Turn a Culture of Quality Into a Competitive Advantage

  • 150.00 Dollar US$
  • Published date: February 22, 2019
    • Fremont, California, United States

Overview:
A culture of quality is a powerful tool for creating an effective and efficient Quality Management System. A culture of quality is not accidental but can be purposefully nurtured and developed.

Why should you Attend:
Every organization has stakeholders. Your customers demand safe and effective medical devices. The regulators expect you to follow the regulations for your markets with resulting product quality and compliance.

Areas Covered in the Session:
Roles and responsibilities
The case for quality
Stages of quality and compliance culture
Tools and techniques for improvement
Best Practices

Who Will Benefit:
Quality Engineers
Compliance Specialists
Compliance Managers and Directors
Quality Managers and Directors
Consultants and Contractors

Speaker Profile:
Susanne Manz ,MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com

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

  • Audit Trail Generation and Review 2019

    Audit Trail Generation and Review 2019

    Other Services Fremont (California) February 22, 2019 150.00 Dollar US$

    Overview: These electronic records must be maintained according to regulatory requirements contained within FDA's 21 CFR Part 11 for US jurisdictions and Eudralex Volume 4 Annex 11 for EU jurisdictions. Why should you Attend: Attendees will learn how...

  • Theory and Practice of Near-Infrared Spectroscopy

    Theory and Practice of Near-Infrared Spectroscopy

    Other Services Fremont (California) January 23, 2019 150.00 Dollar US$

    Overview: NIR is more complex than typical spectroscopic methods. This webinar will compare and contrast NIRS with “commonly used” spectrometers, now in use and more familiar to analysts. Why should you Attend: These can be hand-held, lab-based, or i...

  • Virtual Seminar on Phase I GMPs

    Virtual Seminar on Phase I GMPs

    Other Services Fremont (California) January 21, 2019 545.00 Dollar US$

    Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy subjects and use lower doses of the drug product. Therefore, only small amounts of investigational material are required. I...