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Course Title Course Date Location
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 Non-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
Validation of Computer Systems Aug 14, 2017 - Aug 15, 2017 Malvern, PA 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
FDA Inspections: What Regulators Expect and How to Prepare Sep 18, 2017 - Sep 19, 2017 Malvern, PA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 20, 2017 - Sep 22, 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
Validation of Computer Systems Oct 16, 2017 - Oct 17, 2017 Boston, MA United States
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ Oct 17, 2017 - Oct 18, 2017 Malvern, PA United States
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
Writing Effective SOP and Other Process Documents Oct 23, 2017 - Oct 24, 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 (HVAC) 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
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices™ 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
Introduction to Effective Medical Writing Nov 06, 2017 - Nov 07, 2017 Malvern, PA 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
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Nov 08, 2017 - Nov 10, 2017 Malvern, PA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Nov 13, 2017 - Nov 14, 2017 Malvern, PA United States
Good Laboratory Practices (GLP) for Non-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
Understanding Sterilization Methods for Products and Devices Nov 15, 2017 - Nov 16, 2017 Malvern, PA 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
Good Laboratory Practices (GLP) for Non-Clinical Testing Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Heating, Ventilation, & Air Conditioning (HVAC) in a Regulated Environment Dec 06, 2017 - Dec 08, 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