Events Calendar
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Events By Name
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Upcoming Events
- September 7, 2010 - ComplianceOnline Webinar - How to conduct a software risk assessment that is meaningful
- September 8, 2010 - ComplianceOnline Webinar - How do I keep FDA happy with my contract manufacturer?
- September 8, 2010 - ComplianceOnline Webinar - Engineering and Laboratory Mythology with Water System
- September 8 - 10, 2010 - Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
- September 8 - 10, 2010 - Introduction to Molecular Biology Techniques
Events By Month
Click on a month below to view its associated events.
September 2010 [+] (58 total)
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ComplianceOnline Webinar - Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
September 1, 2010
Palo Alto CA UNITED STATES
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Full day Virtual Seminar - Effective Computer System Validation and software implementation to reduce cost and time
September 1, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Vendor selection in clinical trials, assessment activities, audits and log of preferred partners
September 2, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - How to conduct a software risk assessment that is meaningful
September 7, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - How do I keep FDA happy with my contract manufacturer?
September 8, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Engineering and Laboratory Mythology with Water System
September 8, 2010
Palo Alto CA UNITED STATES
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Introduction to Molecular Biology Techniques
September 8 - 10, 2010
King of Prussia CA UNITED STATES
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Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
September 8 - 10, 2010
Costa Mesa CA UNITED STATES
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Controlling Change to meet GMP Requirements
September 9, 2010
Palo Alto CA UNITED STATES
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Preparing the CMC Section for NDAs/CTDs/INDs
September 9 - 10, 2010
Costa Mesa CA UNITED STATES
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ComplianceOnline Webinar -Developing Supplier Quality Auditor Training Programs
September 9, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Key Factors to Write an Effective Standard Operating Procedure (SOP)
September 9, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Configuring Your System for Lean Documents
September 10, 2010
Palo Alto CA UNITED STATES
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Root Cause Analysis for CAPA
September 13 - 15, 2010
Berlin GERMANY
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Good Monitoring Practices for Medical Devices
September 13 - 14, 2010
Costa Mesa CA UNITED STATES
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ComplianceOnline Webinar - The role of Analytical Program to Support Drug Development Process
September 14, 2010
Palo Alto CA UNITED STATES
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Developing an ethylene oxide (EO) sterilization process for a product with limitations
September 14, 2010
Palo Alto CA UNITED STATES
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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
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Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
September 15 - 16, 2010
King of Prussia PA UNITED STATES
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ComplianceOnline Virtual Seminar - Effective Corrective and Preventive Actions (CAPA): 10 Steps to Success
September 15, 2010
Palo Alto CA UNITED STATES
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Medical Devices - EU Directives, CE Marking and ISO Standard Certifications
September 15 - 16, 2010
Costa Mesa CA UNITED STATES
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 15 - 17, 2010
King of Prussia PA UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
September 16 - 17, 2010
King of Prussia PA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceticals and Other Therapeutic Products
September 16 - 17, 2010
Dublin IRELAND
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ComplianceOnline Webinar - Navigating Pediatric Trials from recruitment to successful on-time completion
September 16, 2010
Palo Alto CA UNITED STATES
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Medical Devices in the EU: CE Mark and 93/42/EEC Directive
September 16, 2010
Palo Alto CA UNITED STATES
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Pharmaceutical Production Batch Record Review
September 16 - 17, 2010
Berlin GERMANY
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The Pan African Health Expo and Conference 2010
September 16 - 18, 2010
Johannesburg AL SOUTH AFRICA
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ComplianceOnline Webinar - Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
September 17, 2010
Palo Alto CA UNITED STATES
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Labeling and Labeling Controls for Medical Devices
September 20 - 21, 2010
Costa Mesa CA UNITED STATES
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8th Annual Cold Chain Distribution for Pharmaceuticals Global Forum
September 20 - 23, 2010
Philadelphia PA UNITED STATES
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
September 20 - 22, 2010
Dublin IRELAND
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
September 20 - 22, 2010
King of Prussia PA UNITED STATES
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Validation of Computer Systems
September 20 - 21, 2010
Dublin IRELAND
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ComplianceOnline Webinar - What are the “Good Clinical Practices” (GCP) of Research involving Human Subjects
September 21, 2010
Palo Alto CA UNITED STATES
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Medical Device Changes and The 510(k)
September 21, 2010
Palo Alto CA UNITED STATES
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Purchasing Controls in the Medical Device Industry
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
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ComplianceOnline Webinar - The ICF Process: Tips on Achieving Optimal compliance and Comprehension
September 22, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Stability Program to support Shipping and Distribution of Drug Products
September 22, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - The Hero of Manufacturing Contamination Control -- The Microbiology Lab
September 22, 2010
Palo Alto CA UNITED STATES
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Software Development for Medical Device Professionals
September 22 - 23, 2010
Costa Mesa CA UNITED STATES
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ComplianceOnline Webinar - Laboratory Investigation Out-of-Specification Results
September 23, 2010
Palo Alto CA UNITED STATES
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CAPA for Manufacturing, Financial Service Companies: Get it Right the First Time (Efficient Process)
September 23, 2010
Palo Alto CA UNITED STATES
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Good Laboratory Practices for Pre-Clinical Testing
September 27 - 28, 2010
King of Prussia PA UNITED STATES
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Best Practices for an Effective Cleaning Validation Program
September 27 - 28, 2010
King of Prussia PA UNITED STATES
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Adverse Drug Events - Reporting & Regulatory Requirements
September 27 - 28, 2010
Dublin IRELAND
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Design Control for Medical Device Professionals
September 27 - 28, 2010
Dublin IRELAND
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ComplianceOnline Webinar - How to Use Foreign Trial Data in Your NDA Approval Process
September 28, 2010
Palo Alto CA UNITED STATES
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Validating Radiation Sterilization for medical device industries
September 28, 2010
Palo Alto CA UNITED STATES
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The EU Clinical Trial Directive
September 28 - 29, 2010
King of Prussia PA UNITED STATES
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Good Manufacturing Practices
September 29, 2010 - October 1, 2010
King of Prussia PA UNITED STATES
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The Drug Development Process - From Discovery to Commercialization
September 29, 2010 - October 1, 2010
Dublin IRELAND
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Design Validation, Verification, and Risk Analysis for Medical Device professionals
September 29 - 30, 2010
Dublin IRELAND
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Process Validation for Drugs and Biologics
September 29 - 30, 2010
King of Prussia PA UNITED STATES
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ComplianceOnline Webinar - Ensuring GCP compliance through quality auditing in clinical trial
September 29, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Critical Role of Quality Audit in GxP Compliance & Improvement
September 29, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
September 30, 2010
Palo Alto CA UNITED STATES
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European Filing & Registration Procedures
September 30, 2010 - October 1, 2010
King of Prussia PA UNITED STATES
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October 2010 [+] (38 total)
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ComplianceOnline Webinar - GMPs in Biopharmaceutical Development Laboratories
October 1, 2010
Palo Alto CA UNITED STATES
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Practical Methods for Project Management
October 4 - 5, 2010
King of Prussia PA UNITED STATES
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Patent and Other Intellectual Property Law for the Life Sciences Industry
October 4 - 5, 2010
King of Prussia PA UNITED STATES
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Tablets & Capsules - Development, Manufacture and Testing of Solid Oral Dosage Forms
October 4 - 6, 2010
Costa Mesa CA UNITED STATES
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Validation of Computer Systems
October 4 - 5, 2010
Costa Mesa CA UNITED STATES
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ComplianceOnline Webinar - The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
October 5, 2010
Palo Alto CA UNITED STATES
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Effective Quality Assurance Auditing for FDA Regulated Industries
October 5 - 6, 2010
King of Prussia PA UNITED STATES
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The EU Clinical Trial Directive
October 5 - 6, 2010
Dublin IRELAND
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ComplianceOnline Webinar - Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections
October 7, 2010
Palo Alto CA UNITED STATES
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
October 7 - 8, 2010
King of Prussia PA UNITED STATES
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European Filing & Registration Procedures
October 7 - 8, 2010
Dublin IRELAND
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How to Implement Risk Management Principles and Activities within a Quality Management System
October 7 - 8, 2010
King of Prussia PA UNITED STATES
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Quality System Regulation for the Medical Device & Biotech Industries
October 7 - 8, 2010
King of Prussia PA UNITED STATES
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FDA Inspections - What to Expect and How to Prepare
October 11 - 12, 2010
King of Prussia PA UNITED STATES
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How to Monitor Clinical Trials for GCP Compliance
October 11 - 12, 2010
King of Prussia PA UNITED STATES
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Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
October 11 - 12, 2010
Dublin IRELAND
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Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
October 12 - 13, 2010
King of Prussia PA UNITED STATES
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Detecting Fraud & Misconduct in Clinical Trials
October 13 - 14, 2010
King of Prussia PA UNITED STATES
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Process Validation for Medical Devices
October 13 - 15, 2010
King of Prussia PA UNITED STATES
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QA/QC Strategy for Biopharmaceuticals and Biologics
October 13 - 15, 2010
King of Prussia PA UNITED STATES
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Pharmaceutical Production Batch Record Review
October 14 - 15, 2010
King of Prussia PA UNITED STATES
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ComplianceOnline Webinar - Preparing for and handling FDA Laboratory GMP inspections
October 15, 2010
Palo Alto CA UNITED STATES
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ComplianceOnline Webinar - Importance of Method Validation Protocols and components of MVP in the Laboratory
October 15, 2010
Palo Alto CA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
October 18 - 19, 2010
King of Prussia PA UNITED STATES
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Introduction to Statistical Analysis of Laboratory Data
October 18 - 19, 2010
King of Prussia PA UNITED STATES
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Biostatistics for Non-Statisticians
October 20 - 22, 2010
King of Prussia PA UNITED STATES
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
October 20 - 22, 2010
King of Prussia PA UNITED STATES
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Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137
October 20, 2010
Palo Alto CA UNITED STATES
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Auditing and Qualifying Suppliers and Vendors
October 21 - 22, 2010
Berlin GERMANY
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Essentials of Program, Project & Portfolio Management in Bio/Pharmaceutical Discovery
October 21 - 22, 2010
King of Prussia PA UNITED STATES
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Best Practices for an Effective Cleaning Validation Program
October 25 - 26, 2010
Berlin GERMANY
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Design Control for Medical Device Professionals
October 25 - 26, 2010
King of Prussia PA UNITED STATES
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Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
October 25 - 26, 2010
King of Prussia PA UNITED STATES
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Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
October 26 - 27, 2010
King of Prussia PA UNITED STATES
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Design Validation, Verification, and Risk Analysis for Medical Device Professionals
October 27 - 28, 2010
King of Prussia PA UNITED STATES
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Process Validation for Drugs and Biologics
October 27 - 28, 2010
Berlin GERMANY
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FDA Inspections of Clinical Data Systems
October 28 - 29, 2010
King of Prussia PA UNITED STATES
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Introduction to Effective Medical Writing
October 28 - 29, 2010
King of Prussia PA UNITED STATES
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November 2010 [+] (22 total)
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Project Management for Phase 1 & 2 Clinical Trials
November 1 - 2, 2010
King of Prussia PA UNITED STATES
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
November 2 - 3, 2010
Berlin GERMANY
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Selecting and Managing CROs
November 2 - 3, 2010
Berlin GERMANY
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Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
November 3 - 5, 2010
King of Prussia PA UNITED STATES
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Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
November 3 - 4, 2010
King of Prussia PA UNITED STATES
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Spectroscopic Method Development for the Pharmaceutical and Biotech Industries
November 3 - 5, 2010
King of Prussia PA UNITED STATES
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Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
November 4 - 5, 2010
Berlin GERMANY
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Effective Laboratory Safety Management
November 4 - 5, 2010
King of Prussia PA UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
November 4 - 5, 2010
Berlin GERMANY
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ComplianceOnline Webinar - Excel Spreadsheets - Develop and Validate to Eliminate 483s
November 5, 2010
Palo Alto CA UNITED STATES
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Cleanroom Microbiology for the Non-Microbiologist
November 8 - 9, 2010
King of Prussia PA UNITED STATES
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
November 10 - 12, 2010
Dublin IRELAND
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The Drug Development Process - From Discovery to Commercialization
November 10 - 12, 2010
King of Prussia PA UNITED STATES
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Sterilization Procedures: Technology, Equipment & Validation
November 10 - 11, 2010
King of Prussia PA UNITED STATES
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Preparing the CMC Section for the NDAs/CTDs/INDs
November 11 - 12, 2010
King of Prussia PA UNITED STATES
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Good Clinical Practices (GCP)
November 15 - 17, 2010
King of Prussia PA UNITED STATES
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Latin America - Understanding Regulatory Compliance Requirements
November 15 - 16, 2010
King of Prussia PA UNITED STATES
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Pharmaceutical Water Systems: Contemporary Technology & Compliance
November 16 - 17, 2010
King of Prussia PA UNITED STATES
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Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
November 17 - 18, 2010
King of Prussia PA UNITED STATES
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Effective Risk-Based Applications of Drug cGMPs and Validation Requirements for Cosmetics and OTC Products
November 18 - 19, 2010
King of Prussia PA UNITED STATES
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Selecting and Managing CROs
November 30, 2010 - December 1, 2010
King of Prussia PA UNITED STATES
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ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP <1226>
November 30, 2010
Palo Alto CA UNITED STATES
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December 2010 [+] (13 total)
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Good Manufacturing Practices
December 1 - 3, 2010
Costa Mesa CA UNITED STATES
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Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
December 1 - 3, 2010
King of Prussia PA UNITED STATES
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Clinical Trial Design for Medical Devices
December 2 - 3, 2010
Costa Mesa CA UNITED STATES
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Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
December 2 - 3, 2010
King of Prussia PA UNITED STATES
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
December 2 - 3, 2010
Costa Mesa CA UNITED STATES
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
December 6 - 8, 2010
King of Prussia PA UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
December 6 - 7, 2010
Costa Mesa CA UNITED STATES
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Root Cause Analysis for CAPA
December 8 - 10, 2010
King of Prussia PA UNITED STATES
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Software Development for Medical Device Professionals
December 8 - 9, 2010
King of Prussia PA UNITED STATES
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
December 8 - 10, 2010
Costa Mesa CA UNITED STATES
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Good Clinical Practice for Medical Device Investigations
December 13 - 14, 2010
King of Prussia PA UNITED STATES
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Overview of FDA Regulatory Compliance for Medical Devices
December 13 - 14, 2010
King of Prussia PA UNITED STATES
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Good Clinical Practice Auditing
December 15 - 16, 2010
King of Prussia PA UNITED STATES
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