Quality Control, Safety & Security

Listings
  • 2-day In-person Seminar FDA and U.S. Customs Import Rules and Export Traps in 2020

    2-day In-person Seminar FDA and U.S. Customs Import Rules and Export Traps in 2020

    Quality Control, Safety & Security Washington (Washington, DC) August 8, 2019 2000.00 Dollar US$

    FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an imp...

  • Introduction to Adaptive Design for Clinical Trials

    Introduction to Adaptive Design for Clinical Trials

    Quality Control, Safety & Security Philadelphia (Pennsylvania) October 25, 2018 1495.00 Dollar US$

    Description: This 2-day seminar includes an overview of Adaptive Design, and an emphasis in group sequential design, sample size re-estimation, and Phase II/III Adaptive Seamless Designs. The role of statistics in clinical trials incorporates the too...

  • Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Quality Control, Safety & Security Boston (Massachusetts) July 5, 2018 1295.00 Dollar US$

    This two-day seminar will cover the essentials of an effective yet efficient Quality management system for medical device companies. An efficient and effective Quality System can be a competitive advantage for companies by leading to improved Quality...

  • Course on GxP/GMP Regulations: Requirements Compliance 2018

    Course on GxP/GMP Regulations: Requirements Compliance 2018

    Quality Control, Safety & Security San Diego (California) March 6, 2018 1295.00 Dollar US$

    Overview: GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. GMP regulations describe required quality management system for production and testing of produc...

  • Validation and 21 CFR Part 11 Compliance of Computer Systems

    Validation and 21 CFR Part 11 Compliance of Computer Systems

    Quality Control, Safety & Security Fremont (California) January 21, 2019 545.00 Dollar US$

    This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity....

  • The EU Clinical Trial Regulation - EU Filings & Registrations

    The EU Clinical Trial Regulation - EU Filings & Registrations

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics). The course also covers recent updates on EU-GCP associated with the new regulatory...

  • 6-Hour Virtual Seminar on Clinical Data Management - Part II

    6-Hour Virtual Seminar on Clinical Data Management - Part II

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is...

  • Take Advantage Of 21 Cfr Part 11 - Read [Immediately] These Tips

    Take Advantage Of 21 Cfr Part 11 - Read [Immediately] These Tips

    Quality Control, Safety & Security Fremont (California) November 13, 2018 290.00 Dollar US$

    Overview: These may be used for GxP regulated activities, and they present particular compliance challenges, as Excel and other spreadsheets are not originally designed for the regulated environment. Why should you Attend: CSV enables the level and r...

  • Things To Do Immediately About Master Validation Plan 2019

    Things To Do Immediately About Master Validation Plan 2019

    Quality Control, Safety & Security Fremont (California) November 13, 2018 290.00 Dollar US$

    Overview: How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements. Why should you Attend: The billions of dollars spent by industry annual...

  • Risk Based Incident Management and [CAPA for GxP] Operations

    Risk Based Incident Management and [CAPA for GxP] Operations

    Quality Control, Safety & Security Fremont (California) November 13, 2018 290.00 Dollar US$

    Overview: This Webinar specifically addresses the Incident Management and CAPA processes of the Operations phase of GxP Computerized Systems and describes the development, implementation, and maintenance of efficient, cost-effective, and compliant pr...

  • 3-Hour Virtual Seminar on FDA Imports Require Precision in 2019

    3-Hour Virtual Seminar on FDA Imports Require Precision in 2019

    Quality Control, Safety & Security Fremont (California) May 23, 2019 290.00 Dollar US$

    Overview: After attending this 3-Hour Virtual Seminar, you will have great understanding of how FDA and Customs and Border Protection (CBP) operate a joint program. Why should you Attend: If you understand FDA's and CBP's import program, your busines...

  • Best Mastering Excel Formulas and Functions 2019

    Best Mastering Excel Formulas and Functions 2019

    Quality Control, Safety & Security Fremont (California) February 22, 2019 290.00 Dollar US$

    Overview: Functions are built-in formulas that have been programmed to perform a specific calculation. They range from the simple such as SUM and AVERAGE (used to calculate the total and average of numbers in a range of cells) to the powerful IF and ...