Events Calendar
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Events By Name
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Upcoming Events
- May 20 - 21, 2012 - 4th Biennial Emirates Physiotherapy Conference 2012
- May 21 - 22, 2012 - The EU Clinical Trial Directive
- May 21 - 22, 2012 - FDA Inspections -What Regulators Expect and How to Prepare
- May 21 - 22, 2012 - Writing Effective Standard Operating Procedures and Other Process Documents
- May 22, 2012 - Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
Events By Month
Click on a month below to view its associated events.
May 2012 [+] (40 total)
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21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits - Webinar By GlobalCompliancePanel
May 1, 2012
Online Training DE US
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Best Practices For An Effective Cleaning Validation Program
May 1 - 2, 2012
Los Angeles CA US
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Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
May 2 - 4, 2012
King of Prussia PA US
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Process Validation for Drugs and Biologics
May 3 - 4, 2012
Los Angeles CA US
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Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems - Webinar By GlobalCompliancePanel
May 3, 2012
Online Training DE US
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Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues
May 3, 2012
Palo Alto CA US
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Validation and 21 CFR Part 11 Compliance of Computer Systems - US Seminar 2012 at San Francisco
May 3 - 4, 2012
San Francisco, Marriott Marquis Downtown CA US
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Validation of Computer Systems
May 7 - 8, 2012
Berlin DE
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Proper Documentation of Risk Management for Compliance with ISO 14971 - Webinar By GlobalCompliancePanel
May 8, 2012
Online Training DE US
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FDA Software Validation Self-Check – plan an effective Internal Audit program
May 9, 2012
Palo Alto CA US
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Device Changes and the 510(k) - Webinar By GlobalCompliancePanel
May 9, 2012
Online Training DE US
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FDA Software Validation Self-Check – plan an effective Internal Audit program
May 9, 2012
Palo Alto CA US
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Process Analytical Technology (PAT) is more than it Seems - US Seminar 2012 at San Francisco
May 10 - 11, 2012
San Francisco, Marriott Marquis Downtown CA US
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Logical Water System Validation - Webinar By ComplianceOnline
May 11, 2012
Palo Alto CA US
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Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 11, 2012
Palo Alto CA US
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Logical Water System Validation - Webinar By ComplianceOnline
May 11, 2012
Palo Alto CA US
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The Drug Development Process - From Discovery to Commercialization
May 14 - 16, 2012
Los Angeles CA US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
May 15 - 16, 2012
Los Angeles CA US
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Aspects to Consider for Clean Room Qualification and Operation - Webinar By GlobalCompliancePanel
May 15, 2012
Online Training DE US
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Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
May 15, 2012
Online Training DE US
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Practical Methods for Project Management
May 16 - 17, 2012
Dublin IE
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
May 16 - 18, 2012
Los Angeles CA US
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Analytical Test Methods Validation: FDA, ICH and USP Requirements
May 17, 2012
Palo Alto CA US
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Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach
May 17 - 18, 2012
Los Angeles CA US
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HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding
May 17 - 18, 2012
Boston Marriott Long Wharf 8 AM to 5 PM EDT MA US
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4th Biennial Emirates Physiotherapy Conference 2012
May 20 - 21, 2012
Dubai AE
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The EU Clinical Trial Directive
May 21 - 22, 2012
King of Prussia PA US
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FDA Inspections -What Regulators Expect and How to Prepare
May 21 - 22, 2012
Dublin IE
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Writing Effective Standard Operating Procedures and Other Process Documents
May 21 - 22, 2012
Los Angeles CA US
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Supplier Controls to Meet Tougher U.S. FDA Requirements
May 22, 2012
Palo Alto CA US
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Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
May 22, 2012
Online Training DE US
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 23 - 24, 2012
Los Angeles CA US
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FDA Warning Letter - Consent Decree Software Validation
May 23, 2012
Palo Alto CA US
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DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
May 23, 2012
Online Training DE US
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Pre-Approval Statements and Representations by Pharmaceutical Manufacturers
May 24, 2012
Palo Alto CA US
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Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel
May 24, 2012
Online Training DE US
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Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
May 24 - 25, 2012
Courtyard by Marriott Washington, DC WA US
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European Filing and Registration Procedures
May 28 - 29, 2012
Dublin IE
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Risk-Based Validation Equipment Validation - Webinar By ComplianceOnline
May 31, 2012
Palo Alto CA US
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Risk-Based Validation Equipment Validation - Webinar By ComplianceOnline
May 31, 2012
Palo Alto CA US
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June 2012 [+] (25 total)
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Practical Methods for Project Management
June 4 - 5, 2012
King of Prussia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Drug Products
June 4 - 5, 2012
Los Angeles CA US
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Good Clinical Practices (GCPs)
June 4 - 6, 2012
Los Angeles CA US
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ICH Q10; moving from GMPs to a Pharmaceutical Quality System
June 5, 2012
Palo Alto CA US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
June 6 - 7, 2012
Los Angeles CA US
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Latin America - Understanding Regulatory Compliance Requirements
June 6 - 8, 2012
Los Angeles CA US
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Adverse Drug Events – Understanding and Reporting Requirements
June 7 - 8, 2012
Los Angeles CA US
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The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
June 11 - 12, 2012
King of Prussia PA US
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Validation of Computer Systems
June 11 - 12, 2012
Los Angeles CA US
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Global Pharma Manufacturing Summit 2012
June 11 - 12, 2012
New Jersey NJ US
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
June 11 - 12, 2012
Los Angeles CA US
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FDA Inspections -What Regulators Expect and How to Prepare
June 12 - 13, 2012
Los Angeles CA US
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FDA Warning Letter Closeout Program - Webinar By ComplianceOnline
June 12, 2012
Palo Alto CA US
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QA/QC Strategy for Biopharmaceuticals and Biologics
June 13 - 15, 2012
Los Angeles CA US
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements)and Communicating with the FDA
June 18 - 19, 2012
Los Angeles CA US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
June 19 - 20, 2012
King of Prussia PA US
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Reduce COTS Software Validation using the risk-based approach
June 19, 2012
Palo Alto CA US
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
June 20 - 22, 2012
Los Angeles CA US
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Preparing the CMC Section for NDAs-CTDs-INDs
June 25 - 26, 2012
King of Prussia PA US
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Lyophilization Technology - Practical Application of the Scientific Principles
June 25 - 27, 2012
Los Angeles CA US
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Biosimilars – Understanding the Regulatory Challenges
June 25 - 26, 2012
Los Angeles CA US
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Project Management for Phase 1 & 2 Clinical Trials
June 25 - 26, 2012
Los Angeles CA US
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Project Management for Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
June 27 - 28, 2012
Los Angeles CA US
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FDA's new enforcement initiative – Strategic Software Validation Planning for Executives and Managers
June 27, 2012
Palo Alto CA US
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Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems
June 28, 2012
Palo Alto CA US
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July 2012 [+] (16 total)
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Introduction to Effective Medical Writing
July 9 - 10, 2012
Los Angeles CA US
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Biostatistics for Non-Statisticians
July 9 - 11, 2012
Los Angeles CA US
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GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters
July 11, 2012
Palo Alto CA US
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GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters
July 11, 2012
Palo Alto CA US
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Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
July 11 - 13, 2012
Los Angeles CA US
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 16 - 17, 2012
King of Prussia PA US
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Pharmaceutical Production Batch Record Review
July 16 - 17, 2012
King of Prussia PA US
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Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
July 16 - 17, 2012
King of Prussia PA US
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Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
July 19 - 20, 2012
King of Prussia PA US
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How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
July 23 - 24, 2012
Los Angeles CA US
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Protein Expression Technologies from E. colit to Mammalian
July 23 - 25, 2012
King of Prussia PA US
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European Filing and Registration Procedures
July 23 - 24, 2012
King of Prussia PA US
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Medical Devices – Field Actions and Their Management - Recalls, Product Recovery and Safety Alerts
July 23 - 24, 2012
King of Prussia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
July 24 - 25, 2012
Los Angeles CA US
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Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
July 25, 2012
Palo Alto CA US
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GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
July 30 - 31, 2012
Los Angeles CA US
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August 2012 [+] (12 total)
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Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
August 2 - 3, 2012
King of Prussia PA US
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Good Laboratory Practices for Pre-Clinical Testing
August 6 - 7, 2012
Los Angeles CA US
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Active Pharmaceutical Ingredient (API) and Drug Product Specifications
August 6 - 8, 2012
Los Angeles CA US
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Spreadsheet Validation: Understanding and satisfying FDA requirements
August 8, 2012
Palo Alto CA US
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Good Manufacturing Practices
August 8 - 10, 2012
Los Angeles CA US
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Spreadsheet Validation: Understanding and satisfying FDA requirements
August 8, 2012
Palo Alto CA US
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Stability Programs for Product Shelf Life - From Development to Approval
August 9 - 10, 2012
Los Angeles CA US
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The Drug Development Process - From Discovery to Commercialization
August 15 - 17, 2012
King of Prussia PA US
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The 6 Most Common Problems in FDA Software Validation & Verification
August 22, 2012
Palo Alto CA US
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The 6 Most Common Problems in FDA Software Validation & Verification
August 22, 2012
Palo Alto CA US
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
August 27 - 29, 2012
Los Angeles CA US
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Pharmaceutical, Biopharmaceutical, and Biologics Quality Control Laboratories: A Regulatory Compliance Primer
August 30 - 31, 2012
Los Angeles CA US
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September 2012 [+] (15 total)
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Validation and use of Excel spreadsheets in FDA regulated environments
September 5, 2012
Palo Alto CA US
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Validation and use of Excel spreadsheets in FDA regulated environments
September 5, 2012
Palo Alto CA US
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How to Implement Risk Management Principles and Activities Within A Quality Management System
September 10 - 11, 2012
King of Prussia PA US
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Clinical Document Management - A Trial by Trial Approach to Compliance
September 10 - 11, 2012
King of Prussia PA US
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Design Control for Medical Device Professionals
September 10 - 11, 2012
Berlin DE
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Process Validation for Medical Devices
September 12 - 14, 2012
King of Prussia PA US
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Selecting and Managing CROs
September 12 - 13, 2012
King of Prussia PA US
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 12 - 14, 2012
King of Prussia PA US
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Design Validation, Verification, and Risk Analysis for Medical Device Professionals
September 12 - 13, 2012
Berlin DE
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The EU Clinical Trial Directive
September 17 - 18, 2012
Dublin IE
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 17 - 19, 2012
Dublin IE
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Risk Assessment-Compliance Using Easy To Fill Out Documentation
September 18, 2012
Palo Alto CA US
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Best Practices For An Effective Cleaning Validation Program
September 18 - 19, 2012
King of Prussia PA US
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Introduction to Medical Combination Products
September 18 - 19, 2012
King of Prussia PA US
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Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions
September 20 - 21, 2012
King of Prussia PA US
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October 2012 [+] (1 total)
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UAE Cancer Congress
October 11 - 13, 2012
Dubai AE
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