qlaunch.com
Who is QLaunch? - QLaunch
http://www.qlaunch.com/who-is-qlaunch.html
QLaunch is a service of QPharma. A 20-year leader in the delivery of regulatory compliance and commercial solutions to pharmaceutical, medical device, and other life sciences companies. The division was founded based on QPharma's vast experience working with life sciences brand and regulatory teams at nearly all stages of the product life cycle. Peter Shaw, M.D. Trade; Software as a Service (SaaS) solution. Python’s suite of solutions, ranging from sample accountability services to training/lea...Ed has ...
cadencemc.com
Global Solution Providers – Cadence Management Corporation
http://www.cadencemc.com/global-solution-providers-2
Toll Free: 1.800.448.0173 Int'l 1.503.CADENCE (223.3623). Organizational Project Management (OPM) Courses. Project Management: A Practical And Adaptive Methodology For Getting Projects Done. Program Management: A Means to Manage Complexity. Portfolio Management: A Practical Guide for Executives and Managers. Managing Project Management: Skills for Cross-Functional Project Success. Executive Briefing: Project Management. Executive Briefing: Portfolio & Program Management. Specific Focus Training Courses.
print-tech.biz
Print Tech, The Future of Printing
http://www.print-tech.biz/links/index.html
National Association of Print Leaders. New Jersey Chamber of Commerce. Association for Corporate Growth. Http:/ chapters.acg.org/newjersey. Executives Association of New Jersey. Jersey Shore Public Relations and Advertising Assoc. The Gateway Chamber/Irish Business Assoc. New Jersey Society of Association Executives. Newark Regional Business Partnership.
qlaunch.com
What is QLaunch? - QLaunch
http://www.qlaunch.com/what-is-qlaunch.html
Before and After Launch, We've Got You Covered. We Guarantee the Process. No one can guarantee that a product will be approved to go to market, or that the product will be a blockbuster — but by applying the QLaunch methodology, life sciences firms are guaranteed. To follow the appropriate legal, regulatory, and commercial steps necessary to position a product for launch and success in the marketplace. QLaunch is a service of QPharma.
validationandregulatorycompliance.blogspot.com
Validation and Regulatory Compliance for Life Science Professionals: February 2011
http://validationandregulatorycompliance.blogspot.com/2011_02_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. Monday, February 28, 2011. New FDA Regulation for Medical Device Data Systems (MDDS). Written By Elise Miner - Validation Manager, QPharma. The electronic transfer or exchange of medical device data from a medical device, without altering the function or parameters of any connected devices. But the changes the FDA are making to the MDDS rule affect bo...
validationandregulatorycompliance.blogspot.com
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 ...
validationandregulatorycompliance.blogspot.com
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...
validationandregulatorycompliance.blogspot.com
Validation and Regulatory Compliance for Life Science Professionals: April 2011
http://validationandregulatorycompliance.blogspot.com/2011_04_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. 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? Tuesday, April 19, 2011. Written by Paul Melamud - Validation Manager, QPharma. ANSWERING THE QUESTION – HOW FDA REGULATES THIS PRODUCT. The question posed at the start of thi...
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...
validationandregulatorycompliance.blogspot.com
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...