Overview of Device Regulation – FDA 2017

  • 1295.00 Dollar US$
  • Published date: April 24, 2017
    • Boston, MA, Boston, MA, United States

Course "Overview of Device Regulation - FDA" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways.

Why should you attend:
This course provides a basic description of an FDA regulatory strategy for medical devices and explains the relationships between regulatory strategy and product development. It offers guidelines for developing successful strategies for medical devices, including definitions and classifications, elements of regulatory strategy, sources of regulatory intelligence, selection of development and product clearance/approval pathways.

Location: Boston, MA Date: June 22nd & 23rd, 2017 and Time: 8:30 AM to 5:30 PM

Venue: Embassy Suites Boston Logan Airport
Address: Embassy Suites Boston Logan Airport 207 Porter Street Boston, MA 02128

Price:

Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until May 10, Early Bird Price: $1,295.00 From May 11 to June 20, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*


Quick Contact:
NetZealous DBA as GlobalCompliancePanel
Phone: 1-800-447-9407
Fax: 302-288-6884
Email: john.robinson@globalcompliancepanel.com
Website: http://www.globalcompliancepanel.com

Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900902SEMINAR?science-marketplace_SEO
Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel
Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/
Follow us on Twitter: https://twitter.com/GCPanel

Result 0 votes
John Robinson
0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • Medical Devices Industry and Risk Management 2017

    Medical Devices Industry and Risk Management 2017

    Training and Teaching Boston, MA (Boston, MA) April 24, 2017 1295.00 Dollar US$

    Overview: Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifec...

  • Medical Device Single Audit Program for Compliance Success (MDSAP) 2017 before 30 April 50% Discount

    Medical Device Single Audit Program for Compliance Success (MDSAP) 2017 before 30 April 50% Discount

    Training and Teaching Boston, MA (Boston, MA) March 24, 2017 1295.00 Dollar US$

    Reviewing the most significant changes affecting medical device standards and guidance documents Understanding the MDSAP (goals and strategy) Analyzing the MDSAP main differences with standard auditing Understanding grading of MDSAP non-conformances ...

  • Laboratory, Medical and Device Performance and Validation following Regulatory 2017-50% Discount

    Laboratory, Medical and Device Performance and Validation following Regulatory 2017-50% Discount

    Training and Teaching Boston, MA (Boston, MA) March 24, 2017 1295.00 Dollar US$

    This course is designed to introduce to individuals the understanding and interpretation of the statistical concepts one uses when investigating quantitative ICH Guidelines such as analytical methods validation, procedures and acceptance criteria in ...