Events Calendar
Upcoming Events
- May 20 - 22, 2013 - Understanding GMP Expectations for PET Drug Production
- May 21, 2013 - Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
- May 22, 2013 - Trial Master File (TMF): FDA Expectations from Sponsors and Sites
- May 22, 2013 - Trial Master File (TMF): FDA Expectations from Sponsors and Sites
- May 22, 2013 - Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Events By Month
Click on a month below to view its associated events.
May 2013 [+] (23 total)
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
May 1 - 3, 2013
Los Angeles CA US
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Process Validation for Medical Devices
May 6 - 8, 2013
Los Angeles CA US
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The Drug Development Process - From Discovery to Commercialization
May 6 - 8, 2013
Los Angeles CA US
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Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality
May 7, 2013
san Francisco CA US
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Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality
May 7, 2013
san Francisco CA US
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7th Drug Design and Medicinal Chemistry Conference
May 8 - 9, 2013
Boston MA US
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The EU Clinical Trial Directive
May 9 - 10, 2013
Los Angeles CA US
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 9 - 10, 2013
King of Prussia PA US
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Pediatric Clinical Trial Design
May 13 - 14, 2013
Berlin DE
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Good Manufacturing Practices
May 13 - 15, 2013
Berlin DE
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Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
May 13 - 15, 2013
Los Angeles CA US
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2013 PDA/FDA Container Closure Components and Systems Workshop
May 14 - 15, 2013
Bethesda MD US
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Clinical Trial Design for Medical Devices
May 15 - 16, 2013
Berlin DE
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Effective Risk-Based Applications of Drug cGMPs and Validation Requirements of Cosmetics and OTC Drug Products
May 15 - 16, 2013
Berlin DE
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Writing Effective Standard Operating Procedures and Other Process Documents
May 16 - 17, 2013
Los Angeles CA US
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Understanding GMP Expectations for PET Drug Production
May 20 - 22, 2013
Los Angeles CA US
Read more... -
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
May 21, 2013
san francisco CA US
Read more... -
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
May 22, 2013
san francisco CA US
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Trial Master File (TMF): FDA Expectations from Sponsors and Sites
May 22, 2013
san Francisco CA US
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Trial Master File (TMF): FDA Expectations from Sponsors and Sites
May 22, 2013
san Francisco CA US
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BioSeparation Forum
May 29, 2013
Leiden NL
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Princeton Supply Chain Workshop
May 30, 2013
Princeton NJ US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
May 30 - 31, 2013
Berlin DE
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June 2013 [+] (20 total)
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Adverse Drug Events – Understanding and Reporting Requirements
June 3 - 4, 2013
Los Angeles CA US
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2013 PDA/FDA Supply Chain Workshop
June 3 - 5, 2013
Bethesda, MD MD US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
June 5 - 6, 2013
Los Angeles CA US
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Good Clinical Practices (GCP) – Understanding and Implementing the Current Global Requirements
June 5 - 7, 2013
King of Prussia PA US
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Auditing and Qualifying Suppliers and Vendors
June 6 - 7, 2013
Los Angeles CA US
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Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
June 10 - 11, 2013
Berlin DE
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Validation of Computer Systems
June 10 - 11, 2013
Los Angeles CA US
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Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
June 10 - 12, 2013
Los Angeles CA US
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Biosimilars – Understanding the Regulatory Challenges
June 13 - 14, 2013
Los Angeles CA US
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Best Practices For An Effective Cleaning Validation Program
June 13 - 14, 2013
Los Angeles CA US
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FDA Inspections - What Regulators Expect and How to Prepare
June 13 - 14, 2013
Los Angeles CA US
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Medical Devices - Developing Effective Post Market Surveillance and Complaint Handling Systems
June 13 - 14, 2013
Berlin DE
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Analytical Method Validation for Pharmaceutical, Biopharmaceutical, and Biologics Quality Control
June 17 - 18, 2013
Los Angeles CA US
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Process Validation for Drugs and Biologics
June 17 - 18, 2013
Los Angeles CA US
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Pharmaceutical Production Batch Record Review
June 17 - 18, 2013
Los Angeles CA US
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QA/QC Strategy for Biopharmaceuticals and Biologics
June 19 - 21, 2013
Los Angeles CA US
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3rd Next-Generation Sequencing Conference
June 19 - 21, 2013
San Francisco CA US
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4th RNAi Research & Therapeutics Conference
June 20, 2013
San Francisco CA US
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
June 26 - 27, 2013
Los Angeles CA US
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8th Annual Global Pharma Manufacturing Summit 2013
June 27 - 28, 2013
Boston MA US
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July 2013 [+] (13 total)
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Biostatistics for Non-Statisticians
July 8 - 10, 2013
Los Angeles CA US
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Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices
July 8 - 10, 2013
Los Angeles CA US
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8th Protein Kinases in Drug Discovery Conference
July 8 - 9, 2013
Boston MA US
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11th Vaccines Research and Development: All Things Considered
July 8 - 10, 2013
Boston MA US
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2nd Influenza Research and Development
July 8 - 10, 2013
Boston MA US
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 15 - 16, 2013
King of Prussia PA US
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Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
July 15 - 16, 2013
King of Prussia PA US
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Lyophilization Technology – Practical Application of the Scientific Principles
July 15 - 16, 2013
Los Angeles CA US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
July 16 - 17, 2013
Los Angeles CA US
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Medical Devices - Developing Effective Post Market Surveillance and Complaint Handling Systems
July 18 - 19, 2013
King of Prussia PA US
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How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
July 22 - 23, 2013
Los Angeles CA US
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Recent FDA Approval Trends – What You Should Know
July 22 - 23, 2013
Los Angeles CA US
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GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
July 29 - 30, 2013
Los Angeles CA US
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August 2013 [+] (10 total)
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Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
August 1 - 2, 2013
King of Prussia PA US
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Good Laboratory Practices for Pre-Clinical Testing
August 5 - 6, 2013
Los Angeles CA US
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Active Pharmaceutical Ingredient (API) and Drug Product Specifications
August 5 - 7, 2013
Los Angeles CA US
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Stability Programs for Product Shelf Life - From Development to Approval
August 8 - 9, 2013
Los Angeles CA US
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The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
August 12 - 13, 2013
King of Prussia PA US
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
August 12 - 13, 2013
Los Angeles CA US
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Introduction to Effective Medical Writing
August 12 - 13, 2013
Los Angeles CA US
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
August 19 - 21, 2013
Los Angeles CA US
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Introduction to Molecular Biology Techniques
August 19 - 21, 2013
King of Prussia PA US
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Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
August 22 - 23, 2013
Los Angeles CA US
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September 2013 [+] (17 total)
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Validation of Computer Systems
September 9 - 10, 2013
King of Prussia PA US
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How to Implement Risk Management Principles and Activities within a Quality Management System
September 9 - 10, 2013
King of Prussia PA US
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Selecting and Managing CROs
September 9 - 10, 2013
King of Prussia PA US
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6th CNS Partnering and Deal Making Conference
September 9 - 10, 2013
Boston MA US
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7th Neurodegenerative Conditions Research & Development Conference
September 9, 2013
Boston MA US
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Clinical Document Management - A Trial by Trial Approach to Compliance
September 11 - 12, 2013
King of Prussia PA US
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Process Validation for Medical Devices
September 11 - 13, 2013
King of Prussia PA US
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Validation of Computer Systems
September 16 - 17, 2013
Berlin DE
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Preparing the CMC Section for NDAs-CTDs-INDs
September 16 - 17, 2013
Los Angeles CA US
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4th Biobased Chemicals: Commercialization & Partnering Conference
September 16 - 17, 2013
San Francisco CA US
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Introduction to Medical Combination Products
September 17 - 18, 2013
King of Prussia PA US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
September 17 - 18, 2013
Berlin DE
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 18 - 20, 2013
King of Prussia PA US
Read more... -
Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions
September 19 - 20, 2013
King of Prussia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
September 19 - 20, 2013
Berlin DE
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12th Annual Biological Production Forum 2013
September 23 - 25, 2013
Düsseldorf DE
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Pharmaceutical Production Batch Record Review
September 30, 2013 - October 1, 2013
King of Prussia PA US
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October 2013 [+] (29 total)
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Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
October 2 - 4, 2013
King of Prussia PA US
Read more... -
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
October 3 - 4, 2013
King of Prussia PA US
Read more... -
Best Practices for an Effective Cleaning Validation Program
October 7 - 8, 2013
King of Prussia PA US
Read more... -
FDA Inspections: What Regulators Expect and How to Prepare
October 7 - 8, 2013
King of Prussia PA US
Read more... -
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
October 7 - 9, 2013
King of Prussia PA US
Read more... -
Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
October 8 - 9, 2013
King of Prussia PA US
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Good Manufacturing Practices
October 9 - 11, 2013
King of Prussia PA US
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
October 10 - 11, 2013
King of Prussia PA US
Read more... -
Introduction to Statistical Analysis of Laboratory Data
October 14 - 15, 2013
King of Prussia PA US
Read more... -
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
October 14 - 15, 2013
King of Prussia PA US
Read more... -
Process Validation for Drugs and Biologics
October 14 - 15, 2013
King of Prussia PA US
Read more... -
Writing in the Regulated Environment When English Is Your Second Language
October 14 - 15, 2013
King of Prussia PA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
October 16 - 17, 2013
King of Prussia PA US
Read more... -
Effective Risk-Based Applications of Drug cGMPs and Validation Requirements of Cosmetics and OTC Drug Products
October 16 - 17, 2013
King of Prussia PA US
Read more... -
Biostatistics for Non-Statisticians
October 16 - 18, 2013
King of Prussia PA US
Read more... -
Clinical Document Management - A Trial by Trial Approach to Compliance
October 21 - 22, 2013
Berlin DE
Read more... -
How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
October 21 - 22, 2013
King of Prussia PA US
Read more... -
Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
October 21 - 22, 2013
King of Prussia PA US
Read more... -
Lyophilization Technology – Practical Application of the Scientific Principles
October 21 - 22, 2013
Berlin DE
Read more... -
Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices
October 23 - 25, 2013
Berlin DE
Read more... -
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
October 23 - 24, 2013
King of Prussia PA US
Read more... -
QA/QC Strategy for Biopharmaceuticals and Biologics
October 23 - 25, 2013
King of Prussia PA US
Read more... -
Design Control for Medical Device Professionals
October 28 - 29, 2013
King of Prussia PA US
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Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
October 28 - 29, 2013
Berlin DE
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
October 29 - 30, 2013
King of Prussia PA US
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Design Validation, Verification, and Risk Analysis for Medical Device Professionals
October 30 - 31, 2013
King of Prussia PA US
Read more... -
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
October 31, 2013 - November 1, 2013
King of Prussia PA US
Read more... -
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
October 31, 2013 - November 1, 2013
King of Prussia PA US
Read more... -
Auditing and Qualifying Suppliers and Vendors
October 31, 2013 - November 1, 2013
King of Prussia PA US
Read more...
November 2013 [+] (19 total)
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
November 4 - 6, 2013
Berlin DE
Read more... -
Biosimilars – Understanding the Regulatory Challenges
November 4 - 5, 2013
King of Prussia PA US
Read more... -
Clinical Trial Design for Medical Devices
November 4 - 5, 2013
Los Angeles CA US
Read more... -
Introduction to Effective Medical Writing
November 4 - 5, 2013
King of Prussia PA US
Read more... -
Medical Devices: EU Directives, Guidance, CE Marking and
November 4 - 5, 2013
Los Angeles CA US
Read more... -
Recent FDA Approval Trends – What You Should Know
November 4 - 5, 2013
Berlin DE
Read more... -
The EU Clinical Trial Directive
November 4 - 5, 2013
King of Prussia PA US
Read more... -
Pediatric Clinical Trial Design
November 6 - 7, 2013
Los Angeles CA US
Read more... -
Navigating Latin American Regulatory Compliance Requirements for Clinical Trials
November 6 - 7, 2013
Los Angeles CA US
Read more... -
The Drug Development Process - From Discovery to Commercialization
November 6 - 8, 2013
King of Prussia PA US
Read more... -
Understanding GMP Expectations for PET Drug Production
November 6 - 8, 2013
King of Prussia PA US
Read more... -
Medical Devices - Developing Effective Post Market Surveillance and Complaint Handling Systems
November 7 - 8, 2013
Los Angeles CA US
Read more... -
Adverse Drug Events – Understanding and Reporting Requirements
November 11 - 12, 2013
King of Prussia PA US
Read more... -
Cleanroom Microbiology for the Non-Microbiologist
November 11 - 12, 2013
King of Prussia PA US
Read more... -
Process Validation for Medical Devices
November 13 - 15, 2013
Berlin DE
Read more... -
Sterilization Procedures: Introduction to the Science and Methods
November 13 - 14, 2013
King of Prussia PA US
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Comprehensive Overview of European Regulatory Procedures - EU and Member State Submission Requirements
November 14 - 15, 2013
Berlin DE
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Advanced Topics in Biostatistics for Non-Statisticians
November 14 - 15, 2013
King of Prussia PA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
November 18 - 19, 2013
King of Prussia PA US
Read more...
December 2013 [+] (10 total)
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Pharmaceutical Production Batch Record Review
December 2 - 3, 2013
Berlin DE
Read more... -
The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
December 2 - 3, 2013
King of Prussia PA US
Read more... -
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
December 2 - 4, 2013
King of Prussia PA US
Read more... -
Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
December 5 - 6, 2013
Los Angeles CA US
Read more... -
Introduction to Effective Medical Writing
December 5 - 6, 2013
Berlin DE
Read more... -
Good Laboratory Practices for Pre-Clinical Testing
December 9 - 10, 2013
King of Prussia PA US
Read more... -
Preparing the CMC Section for NDAs-CTDs-INDs
December 9 - 10, 2013
King of Prussia PA US
Read more... -
Validation of Computer Systems
December 9 - 10, 2013
Los Angeles CA US
Read more... -
Stability Programs for Product Shelf Life - From Development to Approval
December 9 - 10, 2013
Berlin DE
Read more... -
Active Pharmaceutical Ingredient (API) and Drug Product Specifications
December 11 - 13, 2013
Berlin DE
Read more...
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