FDAnews Announces — Internal Auditing Using the MDSAP Model Webinar, July 27, 2016

Share Article

Don’t be one of the 75% of device manufacturers who conduct internal audits solely “because manufacturers have to — because the FDA and ISO regs say so?” Instead of cringing at the idea of conducting an internal audit, consider implementing the Medical Device Single Audit Program (MDSAP) model.

Internal Auditing Using the MDSAP Model
**An FDAnews Webinar**
July 27, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://www.fdanews.com/internalauditingmdsapmodel

Don’t be one of the 75% of device manufacturers who conduct internal audits solely “because manufacturers have to — because the FDA and ISO regs say so?”

Instead of cringing at the idea of conducting an internal audit, consider implementing the Medical Device Single Audit Program (MDSAP) model. It’s a single audit of the quality management system and satisfies medical device regulatory authorities.

Join Susan Reilly on July 27 for a 90-minute webinar where she’ll teach attendees how to build and implement a highly effective, independent internal audit program including:

  •     How to conduct an audit covering the standards and regulations addressed under the MDSAP model
  •     How to identify and understand the requirements as interpreted by the various regulatory authorities
  •     How to determine gaps in the current documentation
  •     How to “score" the current quality system
  •     How to improve the predictability of an audit outcome
  •     How to report the audit findings using a standard report template
  •     The benefits of enrolling in the MDSAP

Register today and get MDSAP up and running.

Meet the Presenter:
Susan Reilly, Reilly Associates LLC

Susan Reilly has more than 25 years of quality system, quality engineering, and regulatory compliance experience in the medical device area. Her company provides practical and cost-effective quality and regulatory consulting services to ensure conformance with FDA regulations, EU requirements, Canadian requirements, and ISO Standards.

Who Will Benefit:

  •     Medical device manufacturing and executives
  •     Auditing and compliance officers
  •     QA/QC managers and directors
  •     Production managers
  •     Production supervisors
  •     Process development staff
  •     Auditing and compliance officers
  •     Training managers
  •     Regulatory affairs professionals
  •     Executive management
  •     General/corporate counsel
  •     Personnel new to the industry

Webinar Details:
Internal Auditing Using the MDSAP Model
**An FDAnews Webinar**
July 27, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://www.fdanews.com/internalauditingmdsapmodel

Tuition:
$287 per site

Easy Ways to Register:
Online:     http://www.fdanews.com/internalauditingmdsapmodel        
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

Share article on social media or email:

View article via:

Pdf Print

Contact Author

Michelle Butler
FDANEWS
+1 (703) 538-7665
Email >
FDAnews
Like >
Visit website