On-demandOn-demand

Audits and Inspections: How to Drive a Standardization Strategy that Sticks (On-Demand)

1.0 RAC Credits Member: $0 NonMember: $25
Audits and Inspections: How to Drive a Standardization Strategy that Sticks (On-Demand)

This is an on-demand recording from June 22, 2022


Quality, compliance and regulatory professionals love standardization - and your auditors will look for it too. Doing the same things the same way across your business slices risk, strengthens your processes and embeds robust, repeatable quality.

Targeted audits and inspections are your secret weapon for driving a standardization program that actually works. Join our webinar to hear top tips and tactics, mistakes to avoid and detailed guidance to start working to a stronger, more standardized business operation.

Learning Objectives

After this program, participants will:

  • Why standardization is the key to world class regulatory and quality management
  • How audits and inspections are your secret standardization weapon
  • Top tips and operational tactics for a targeted standardization strategy
  • Expert guidance and experience from our speakers at Qualio and Rimsys

Who Should Attend?

  • Quality Assurance
  • Regulatory Affairs
  • R&D
  • Clinical Operations
  • Manufacturing
  • Executives/Directors
  • Product Managers
  • Senior Managers
  • Clinical Research Staff

Pricing Amounts & Deadlines

Free

Instructors:

Kelly Stanton

Kelly Stanton
Director Of Quality, Qualio

Kelly leads Qualio’s in-house quality team and spearheads the company's Qualio+ QA support service. Kelly has built over 20 years of experience working with quality teams at Abbott, Sandoz, Cochlear and more, before becoming Qualio's Director of Quality.

Bruce McKean

Bruce McKean
Regulatory Director, Rimsys

Bruce is Regulatory Director of Rimsys and has amassed over 25 years of quality and regulatory experience. With a focus on quality management and international regulatory compliance, Bruce has worked with electromechanical, implantable and SaMD organizations.


Cancellation Policy

RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. To transfer a registration, email support@raps.org with the event title, name of the original registrant and the contact information for the new attendee.

Contact Us

For additional hands-on support, you can also connect with RAPS support 30 min prior to the workshop: https://www.raps.org/website/virtual-event-help

For account support, contact the RAPS Support Center: +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email support@raps.org.

Add to Cart
 

Discover more of what matters to you

Biologics Combination Products Medical Devices Pharmaceuticals

News »

  5;9;18;25;