MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Webinar On Robust Verification and Validation

Event Details

Webinar On Robust Verification and Validation

Time: February 10, 2015 from 1pm to 2:30pm
Location: Online
Street: 5939 Candlebrook Ct
City/Town: Mississauga
Website or Map: https://compliancetrainings.c…
Phone: 4169154458
Event Type: webinar
Organized By: Compliance Trainings
Latest Activity: Jan 16, 2015

Export to Outlook or iCal (.ics)

Event Description

Description :

This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies, many going back to insufficient, poor or non-existent V&V planning.

And now the FDA is taking an even tougher stance.

Why do companies need robust V&V?

What are the "must have" elements from  the cGMPs?

How do ISO 14971 and ICH Q9 for hazard analysis and product risk management factor in and assist to allocating limited company resources?

How can these be integrated into the company's quality management system?

Areas Covered in the Session :

Robust Verification and Validation -- Recent Regulatory requirements.

The Master Validation Plan(s).

Individual Verification and Validation Plans and their execution.

Product Verfication & Validation.

Process and Equipment Verfication & Validation, including Software.

QMS V&V and 21 CFR Part 11.

When and How to Use DQ, IQ, OQ, PQ, or ASTM E2500 Equivalents.

The 11 Elements of the FDA's Software V&V "Model".

Incorporate the Hazard Analysis / Risk Management tools of ISO 14971 and ICH Q9.

Avoid recent compliance problems.

Who Will Benefit:

This webinar will provide valuable assistance to all regulated companies that need to review and modify their company's planning and execution of verification and validation. Its principles apply to personnel / companies in the Medical Devices, Pharmaceutical, Diagnostic, and Biologics fields. The professionals who will benefit include all:

Senior management

Middle management

R&D

Engineering

Software

QA / RA

Manufacturing

Operators

Consultants

cGMP instructors

And all personnel involved in verification and/or validation planning, execution and documentation.

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : 4169154458 
Email : support@compliancetrainings.com

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1268

Like Us On facebook:

https://www.facebook.com/events/1520183291579565/?source=1&sid_create=80105171

Comment Wall

Comment

RSVP for Webinar On Robust Verification and Validation to add comments!

Join MedTech I.Q.

Attending (1)

© 2024   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service