Effective FDA and ISO Management Reviews

  • Check with publisher
  • Published date: February 21, 2017
    • Fremont, California, United States

Overview:
In this presentation will cover the requirement for management review from FDA cGMP and ISO 13485 and approaches that can make these effective. Management review should be a key part of keeping your quality management system efficient and effective.

Why should you Attend:
Are your management reviews effective or do you have trouble getting senior management engaged? Perhaps you are not using an effective approach that fits your company or your management.

Areas Covered in the Session:
Understand the requirements of Management Review
How to get Senior Management Buy-In
Making Management Reviews effective

Who Will Benefit:
Quality Systems Management Representatives
Quality Managers
QA Specialists
Quality Engineers

Speaker Profile:
Betty Lane has over 30 years' experience in Medical Device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems. Her work enables companies to manage their business in compliance with FDA and ISO 13485 requirements, as well for quality system requirements for other geographic area such as Europe and Canada.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501222LIVE?channel=mailer&camp=Webinar&AdGroup=marketplace_Apr_2017_SEO

Result 0 votes
Compliance4All
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

  • FDA and ISO Compliance Personnel Training - 2017

    FDA and ISO Compliance Personnel Training - 2017

    Pharmacology - Drug Development Fremont (California) May 15, 2017 Check with publisher

    Overview: To satisfy QSR and ISO 13485 requirements as well as produce quality products, companies must assure personnel are trained on their routine job practices as well as familiar with requirements that impact them. Areas Covered in the Session: ...

  • The Complete Payroll Law and Best Payroll Service 2017

    The Complete Payroll Law and Best Payroll Service 2017

    Pharmacology - Drug Development Baltimore, MD ( Baltimore, MD) February 24, 2017 Check with publisher

    Overview: This course covers a very broad range of topics from worker classification, to employee classification, to establishing methods and rates of pay, what must be included in the rate of pay, hours that must be compensated as worked time, requi...

  • How to Conduct a Human Factors - Test following ISO 62366

    How to Conduct a Human Factors - Test following ISO 62366

    Pharmacology - Drug Development Fremont (California) February 21, 2017 Check with publisher

    Overview: This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation. HF/U validation is very different from device validation. For example, success criteria is qualitat...