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PathWise PDF Print E-mail

4212 LaMaurice Loop
Montclair, VA 22026
Tel: 866.580.7284
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www.pathwise.com

PathWise is a training and consulting firm that works with medical device, pharmaceutical and biotechnology companies in the areas of quality and compliance. We deliver the methodology and tools to ensure compliant, effective and efficient execution of quality system requirements.
For over 15 years, we've worked with the best in the life science and manufacturing industries and bring an intimate knowledge of regulatory and compliance standards.

 
David Nettleton/Computer System Validation PDF Print E-mail

2719 Woodgate
Roseville, CA 95747
Tel:916-773-1470
Fax:916-608-4200
Email: This e-mail address is being protected from spambots. You need JavaScript enabled to view it

www.ComputerSystemValidation.com

Computer System Validation's principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, software validation, and computer system validation. He is involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications. He has completed more than 192 mission critical laboratory, clinical, and manufacturing software implementation projects.

Services include compliance related to product features, vendor audits, software validation, SOPs, training, gap analysis, remediation plans, and project management.

Projects involve: medical devices, blood bank, clinical trial, corrective action, document control, electronic data capture, Excel spreadsheets, laboratory instruments, laboratory information management (LIMS), manufacturing, enterprise resource planning, toxicology systems, and VMWare.

His latest book is "Risk Based Software Validation - Ten easy Steps" (Davis Horwood International and PDA - www.pda.org, 2006) which provides fill-in-the-blank templates for completing a COTS software validation project.

David Nettleton is the co-author of "Electronic Record Keeping; Achieving and Maintaining Compliance with 21 CFR Part 11 and 45 CFR Parts 160, 162, and 164" (Interpharm/CRC - www.crcpress.com, 2004), and "Commercial Off-the-Shelf (COTS) Software Validation for 21 CFR Part 11 Compliance" (Davis Horwood International and PDA - www.pda.org, 2003).

 

 



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