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Webinar On Effective Purchasing & Supplier Controls in Accordance with 21 CFR, Part 820.50

 
  May 22, 2015  
     
 


Compliance Trainings, Online
2015-06-09


Description :

Lack of an effective approach to purchasing controls and supplier management is one of the more frequent Form 483 observations cited during FDA device establishment inspections. Additionally, problems with purchasing controls are typically rooted in a lack of effective supplier controls, which also falls under the realm of §820.50. In fact, the lack of effective purchasing and supplier controls often result in product recalls due to nonconforming product finding its way into the supply chain.

If your organization is struggling with understanding the salient requirements associated with purchasing and supplier controls, this webinar is for you. This webinar will help your organizations better understand the FDA’s expectations for purchasing and supplier controls, while providing insight into tools needed for establishing an effective approach for purchasing and supplier management. For establishments already having a compliant purchasing controls system, this webinar will help your organization streamline their approach to purchasing and supplier management.

Areas Covered in the Session :

Reviewing and understanding the requirements associated with 21 CFR, Part 820.50 compliance.

Similarities with ISO 13485, Clause 7.4.

Understanding current industry practices.

Purchase orders, contracts, & supplier agreements.

Establishing a proactive approach to supplier evaluations.

Understanding the components of supplier risk.

Managing suppliers.

The supplier selection process.

Employing categories for supplier management.

Supplier quality agreements.

No-change agreements.

Establishing supplier metrics and report cards.

Supplier Corrective Action Requests (SCARs).

Supplier Removal process from the Approved Supplier’s List (ASL)

Assessing tier 2 suppliers.

Acceptance activities (receiving inspection).

Recent FDA enforcement activities.

Who Will Benefit:

A must attend webinar for all industry professionals, regardless of functional roles, will benefit from this training, especially if you are involved in the day-to-day activities associated with your organization’s purchasing and supplier management process. The staff who will benefit include:

Quality Professionals

Regulatory Professionals

Test Technicians

R & D Engineers

Manufacturing Engineers

Quality Engineers

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: Dr. Christopher Joseph Devine is the president and founder of Devine Guidance International, Inc., (DGII) a consulting firm providing regulatory and quality compliance support for the medical device industry. Prior to launching DGII, Dr. D spent 14-years with Boston Scientific Corporation working in a variety of quality and regulatory management roles. Additionally, Dr. Devine is the author of Devine Guidance, a weekly blog focusing on quality and regulatory compliance issues facing the medical device industry; and published by the Medical Device Summit, an e-magazine.


 
Deadline for Abstracts: 2015-06-09
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1445

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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