Zines

Zines: 1,840 results found.

March 31, 2011
Clinical Trials Advisor is devoted to helping pharmaceutical manufacturers, clinical researchers, IRBs and investigators improve clinical trial operations and GCP compliance. You'll get the latest regulatory and international news, as well as practical advice for maximizing your clinical investments. No other resource provides such valuable reporting and training applicable to every area of clinical trials. From ethics to information technology, training to patient recruitment, accreditation to disclosure — if it impacts clinical trials, CTA covers it.
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Clinical Quality Assurance Roles and Responsibilities for Auditors and Managers
Now you can learn how to FDA-proof your CQA audits … eliminate costly mistakes … and avoid FDA warning letters that say …
Cqaworkshop.com ~ Site Info Whois Trace Route RBL Check

Medical Device Risk Management An Interactive Workshop Presented by Ombu Enterprises and FDAnews
Today, it’s a bigger challenge to build, maintain and audit your risk management plan than ever before. You’ve got to act fast – and you must know what you’re doing, from A – Z. That’s why you should register today for the two-day interactive workshop Medical Device Risk Management, presented by Ombu Enterprises and FDAnews.
Deviceriskmanagement.com ~ Site Info Whois Trace Route RBL Check

Preparing for the New Global Requirements for eCTD and Regulated Product Submissions Mastering the Tools and Strategies
Paper submissions are losing traction and that's no secret. Every day regulatory authorities across the globe are turning to electronic submissions as their new preferred format ... and the FDA is leading the way. With RPS (Regulated Product Submission) poised to build on the eCTD standard, if you don't yet have your electronic submission process perfected, there's no time to lose. Many drug, biologic and device companies can already measure the difference in dollars — through increased first time acceptance rates, shorter FDA review times, and yes, speed to market.
Ectdworkshop.com ~ Site Info Whois Trace Route RBL Check

Fifth Annual FDA Inspections Summit

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Medical Device Compliance Institute 2011 Quality Design Control and Transfer Training
Register now for Medical Device Compliance Institute 2011: Quality Design Control and Transfer Training — two courses presented by EduQuest in cooperation with FDAnews that are offered separately or as an integrated three-and-a-half-day learning package — and learn how to develop a by-the-book quality management program. Leave the guessing to your competitors.
Mdcomplianceinstitute.com ~ Site Info Whois Trace Route RBL Check

April 2011
Every month you get a comprehensive briefing on the latest regulatory developments around the world, including the U.S., Europe, Latin America, Asia, Canada, Australia and more. Plus you get actual full, official English-language texts of important, hard-to-obtain proposals, regulations, rules, directives, guidances and other documents to keep you completely up-to-date on significant developments in medical device regulatory policies worldwide. Save hours on research time and overcome barriers to application approval.
Medicaldevicemonitor.com ~ Site Info Whois Trace Route RBL Check
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March 2011
Stay on top of key changes in pharmaceutical regulation around the world with this monthly resource for rules and standards flowing from the FDA, the European Medicines Agency, Health Canada, Australia's TGA, the International Conference on Harmonisation and other agencies in Europe, Japan and elsewhere. In addition to a comprehensive briefing, you get actual, full official English-language texts of important, hard-to-obtain proposals, regulations, rules, directives, guidances and other documents, to help you prepare better-documented, properly formatted drug applications for fastest processing.
Pharmaceuticalmonitor.com ~ Site Info Whois Trace Route RBL Check

Pharmaceutical Labeling Summit From FDAAA to SPL to REMS - Navigating the FDA's New Focus
This coming July, there will be an exceptional opportunity to buttonhole key FDA players plus the top lawyers, industry experts and others able to clarify new labeling requirements. Come to Washington July 22–23, 2010, when they will all be in one room, waiting to talk to you. Mark your calendar now for the Pharmaceutical Labeling Summit: From FDAAA to SPL to REMS — Navigating the FDA’s New Focus
Pharmalabelingsummit.com ~ Site Info Whois Trace Route RBL Check

PROXYNOISE - -
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Proxynoise.com ~ Site Info Whois Trace Route RBL Check