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Webinar On Robust Corrective And Preventive Action

 
  May 11, 2015  
     
 


Compliance Trainings, Online
2015-06-03


This 90 minute in-depth webinar will provide valuable assistance to all regulated companies that need to review and modify their company's CAPA system.

 

Its principles apply to personnel / companies in the Medical Devices, Pharmaceutical, Diagnostic, and Biologics fields. 

Areas Covered in the Session :

Regulatory "Hot Buttons"

CAPA Background

Correction, Corrective Action, Preventive Action Defined

Impact Analysis and Response - a Key Component

CAPA System Assessment

"Bullet-Proof"

Data Sources / Metrics

Monitor for Effectiveness

"Closed-Loop" - Lock In the Change

Beyond Regulatory Compliance

 

Who Will Benefit:

The employees who will benefit include:

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 : #416-915-4458 

Email : support@compliancetrainings.com 

 
 
Organized by: Compliance Trainings
Invited Speakers:

John E. Lincoln, is Principal of J. E. Lincoln and Associates LLC, a consulting company with over 33 years experience in U.S. FDA-regulated industries, 19 years as a full-time consultant. John has worked with companies from start-up to Fortune 100, in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan. He specializes in quality assurance, regulatory affairs, QMS problem remediation and FDA responses, new / changed product 510(k)s, process / product / equipment including QMS and software validations, ISO 14971 product risk management files / reports, Design Control / Design History Files, Technical Files.

 
Deadline for Abstracts: 2015-06-03
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1542

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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