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| 0 | Sell | Bioterrorism Act Registration Renewal
Foreign and domestic firms that handle food and drug products, for consumption in the U.S., must revise their Bioterrorism Act ... ... products, for consumption in the U.S., must revise their Bioterrorism Act registrations by December 31st. Plans and Solutions can do the work for a VERY reasonab...
Posted on: 2014-10-13 from US - MaryLand
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| 0 | Sell | Plastic Clear Disposable Lunch Box
...anufacturing environment with GMP Clean Room and is certified by PRC State Drug Administration Bureau to manufacture packing bottles and covers for medica... ...tration Bureau to manufacture packing bottles and covers for medical use. (Registration No. 國藥包字20020256). 4. The cover liners manuf...
Posted on: 2013-10-02 from Hong Kong - Hong Kong
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| 0 | Sell | Acceptance Criteria of IVD Reagent and Registration Procedures
...stics （IVD） Reagent Registration Procedures, can be received Drug Supply Certificate and Medical Device Distribution Business License, whose... ...nd Acceptance Criteria of In Vitro Diagnostics （IVD） Reagent Registration Procedures. Each province, district or city which meets the Acceptance Cr...
Posted on: 2012-09-03 from China - Guangdong
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| 0 | Sell | The Meaning of Australian TGA registration
Australia Therapeutic Goods Administration (TGA), a federal drug authority which is subordinate to Australia Ministry of Health, provides a... ...utic goods which are consistently safe, effective and of high quality. TGA Registration carry out a range of assessment and monitoring activities to ensure therap...
Posted on: 2012-09-03 from China - Guangdong
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| 0 | Sell | Medical device registration consulting
... divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be registered according to Me... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di...
Posted on: 2012-08-13 from China - Guangdong
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| 0 | Sell | SFDA Registration Consulting
... divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be registered according to Me... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di...
Posted on: 2012-08-13 from China - Guangdong
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| 0 | Sell | Medical device SFDA Registration in China
... divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be registered according to Me... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di...
Posted on: 2012-08-13 from China - Guangdong
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| 0 | Sell | Medical device SFDA Registration in China
... divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be registered according to Me... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di...
Posted on: 2012-06-28 from China - Guangdong
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| 0 | Sell | SFDA Registration
... divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be registered according to Me... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di...
Posted on: 2012-06-08 from China - Guangdong
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| 0 | Sell | Capsules, tablets, gel, and other drug dosage forms
...cular and cerebrovascular disease, stomach and intestine disease, etc. The drugs include Doxazosin Mesylate tablets, Omeprazole enteric-coated capsules, B... ...akhstan, Venezuela, Vietnam, Thailand, Nigeria, ect. Meanwhile, the export registration work of more products is proceeding smoothly in more countries. As well, t...
Posted on: 2011-01-30 from China - Beijing
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