Available Courses

Results (75)




Course Title Course Date Location
Biostatistics for Non-Statisticians Mar 01, 2017 - Mar 03, 2017 Berlin, Germany
FDA Inspections: What Regulators Expect and How to Prepare Mar 06, 2017 - Mar 07, 2017 Malvern, PA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Mar 08, 2017 - Mar 10, 2017 Malvern, PA United States
Project Management for Medical Device Product Development Mar 09, 2017 - Mar 10, 2017 Los Angeles, CA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Mar 13, 2017 - Mar 14, 2017 Malvern, PA United States
Writing in the Regulated Environment When English Is Your Second Language Mar 13, 2017 - Mar 14, 2017 Berlin, Germany
Validation of Computer Systems Mar 20, 2017 - Mar 21, 2017 Malvern, PA United States
Understanding Sterilization Methods for Products and Devices Mar 22, 2017 - Mar 23, 2017 Malvern, PA United States
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices™ Apr 03, 2017 - Apr 04, 2017 Malvern, PA United States
Design Control for Medical Device Professionals™ Apr 03, 2017 - Apr 04, 2017 Los Angeles, CA United States
Introduction to Effective Medical Writing Apr 03, 2017 - Apr 04, 2017 Malvern, PA United States
Introduction to Medical Device Submissions – 510(k)s, PMAs, and Exemptions Apr 03, 2017 - Apr 04, 2017 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Apr 05, 2017 - Apr 06, 2017 Los Angeles, CA United States
Introduction to Medical Combination Products Apr 05, 2017 - Apr 07, 2017 Berlin, Germany
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Apr 05, 2017 - Apr 07, 2017 Malvern, PA United States
Validation of Computer Systems Apr 20, 2017 - Apr 21, 2017 Berlin, Germany
Auditing for Medical Devices: ISO 19011:2011 Framework Apr 24, 2017 - Apr 26, 2017 Los Angeles, CA United States
Good Laboratory Practices (GLP) for Pre-Clinical Testing Apr 24, 2017 - Apr 26, 2017 Malvern, PA United States
Introduction to Medical Device Submissions – 510(k)s, PMAs, and Exemptions Apr 24, 2017 - Apr 25, 2017 Los Angeles, CA United States
Auditing for Medical Devices: EN ISO 13485:2016 Changes Apr 26, 2017 - Apr 28, 2017 Los Angeles, CA United States
Introduction to Medical Combination Products Apr 26, 2017 - Apr 28, 2017 Los Angeles, CA United States
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ May 08, 2017 - May 09, 2017 Malvern, PA United States
Writing Effective SOP and Other Process Documents May 10, 2017 - May 11, 2017 Malvern, PA United States
Integration of Risk Management Principles and Activities into the Quality System May 15, 2017 - May 16, 2017 Malvern, PA United States
Process Validation for Medical Devices May 17, 2017 - May 19, 2017 Malvern, PA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems May 22, 2017 - May 23, 2017 Malvern, PA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications May 24, 2017 - May 25, 2017 Malvern, PA United States
Design Control for Medical Device Professionals™ May 30, 2017 - May 31, 2017 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Jun 01, 2017 - Jun 02, 2017 Berlin, Germany
Auditing and Qualifying Suppliers and Vendors™ Jun 05, 2017 - Jun 06, 2017 Los Angeles, CA United States
Auditing for Medical Devices: ISO 19011:2011 Framework Jun 05, 2017 - Jun 07, 2017 Berlin, Germany
Heating, Ventilation, & Air Conditioning in a Regulated Environment Jun 07, 2017 - Jun 09, 2017 Malvern, PA United States
Auditing for Medical Devices: EN ISO 13485:2016 Changes Jun 07, 2017 - Jun 09, 2017 Berlin, Germany
FDA Inspections: What Regulators Expect and How to Prepare Jun 12, 2017 - Jun 13, 2017 Los Angeles, CA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jun 14, 2017 - Jun 16, 2017 Los Angeles, CA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Jul 17, 2017 - Jul 18, 2017 Los Angeles, CA United States
Biostatistics for Non-Statisticians Jul 19, 2017 - Jul 21, 2017 Los Angeles, CA United States
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ Jul 24, 2017 - Jul 25, 2017 Los Angeles, CA United States
Good Laboratory Practices (GLP) for Pre-Clinical Testing Aug 07, 2017 - Aug 09, 2017 Los Angeles, CA United States
Introduction to Effective Medical Writing Aug 07, 2017 - Aug 08, 2017 Los Angeles, CA United States
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Aug 09, 2017 - Aug 11, 2017 Los Angeles, CA United States
Introduction to Medical Device Submissions – 510(k)s, PMAs, and Exemptions Sep 11, 2017 - Sep 12, 2017 Malvern, PA United States
Project Management for Medical Device Product Development Sep 11, 2017 - Sep 12, 2017 Malvern, PA United States
Introduction to Medical Combination Products Sep 13, 2017 - Sep 15, 2017 Malvern, PA United States
Introduction to Effective Medical Writing Sep 25, 2017 - Sep 26, 2017 Berlin, Germany
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Sep 27, 2017 - Sep 29, 2017 Berlin, Germany
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries™ Oct 12, 2017 - Oct 13, 2017 Malvern, PA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 12, 2017 - Oct 13, 2017 Berlin, Germany
Advanced Topics in Biostatistics for Non-Statisticians™ Oct 16, 2017 - Oct 17, 2017 Malvern, PA United States
Integration of Risk Management Principles and Activities into the Quality System Oct 16, 2017 - Oct 17, 2017 Berlin, Germany
Biostatistics for Non-Statisticians Oct 18, 2017 - Oct 20, 2017 Malvern, PA United States
Process Validation for Medical Devices Oct 18, 2017 - Oct 20, 2017 Berlin, Germany
Selecting and Managing CROs Oct 19, 2017 - Oct 20, 2017 Malvern, PA United States
Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices Oct 24, 2017 - Oct 25, 2017 Malvern, PA United States
Heating, Ventilation, & Air Conditioning in a Regulated Environment Oct 25, 2017 - Oct 27, 2017 Berlin, Germany
Writing in the Regulated Environment When English Is Your Second Language Oct 25, 2017 - Oct 26, 2017 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors™ Oct 30, 2017 - Oct 31, 2017 Berlin, Germany
Auditing for Medical Devices: ISO 19011:2011 Framework Oct 30, 2017 - Nov 01, 2017 Malvern, PA United States
Auditing for Medical Devices: EN ISO 13485:2016 Changes Nov 01, 2017 - Nov 03, 2017 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors™ Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
FDA Inspections: What Regulators Expect and How to Prepare Nov 06, 2017 - Nov 07, 2017 Berlin, Germany
Integration of Risk Management Principles and Activities into the Quality System Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Clinical Trial Design For Medical Devices™ Nov 08, 2017 - Nov 09, 2017 Malvern, PA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Nov 08, 2017 - Nov 10, 2017 Berlin, Germany
Process Validation for Medical Devices Nov 08, 2017 - Nov 10, 2017 Los Angeles, CA United States
Good Laboratory Practices (GLP) for Pre-Clinical Testing Nov 13, 2017 - Nov 15, 2017 Berlin, Germany
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Nov 13, 2017 - Nov 14, 2017 Los Angeles, CA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Nov 15, 2017 - Nov 16, 2017 Los Angeles, CA United States
QbD: Product and Process Optimization using Design of Experiments (DoE) Nov 22, 2017 - Nov 24, 2017 Berlin, Germany
Design Control for Medical Device Professionals™ Nov 28, 2017 - Nov 29, 2017 Malvern, PA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
Validation of Computer Systems Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ Dec 11, 2017 - Dec 12, 2017 Berlin, Germany
Understanding & Implementing the New EU Clinical Trial Regulation Dec 11, 2017 - Dec 12, 2017 Malvern, PA United States
Writing Effective SOP and Other Process Documents Dec 13, 2017 - Dec 14, 2017 Berlin, Germany