dc.rights.license | All rights reserved | en_US |
dc.contributor.advisor | Torres, Edgar | |
dc.contributor.author | Sepúlveda Figueroa, Héctor | |
dc.date.accessioned | 2020-09-17T12:37:47Z | |
dc.date.available | 2020-09-17T12:37:47Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Sepúlveda Figueroa, H. (2014). Quality risk management strategies for computer systems validation [Unpublished manuscript]. Graduate School, Polytechnic University of Puerto Rico. | en_US |
dc.identifier.uri | http://hdl.handle.net/20.500.12475/717 | |
dc.description | Design Project Article for the Graduate Programs at Polytechnic University of Puerto Rico | en_US |
dc.description.abstract | Quality Risk Management is something
that has been gaining attention in the regulated
industry because it is listed as regulation in various
regulatory agencies such as FDA, ICH, ISO, ISPE
and other involved regulatory agencies, but all with
the same goal of improving the and manufacturing
quality of a product manufactured for the patient to
be administered. From this part briefly assess how
QRM strategy works by Good Manufacturing
Practices, and regulatory requirements and
associated guidance documents, making certain
methodology on QRM to CSV is presented. We must
take into account that there is no fixed for all
situations that arise in a given time methodology.
The competent professional is the best person to
select which type of methodology will do the QRM
to be adjusted to the problem presented in the areas
related to computer systems. In this article we
present how we can achieve risk reduction through
QRM in CSV.
Key Terms - Computer Systems Validation,
Quality Risk Management, Risk Reduction,
Strategies. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Polytechnic University of Puerto Rico | en_US |
dc.relation.ispartof | Manufacturing Engineering; | |
dc.relation.ispartofseries | Winter-2014; | |
dc.relation.haspart | San Juan | en_US |
dc.subject.lcsh | Risk management | |
dc.subject.lcsh | Pharmaceutical industry--Quality control | |
dc.subject.lcsh | Pharmaceutical industry--Management | |
dc.subject.lcsh | Health facilities--Risk management | |
dc.subject.lcsh | Pharmaceutical industry--Data processing | |
dc.subject.lcsh | Polytechnic University of Puerto Rico--Graduate students--Research | |
dc.title | Quality Risk Management Strategies for Computer Systems Validation | en_US |
dc.type | Article | en_US |
dc.rights.holder | Polytechnic University of Puerto Rico, Graduate School | en_US |