Examples of using Anvisa in English and their translations into German
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Colloquial
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Official
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Ecclesiastic
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Medicine
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
ANVISA recognises MDSAP audits as initial audits.
This institution is comparable to the US Food and Drug Administration or the ANVISA in Brazil.
Brazil's ANVISA sets institutional performance goals.
Since December 2016 Leisegang colposcopes are registered at ANVISA, the Brazilian Health Regulatory Agency.
ANVISA medical device registration consulting.
The Brazilian Ministry of Health, ANVISA has approved the sales of Sativex, a drug derived from cannabis.
ANVISA launches health products monitoring programme.
Manufacturer of medical devices, who wants to put products into circulation in Brazil,has to be registered with ANVISA.
ANVISA registration consulting for medical device companies.
Confidential audit information shared based on agreements between ANVISA and other medical device market regulators.
Brazil: ANVISA plans to propose the addition of'systems' to IN 03/2015.
The National Health Surveillance Agency(in Portuguese,Agência Nacional de Vigilância Sanitária, ANVISA) is a regulatory body of the Brazilian government.
ANVISA holds consultation on labelling for medical devices containing natural rubber latex.
All supplements, cosmetics, vitamins,homeopathic, and other health care products must be registered with the Federal Sanitation Agency ANVISA.
ANVISA has always permitted the import of medical cannabis and hemp oil for the treatment of cancer and Parkinson's disease in individual cases.
After several lawsuits filed by patients who asked toreceive a cannabis based treatment in Brazil, ANVISA has eased its rules in the recent years.
ANVISA has evaluated Endosulfan and has come to the conclusion that it is dangerous for humans and the environment and that it should be forbidden.
Emergo will provide updates as they become available on any potential newregulation as well as how existing ANVISA Class I registrants will be affected.
ANVISA, the US Food and Drug Administration, Health Canada, Japan's Pharmaceutical and Medical Devices Agency and the Australian Therapeutic Goods Administration.
And while Health Canada and the FDA are continuing to actively support the program, other actions,particularly those of ANVISA, are not giving manufacturers enough incentive to participate.
Brazil's ANVISA has published a new regulation to clarify changes to its Brazil GMP inspection and certification process.
Copy of a GoodManufacturing Practice inspection or audit report issued by the regulator overseeing the manufacturer's country of origin, or by an auditing organization accredited by ANVISA.
ANVISA, CFDA and Roszdravnadzor update and release regulations on a much more frequent basis than the established regulatory authorities, causing turmoil in the industry and lack of trust.
The drug in question, nick-named“three in one“is a combination of tenofovir, lamivudine and efavirenz, a mix whichis still awaiting authorisation by the National Health Surveillance Agency Anvisa.
Local regulations such as the Food Safety Modernization Act(FSMA)in the USA, ANVISA in Brazil, and the Food Standards Act in Europe also play a key role in ensuring food produced is safe for consumers.
Before medical device manufacturers can legally sell their products in Brazil, they must comply with Brazilian medical device regulationsset forth by the Agência Nacional de Vigilância Sanitária ANVISA.
Instead, ANVISA has proposed establishing a notification system whereby a manufacturer's Brazilian Registration Holder(BRH) would electronically submit a minimal amount of information to the agency, with no technical analysis performed.
Higher fees allow ANVISA, CFDA and Roszdravnadzor to hire additional staff and add resources to speed up device review processes, for example, and relieve"bottlenecks" resulting from too few or ill-trained regulatory staff having to process high volumes of market authorization applications.
