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GxP Professionals - Welcome

Welcome to GXP Professionals. GxP Professionals specializes in full life cycle development of computer systems for the pharmaceutical industry. We can perform audits on your computer system validation and documentation to prepare for FDA audits. We can assess your product line and determine your process reliability. We can assist in managing your pharmaceutical IT projects from end-to-end. Contact us today for more information.

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Welcome to GXP Professionals. GxP Professionals specializes in full life cycle development of computer systems for the pharmaceutical industry. We can perform audits on your computer system validation and documentation to prepare for FDA audits. We can assess your product line and determine your process reliability. We can assist in managing your pharmaceutical IT projects from end-to-end. Contact us today for more information.
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GxP Professionals - Welcome | gxppro.com Reviews

https://gxppro.com

Welcome to GXP Professionals. GxP Professionals specializes in full life cycle development of computer systems for the pharmaceutical industry. We can perform audits on your computer system validation and documentation to prepare for FDA audits. We can assess your product line and determine your process reliability. We can assist in managing your pharmaceutical IT projects from end-to-end. Contact us today for more information.

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GxP Professionals - Product Assessments

http://www.gxppro.com/pa.html

We can perform a product assessment on your products as well as your Quality Systems. Our product assessment will review your Key Performance Indicators and provide you an analysis of how well your products are performing. Our assessment can include:. Production Data (batch size). Process Data (pH, hardness, speed).

2

GxP Professionals - About Us

http://www.gxppro.com/about.html

GxP Professionals have over 25 years of experience in pharmaceutical IT. Our core competencies include:. 21 CFR Part 11 Assessments. Full life cycle software development.

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GxP Professionals - Project Management

http://www.gxppro.com/pm.html

Our project management skills include:. Identify project bottlenecks and develop workarounds to improve project schedule. Facilitate communication between team members and key departments to allow faster and complete decisions. Lead effective project meetings with agenda, meeting minutes, and decisions thoroughly documented. Microsoft Project - organize tasks to obtain high and low level views of project completion; allocate individuals and reduce over allocation on critical path items.

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GxP Professionals - Validation

http://www.gxppro.com/validation.html

Computer Software Validation (CSV). We can assist you with your IQ/OQ/PQ validation for your computer systems so it will meet FDA requirements and industry standards. SCADA (Supervisory Control and Data Acquisition). SAP and ERP systems. Training Systems (e.g. ComplianceWire). Electronic Document Management Systems (Documentum). Investigation Systems (TrackWise, ETQ). We can develop computer validation documents necessary to complete your validation package such as:. 21 CFR Part 11 Assessments.

5

GxP Professionals - Welcome

http://www.gxppro.com/index.html

Welcome to GXP Professionals. GxP Professionals specializes in full life cycle development of computer systems for the pharmaceutical industry. We can perform audits on your computer system validation and documentation to prepare for FDA audits. We can assess your product line and determine your process reliability. We can assist in managing your pharmaceutical IT projects from end-to-end. Contact us today for more information.

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GxP Professionals - Welcome

Welcome to GXP Professionals. GxP Professionals specializes in full life cycle development of computer systems for the pharmaceutical industry. We can perform audits on your computer system validation and documentation to prepare for FDA audits. We can assess your product line and determine your process reliability. We can assist in managing your pharmaceutical IT projects from end-to-end. Contact us today for more information.

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