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Global Medical Device Regulation: US, EU and Canada Sep 2014

Events & Concerts

(Free Press Release) GlobalCompliancePanel proudly presents its upcoming In-Person seminar on “Global Medical Device Regulation: US, EU and Canada” by Dr. Thomas E. Colonna, Founder, Biotech Consultant LLC in Chicago, IL on September 4th & 5th, 2014 .

Global Medical Device Regulation: US, EU and Canada Sep 2014


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Chicago, IL, USA., July 29, 2014 - (PressReleasePoint) -

Overview of the Course:
This course provides an overview of international medical device regulations. Beginning with a discussion of the similarity of global requirements, including both voluntary and mandatory standards and directives, and progressing to in-depth analyses of market specific requirements, the course provides the student with resources to meet the regulatory requirements for the largest world markets. Country-specific regulatory requirements for Canada, EU, and US are included.

Reasons to Attend this Valuable Session:
This course provides a basic description of global regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful global strategies for medical devices, including definitions and classifications worldwide, elements of regulatory strategy, sources of regulatory intelligence, and selection of development and product approval pathways.

Areas Covered in the Session:

·         Describe the elements impacting the definition and classification of medical devices globally
·         Determine the points to consider in the development of a global regulatory strategy
·         Define the tools for global regulatory strategy development
·         Recognize sources of regulatory and competitive intelligence
·         Identify the elements of a regulatory plan
·         Apply global regulatory principles to develop a regulatory plan

The List of Individuals for whom this Course will be benefited:
Regulatory professionals working in the medical device field.

Meet your Expert:
Dr. Thomas E. Colonna earned a bachelor of science in microbiology from the University of Sciences in Philadelphia (formerly the Philadelphia College of Pharmacy and Science), a Ph.D. in molecular biology from the Johns Hopkins University, and a law degree from the Georgetown University Law Center. In addition, Dr. Colonna holds academic appointments at Johns Hopkins University and the University of Sciences in Philadelphia.
Dr. Colonna provides consulting services in the scientific and regulatory aspects of a wide range of medical devices and biologics with particular expertise in the areas of in vitro diagnostics (ELISA-based, PCR-based, SNPs, microarrays, and pharmacogenomics), medical device software (including bioinformatics), and biotechnology-based products. Dr. Colonna's consulting clients range from Fortune 500 companies to small start-up companies located throughout the US, as well as, Canada, India, and Russia. Widely published in numerous fields, Dr. Colonna brings a unique multidisciplinary approach to problem solving.
Date: September 4th & 5th, 2014, 9 AM to 5 PM
Location & Venue: Courtyard Chicago O'Hare   2950 S. River Road Des Plaines Illinois 60018 USA

For Registration, Click on the link below: https://www.globalcompliancepanel.com/control/~product_id=900090SEMINAR

GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management.

Our Achievements:

  • Over 300 Experts that are Renowned in their Respective Areas
  • Successfully Trained more than 20,000 Compliance Professionals
  • A Most Comprehensive Portal for Trainings, Industry Updates and Professional Growth
  • Having more than 2000 Online Courses
  • Successfully Completed more than 170 Seminars in US and Globally

Global Medical Device Regulation: US, EU and Canada Sep 2014

Source: Press Release



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