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Scott
@savery115
Trusted Member
Joined: Dec 28, 2016
Topics: 11 / Replies: 71
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RE: Product Failure

Like many have said I have also been involved in root cause analysis to examine the reasoning behind something failing. In many cases, most of the ro...

7 years ago
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RE: Product Obsolescence

I have experience with evaluating legacy products and obsoleting products. It is usually a bigger undertaking then one would think. To your point, i...

7 years ago
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RE: Technical Writing Skills

I agree with this that the thought process in technical writing in industry is always "if a random person picked up this document, could they understa...

7 years ago
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RE: CAPAs: Proactive vs Reactive

From a business standpoint, you would want to open less CAPAs. In manufacturing of medical devices most CAPAs tend to be reactive since they are usua...

7 years ago
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RE: Maintenance & validation

Ideally in manufacturing it is best practice to have spare equipment in the instance that a machine fails. Therefore, it is a simple task to bring it...

7 years ago
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RE: Discussion Topic: Post-market surveillance

I would like to point out that post market surveillance can also be conducted on clinical studies. The importance of Post Market Clinical Follow Up (P...

7 years ago
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RE: Standard Operating Procedures (SOP's)

Yes, SOPs should be used in research phase. If you are looking to produce a new product to market or making changes to current products in your produ...

7 years ago
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RE: Does your company use ECOs?

The company I currently work for generates ECOs to make specific changes to products or manufacturing processes. Our ECOs are generated in a Product ...

7 years ago
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RE: Regression Verification and Validation

In agreement that acceptance criteria needs to be re-evaluated. Before that, a deviation should be opened to address the failure of a validation and ...

7 years ago
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RE: DHF vs. Tech File/Design Dossier

It depends what you are looking for. The DHF would be more useful all around for people in Quality, Regulatory, Supply Chain, and even Product Develop...

7 years ago
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RE: Discussion Topic: Is the DHF a living document?

The DHF is a living document. Logically to me it doesn't even make sense why it wouldn't be. What is the point of documenting just the original proce...

7 years ago
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RE: Classification in FDA Vs EU

In the US, nonabsorbable sutures can be classified as Class II with moderate risk of injury. In addition, absorbable sutures can be classified as Clas...

7 years ago
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RE: Combination Products in EU

Absolutely. The revisions that have taken place under the Medical Device Directives are meant to be on par or if not more stringent then the US FDA. ...

7 years ago
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RE: Multi-Center Clinical Studies

I don’t believe there should be a defined limit of center or subjects because that should depend fully on what the study is. However, when choosing mu...

7 years ago
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