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Webinar On Line Clearance – Compliance Implications, Enforcement, and Best Practices

 
  June 22, 2015  
     
 


Compliance Trainings, Online
2015-07-09


Description :

Within the Pharmaceutical Industry, the changeover from one product to another on a filling/packaging line, although relatively a simple concept, has significant implications from a regulatory standpoint if cross-contamination is permitted to occur. Preventing cross-contamination requires a precise accountable process to be properly executed.

Within the industry, there is significant confusion concerning line clearance, cleaning and reconciliation. Often, these three distinctly different processes are intermingled diminishing the effectiveness of each. This webinar will present industry best practices for the documentation, execution, and accountability of line clearance. Line clearance documentation requirements are particularly important to effective line clearance performance and the FDA has specific expectations when it comes to that documentation.

Areas Covered in the Session :

Line clearance defined

Relationship between line clearance, cleaning, and reconciliation

Line clearance case studies

Line clearance documentation – preparation and utilization

Line clearance responsibilities and accountabilities

Line clearance execution

Who Will Benefit:

A must attend webinar for Anyone involved in the manufacturer of pharmaceutical products and that has had some exposure to the subject area. A recommended webinar for Professionals in the departments of:

Quality

Production

Compliance

Supervisory personnel

Everyone with packaging line responsibilities

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:

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 training programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.

 
Deadline for Abstracts: 2015-07-09
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1465

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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