All device Events (83)

2-day In-person Seminar on Submitting Marketing Applications in Canada at Seattle, Washington

June 18, 2015 at 9am to June 19, 2015 at 6pm – Courtyard Seattle Sea-Tac Area Overview: Topics included will include the filing of New Drug Submissions for various types of pharmaceutical companies, priority submissions, organization of Health Canada, process for approval of a… Organized by GlobalCompliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining

Seminar on How to Conduct Medical Device Risk Analysis Effectively at SFO, CA

July 2, 2015 at 9am to July 3, 2015 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport Overview: Why companies are prone to having past problems in new devices? One of the main reasons seems to be the �weak cognition.� It is usually the result of short term memory, inattention to detai… Organized by GlobalCompliancePanel | Type: food, fda, medical, device, defence, and, navy, aerospace, mining

Applied Statistics for QA, QC, Manufacturing, and Design Control at SFO

July 9, 2015 at 9am to July 10, 2015 at 6pm – DoubleTree by Hilton Hotel San Francisco Airport Course "Applied Statistics for QA, QC, Manufacturing, and Design Control" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completi… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Design of Experiments (DOE) for Process Development and Validation at Singapore

July 9, 2015 at 9am to July 10, 2015 at 6pm – Mandarin Orchard Singapore Overview: Prior to developing a process control plan as part of an overall risk management strategy, process development studies must be completed. The objective of these process development studies… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining

Applied Statistics for Scientists and Engineers at Zurich, Switzerland

July 16, 2015 at 9am to July 17, 2015 at 6pm – Zurich, Switzerland Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteri… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Tougher Import Rules for FDA Imports in 2015 at San Diego, CA

July 16, 2015 at 9am to July 17, 2015 at 6pm – DoubleTree by Hilton Hotel San Diego Downtown Overview: FDA's and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of information and adherence to government procedures. F… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Problem Solving and Root Cause Analysis - the Key to an Effective CAPA System at San Diego, CA

July 16, 2015 from 9am to 6pm – DoubleTree by Hilton Hotel San Diego Downtown Overview: This program is designed to provide participants with: Understanding and developing an effective Corrective and Preventive Action System An understanding of a structured problem solving pr… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining

Seminar on Why You Should be worried about HIPAA at Washington

July 23, 2015 at 9am to July 24, 2015 at 6pm – Courtyard by Marriott Capitol Hill/Navy Yard Overview: We will be discussing the history and evolution of HIPAA Privacy/Security and the major points you need to understand to proactively protect your practice or business. Specific areas covere… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Seminar on Clinical Drug Development and Approval Process at Washington

July 23, 2015 at 9am to July 24, 2015 at 6pm – Washington DC Overview: Drug development is the process of incorporating data from multiple disciplines into a logical and coherent argument for the efficacy and safety of a drug product resulting in regulatory ap… Organized by GlobalCompliancePanel | Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining