Mesa CA UNITED STATES
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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... -
Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
April 22 - 23, 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
Read more... -
FDA Inspections of Clinical Data Systems
April 26 - 27, 2010
Dublin IRELAND
Read more... -
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... -
Essentials of Program, Project & Portfolio Management in Bio/Pharmaceutical Discovery
April 28 - 29, 2010
Malvern PA UNITED STATES
Read more... -
European Filing & Registration Procedures
April 28 - 29, 2010
Berlin GERMANY
Read more... -
Dermatological Product Development
April 28 - 29, 2010
Malvern PA UNITED STATES
Read more... -
The FDA’s New Emphasis on Supplier Controls? Is Your Company Ready?
April 29, 2010
Palo Alto CA UNITED STATES
Read more...
May 2010 [+] (25 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... -
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... -
Effective Laboratory Safety Management
May 6 - 7, 2010
Malvern PA UNITED STATES
Read more... -
Japan - Regulatory Filing and Compliance Processes for Life Sciences
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... -
Good Manufacturing Practices
May 12 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
Detecting Fraud and Misconduct in Clinical Trials
May 13 - 14, 2010
Costa Mesa CA UNITED STATES
Read more... -
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
Read more... -
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... -
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... -
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
Read more... -
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...
June 2010 [+] (20 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... -
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... -
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
June 10 - 11, 2010
Costa Mesa CA 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... -
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... -
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... -
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... -
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... -
Stability Programs for Product Shelf Life - From Development to Approval
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 [+] (11 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... -
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)
-
Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
September 8 - 10, 2010
Costa Mesa CA UNITED STATES
Read more... -
Introduction to Molecular Biology Techniques
September 8 - 10, 2010
King of Prussia 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... -
The Pan African Health Expo and Conference 2010
September 16 - 18, 2010
Johannesburg AL SOUTH AFRICA
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... -
Purchasing Controls in the Medical Device Industry
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
Read more... -
Software Development for Medical Device Professionals
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
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... -
Design Control for Medical Device Professionals
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...
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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