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Webinar On CAPA – Corrective Action Preventive Action

 
  May 11, 2015  
     
 


Compliance Trainings, Online
2015-05-19


Description :

How CAPA’s are executed and managed is crucial to maintaining a compliant organization. Inadequate failure investigations continue to be a major GMP deficiency and consistently make the FDA’s top five list for adverse observations. 

This course highlights the various regulations governing CAPAs, how CAPAs are successfully initiated and managed, and how an effective failure investigation and root cause analysis is accomplished.

The primary objective of this webinar is to heighten awareness of the importance of the proper execution of the CAPA process to the organization, to the efficacy of the product and the process, and to the safety of patients and customers.

During this webinar, emphasis is placed on the application and practical aspects of the process to include its critical steps, CAPA timing, participants to the process, roles and functions, and the pitfalls associated with CAPA investigations.

The content of the webinar will focus on the practical and how to best thoroughly accomplish an effective CAPA.

Areas Covered in the Session :

CAPA defined

CAPA relevant regulations

Exception/deviation reporting

CAPA process flow

CAPA process steps explained

Challenges and pitfalls of CAPA’s

CAPA and risk mitigation

 

Who Will Benefit:

A must attend webinar for all personnel / companies in the Pharmaceuticals, Medical Devices, Biotechnology, Cosmetics, Personal Products, Foods & Beverages fields. The professionals who will benefit include all:

Manufacturing Department

Regulatory Affairs

Quality Professionals

Documentation department

Compliance officer

Product Development Professionals

QA/QC analysts

Internal Auditors

Quality Assurance scientists

Production

Operations

Consultants

Quality Unit managers and supervisors

Training Managers and Directors

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:

Speaker Profile

Charles Paul is an instructional designer and management consultant with over 30 years’ experience providing training and consulting services to regulated industries. He has installed quality systems and designed and developed GMP and operational documentation and train, ing programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.

 
Deadline for Abstracts: 2015-05-19
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1463

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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