The Brazilian monitoring authority ANVISA is definitely known in Europe. Of course, these authorities have their own GMP inspection. Today’s focus is on the Brazilian GMP guidelines of ANVISA. We notice a significant increase of ANVISA inspections over the recent years. South South Cooperation: the experience of ANVISA in the Aligned with the guidelines of the Brazilian Health . France (AFSSAPS) – GMP inspections.

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Problems with a contract manufacturer or lab can emerge in dozens of unexpected places, from changes in personnel or equipment to faulty SOPs and training, the list can seem impossible to tame.

For this reason we offer you more information about the Brazilian GMP guidelines. Health regulation actions in services for outpatient care routine or emergency and hospitalization; diagnostic support and therapeutic services that entail the incorporation of new technologies.

English – Anvisa

Please click here, if the newsletter is not displayed correctly. They can sign up here Market authorization for products prior to its manufacturing, market exposure or delivery to consumers. This new step-by-step guide will walk you through an in-depth topic analysis of managing contractors.

Click aanvisa to see them all With one click you get free access to our feature: Managing Contract Manufacturers and Testing Labs. Coordination of special programmes to monitor the quality of regulated products and services.

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Click here to get information about the International Certificate of Vaccination or Prophylaxis and about travelling with controlled substances. Contact Us Please use giidelines available form to contact the technical areas of Anvisa about any doubts you might have, information you wish from the Agency or to forward suggestions and complaints.

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Brazil’s GMP Guideline Available in English – ECA Academy

It combines theory and practice in an ideal way and is used in over 70 countries around the world. The EMA has published a draft guideline on similar biological medicinal products on May 2,which is now open for public consultation.

Please use the available form to contact the technical areas of Anvisa about any doubts you might have, information you wish from the Agency or to forward suggestions and complaints.

Voltar para o topo! Draft Guideline on Biosimilars The EMA has published a ggmp guideline on similar biological medicinal products on May 2,which is now open for public consultation.

Draft Guideline on Biosimilars. Our feature provides a brief insight into these guidelines. You receive this newsletter because you have previously registered anvia www. Exporting to Brazil Click here to learn more about border controls performed in Brazil for imported products regulated by Anvisa.

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Pharmaceutical Regulatory Affairs: Open Access

Dear Colleagues, a lot of manufacturers of medicinal drug products have to fulfill a variety of different GMP regulations. If you need support to organize your contract manufacturers in an efficient way – please read more our new publication “Managing Contract Manufacturers”. Click here to learn more about border controls avnisa in Brazil for imported products regulated by Anvisa.

Managing Contract Manufacturers Problems with a contract manufacturer or lab can emerge in dozens of unexpected places, from changes in personnel or equipment to faulty SOPs and training, the list can seem impossible to tame. Please write your questions preferably in Portuguese, English or Spanish.

Control of the import, export and circulation of ingredients and goods subject to health regulation. Travellers Click here to get information about the International Certificate of Vaccination or Prophylaxis and about travelling with controlled substances. Don’t reinvent the wheel and save time and money.

Adoption of preemptive and control measures for outbreaks, epidemics and public health emergencies. This step-by-step guide will walk you through an analysis program.