QPharma is a Regulatory Compliance and Validation consulting firm that caters to the life science industry.
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Validation and Regulatory Compliance for Life Science Professionals | validationandregulatorycompliance.blogspot.com Reviews
https://validationandregulatorycompliance.blogspot.com
QPharma is a Regulatory Compliance and Validation consulting firm that caters to the life science industry.
validationandregulatorycompliance.blogspot.com
Validation and Regulatory Compliance for Life Science Professionals: Understanding both Electronic and Handwritten Signatures within the Context of Part 11
http://validationandregulatorycompliance.blogspot.com/2010/06/understanding-both-electronic-and.html
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Wednesday, June 2, 2010. Understanding both Electronic and Handwritten Signatures within the Context of Part 11. Written by Robert Finamore - Director, Validation Services. 21 CFR Part 11; Electronic Records, Electronic Signatures. To discuss this topic further, contact Rob at mailto:robert.finamore@qpharmacorp.com. Labels: 21 CFR Part 11. Understandi...
Validation and Regulatory Compliance for Life Science Professionals: November 2010
http://validationandregulatorycompliance.blogspot.com/2010_11_01_archive.html
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Tuesday, November 23, 2010. Don't Miss Our End of Year Events! Will you be attending any of these events? We hope you will be joining our Subject Matter Experts as they share their insight and expertise on some of the most pressing issues before the close of the year! IPA'S Good Laboratory Practices. BIOCOM Presents: Off Label Promotion. FDA guidance ...
Validation and Regulatory Compliance for Life Science Professionals: A Practical Guide to Handling Product Complaints
http://validationandregulatorycompliance.blogspot.com/2011/02/practical-guide-to-handling-product.html
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Tuesday, February 1, 2011. A Practical Guide to Handling Product Complaints. Written by Zina Bulbuc - Validation Engineer, QPharma. Complaints, complaints, complaints…. Everybody gets them: from friends and family members, from customers and business partners, from bosses and co-workers. How do we handle them to keep everybody happy? Second, it has to...
Validation and Regulatory Compliance for Life Science Professionals: Don't Worry…After All, What Can FDA Do to Us?
http://validationandregulatorycompliance.blogspot.com/2011/05/dont-worryafter-all-what-can-fda-do-to.html
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Monday, May 16, 2011. Don't Worry…After All, What Can FDA Do to Us? Written By: Jeff Boatman - CQA, Senior Subject Matter Expert, Quality Systems, QPharma. Quite a lot, actually! 1 Greasing the Skids. 2 The “Guidance” Document that's Anything But. A similar and more general guidance is the one for Part 11. On many of my audits, I’ve made obs...Until y...
Validation and Regulatory Compliance for Life Science Professionals: What’s The Deal with McNeil’s Consent Decree?
http://validationandregulatorycompliance.blogspot.com/2011/04/whats-deal-with-mcneils-consent-decree.html
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Monday, April 25, 2011. What’s The Deal with McNeil’s Consent Decree? Written by Clinton Ballard - Validation Specialist, QPharma. Johnson and Johnson McNeil. What do you think? Subscribe to: Post Comments (Atom). There was an error in this gadget. And why are we blogging? Morristown, NJ, United States. View my complete profile. Best Practices for Val...
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CAD Data Validation & Checking | Theorem Solutions CAD Validation and Checking Resource
CAD Data Validation and Checking. Theorem Solutions CAD Validation and Checking Resource. Theorem Solutions is a world leader in the field of Engineering Data Services and Solutions. This leadership position stems from the quality of our technology and the people in the company. Quality comes not only from the skills and commitment of our staff, but also from the vigorous industrial use of our technology and services by world leading customers. Leave a Reply Cancel reply. Enter your comment here. You are...
validationandregulatorycompliance.blogspot.com
Validation and Regulatory Compliance for Life Science Professionals
Validation and Regulatory Compliance for Life Science Professionals. Actionable Intelligence for the Life Science Industry. Keep us On Your Radar with RSS. Tuesday, May 8, 2012. Establishing Quality Systems: The Importance of Partnership. Written by Dawn Gabriel, Ph.D., Director of Quality and Compliance, QPharma. What do you think? Tuesday, February 21, 2012. Selecting an Alternative Sampling Provider: Considerations for Brand Managers. Written by Michael Milunec, Director of Operations, QPharma. The in...
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Project Hosting for Open Source Software. By clicking Delete, all history, comments and attachments for this page will be deleted and cannot be restored. Change History (all pages). ValidationAspects provides State and Interception validation on .net Objects, Properties and Method Parameters. Validation can be declared via attributes and/or augmented/replaced with validation functions at runtime. Supports asp.net MVC, WPF, Silverlight, PostSharp, and Unity. Real-time augmentation / replacement. Intercept...
Validation Associates | Homepage
Welcome To Validation Associates. Validation Projects and/or Staffing, Clinical Systems Risk Assessment, Validation Project Management, 21 CFR Part 11, Test Script Creation. Compliance and Quality System. Consultation, Regulatory Gap Analysis, Program Development, GMP/QSR, FDA Readiness Audit, Planning, Implementation and Training. GLP Assessments, GCP Compliance Assessments, Clinical Investigator, Sponsor, Monitor, Central Study File, Database and Data Mgmt. Deviation and Document management. Validation...
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