A Chinese heparin contract testing lab has been warned by the FDA for significant cGMP violations, recalling unresolved questions and concerns from the Chinese heparin scandal a decade ago.
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Chinese Heparin Testing Lab Warned by FDA
International Pharmaceutical Regulatory Monitor
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International Pharmaceutical Regulatory Monitor (IPRM) keeps pharma professionals on top of key changes in pharmaceutical regulation around the world, covering rules and standards 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.
PLUS: in every issue, you get links to additional documents from international agencies and commissions that support IPRM’s articles, such as draft and final guidances, regulations and amendments, rules, court decisions, guidelines, procedures, explanatory notes and more.
With your subscription you’ll also receive:
- Email Alerts. Each electronic issue will be delivered right to your email inbox;
- Online Access. Search the current issue, plus 8 years of archives by keyword and relevancy;
- Free Documents. Each issue contains up to 10 links to full text of hard-to-obtain key int’l medical device regulatory references, guidances, consensus standards and industry reports, and other primary source documents you need. Never waste time tracking documents again!
- FDAnews Drug Daily Bulletin. This daily email alert brings you important FDA and international regulatory, legislative and business news in the pharmaceutical industry.
There’s absolutely no risk to you. You get our 100% Money-Back Guarantee: If at any time, for any reason, you become dissatisfied with International Pharmaceutical Regulatory Monitor, you may cancel your subscription and receive a full refund. No questions asked.
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International Pharmaceutical Regulatory Monitor (IPRM) keeps pharma professionals on top of key changes in pharmaceutical regulation around the world, covering rules and standards 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.
PLUS: in every issue, you get links to additional documents from international agencies and commissions that support IPRM’s articles, such as draft and final guidances, regulations and amendments, rules, court decisions, guidelines, procedures, explanatory notes and more.
With your subscription you’ll also receive:
- Email Alerts. Each electronic issue will be delivered right to your email inbox;
- Online Access. Search the current issue, plus 8 years of archives by keyword and relevancy;
- Free Documents. Each issue contains up to 10 links to full text of hard-to-obtain key int’l medical device regulatory references, guidances, consensus standards and industry reports, and other primary source documents you need. Never waste time tracking documents again!
- FDAnews Drug Daily Bulletin. This daily email alert brings you important FDA and international regulatory, legislative and business news in the pharmaceutical industry.
There’s absolutely no risk to you. You get our 100% Money-Back Guarantee: If at any time, for any reason, you become dissatisfied with International Pharmaceutical Regulatory Monitor, you may cancel your subscription and receive a full refund. No questions asked.
So, why wait? Become a subscriber to International Pharmaceutical Regulatory Monitor today. It couldn’t be easier.
Save $200 on One-Year Subscription to International Pharmaceutical Regulatory Monitor
International Pharmaceutical Regulatory Monitor (IPRM) keeps pharma professionals on top of key changes in pharmaceutical regulation around the world, covering rules and standards 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.
PLUS: in every issue, you get links to additional documents from international agencies and commissions that support IPRM’s articles, such as draft and final guidances, regulations and amendments, rules, court decisions, guidelines, procedures, explanatory notes and more.
With your subscription you’ll also receive:
- Email Alerts. Each electronic issue will be delivered right to your email inbox;
- Online Access. Search the current issue, plus 8 years of archives by keyword and relevancy;
- Free Documents. Each issue contains up to 10 links to full text of hard-to-obtain key int’l medical device regulatory references, guidances, consensus standards and industry reports, and other primary source documents you need. Never waste time tracking documents again!
- FDAnews Drug Daily Bulletin. This daily email alert brings you important FDA and international regulatory, legislative and business news in the pharmaceutical industry.
There’s absolutely no risk to you. You get our 100% Money-Back Guarantee: If at any time, for any reason, you become dissatisfied with International Pharmaceutical Regulatory Monitor, you may cancel your subscription and receive a full refund. No questions asked.
So, why wait? Become a subscriber to International Pharmaceutical Regulatory Monitor today. It couldn’t be easier.