Informational ANVISA – Aberta inscrição para evento sobre dispositivos médicos (ANVISA medical devices day event)

You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
Y Gap assessment comparing RDC ANVISA 665/2022 and RDC ANVISA 16/2013? Other Medical Device Related Standards 0
kys123 Implications of failing an Anvisa Audit for ISO 13485 Certification ISO 13485:2016 - Medical Device Quality Management Systems 4
P Brazil - ANVISA - distance selling Other Medical Device Regulations World-Wide 0
L ANVISA’s RDC 665 replaces previous regulations including RDC 16/2013 and IN 08/2013, and comes into effect on May 2, 2022 Other Medical Device Regulations World-Wide 2
L Clinical research - Request from ANVISA ISO 14971 - Medical Device Risk Management 1
K ANVISA B-GMP Auditing requirements for Contract Manufacturers Other Medical Device Regulations World-Wide 1
M Informational ANVISA – CONSULTA PÚBLICA Nº 734, DE 22 DE OUTUBRO DE 2019 – Registro de dispositivos médicos para diagnóstico in vitro (in vitro diagnostic medical m Medical Device and FDA Regulations and Standards News 0
M Informational ANVISA – CONSULTA PÚBLICA No 730, DE 14 DE OUTUBRO DE 2019 – Registro de dispositivos médicos (Public consultation – registration of medical devices) Medical Device and FDA Regulations and Standards News 0
M Informational ANVISA regulation for personalized/custom medical devices – RESOLUÇÃO – RDC Nº 305, DE 24 DE SETEMBRO DE 2019 Medical Device and FDA Regulations and Standards News 0
M Informational ANVISA – NOTA TÉCNICA 001/2019/GEMAT/GGTPS/ANVISA – Assuntos de Petições da Gerência de Tecnologia de Materiais de Uso em Saúde Medical Device and FDA Regulations and Standards News 0
B MDSAP 8.2.6 CH6 task 17 ANVISA 16/2013 3.2.1 - Label History in Device history record Other Medical Device Regulations World-Wide 3
M Informational ANVISA – INSTRUÇÃO NORMATIVA N° 32, DE 12 DE ABRIL DE 2019 – Delegação da inspeção para verificação das Boas Práticas de Fabricação – Delegation of in Medical Device and FDA Regulations and Standards News 0
A How should the Medical Device OEMs be declared to ANVISA? Other Medical Device Regulations World-Wide 0
M Informational ANVISA – Notification for Class 1 devices – Resolução da Diretoria Colegiada – RDC nº 270 de 28/02/2019 Medical Device and FDA Regulations and Standards News 0
M Medical Device News Disponibilizados textos das CPs 584, 585 e 585 da ANVISA Medical Device and FDA Regulations and Standards News 0
M Medical Device News ANVISA – Consulta Pública nº 586 de 20/12/2018 – Diretrizes de Garantia da Qualidade para Validação, Monitoramento e Controle de Rotina dos Processos Medical Device and FDA Regulations and Standards News 0
M Medical Device News ANVISA – Consulta Pública nº 585 de 20/12/2018 – Boas Práticas para o Processamento de Produtos utilizados na assistência à saúde Medical Device and FDA Regulations and Standards News 0
M Medical Device News ANVISA – Consulta Pública nº 584 de 20/12/2018 – Enquadramento de dispositivo médico como de uso único ou reutilizável Medical Device and FDA Regulations and Standards News 0
M Medical Device News New ANVISA health services public consultations – Consultas públicas de serviços em saúde Medical Device and FDA Regulations and Standards News 0
L ANVISA RDC 16 - purchasing records Other Medical Device Regulations World-Wide 2
R Are the ISO Standards actually required for health product registration on ANVISA? Other Medical Device Regulations World-Wide 4
pittmatj Brazil - Electronic Registration with ANVISA Other Medical Device Regulations World-Wide 10
S Is ANVISA site certification not required for Class I and II devices ? Other Medical Device Regulations World-Wide 1
L Reporting changes to ANVISA Other Medical Device Regulations World-Wide 24
B Brazil ANVISA Medical Device Labeling/IFU Requirements Other Medical Device Regulations World-Wide 1
pittmatj ANVISA Import Permit for Brazilian Customs Other Medical Device Regulations World-Wide 1
O List of ANVISA Registered Companies Other Medical Device Regulations World-Wide 1
O Implementation of GMP - Technical files for ANVISA Registration Other Medical Device Regulations World-Wide 3
M Informational Medical Device Registration Process in Brazil - Anvisa (Part 3) Other Medical Device Regulations World-Wide 134
K Would ANVISA (Brazil) inspect our new manufacturing site? Other Medical Device Regulations World-Wide 12
AnaMariaVR2 ANVISA Considers Accepting Foreign GMP Certifications US Food and Drug Administration (FDA) 0
B ANVISA B-GMP Inspection Schedule Other Medical Device Regulations World-Wide 4
Ajit Basrur Statement of Cooperation Among FDA - TGA - ANVISA - HPFB 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
M Medical Device Registration Process in Brazil - Anvisa (Part 2) Other Medical Device Regulations World-Wide 71
AnaMariaVR2 ANVISA Strike to Delay Medical Device Reviews in Brazil Other Medical Device Regulations World-Wide 2
S Anvisa & INMETRO - Registering Non-Electrical Medical Devices in Brazil Other Medical Device Regulations World-Wide 2
P IVD Classification in Brazil and Anvisa Guidance Other Medical Device Regulations World-Wide 10
M Future revision of ANVISA RDC 59 - Brazilian GMP Other Medical Device Regulations World-Wide 14
C Anvisa Manufacturer Audit - Product produced at two different Sites Other Medical Device Regulations World-Wide 3
E Cross Reference Matrix for TGA and ANVISA requirements Other Medical Device Regulations World-Wide 3
R Medical Device Approval in Brazil - Understanding INMETRO and ANVISA Other Medical Device Regulations World-Wide 127
B IVD ANVISA Registration Process in Brazil and Registration Change Other Medical Device Regulations World-Wide 11
R Registering Medical Device in Brazil ANVISA - Fee Structure Other Medical Device Regulations World-Wide 1
S Who pays Brazil ANVISA Inspection Fees Other Medical Device Regulations World-Wide 38
S ANVISA Audit by 3rd Party? Other Medical Device Regulations World-Wide 4
A Material Grade Change Notification to Brazil ANVISA Other Medical Device Regulations World-Wide 2
Mikilk B-GMP Audit (Anvisa Brazil) - Checklist in English or other useful documents wanted Other Medical Device Regulations World-Wide 6
N ANVISA Inspection / Audit - French Company - China Manufacturing - Brazil Distributor Other Medical Device Regulations World-Wide 7
M ISO 14971 becomes mandatory in Brazil - ANVISA Normative Instruction 13/2009 ISO 14971 - Medical Device Risk Management 23
M Medical Device Registration Process in Brazil - Anvisa (Part 1) Other Medical Device Regulations World-Wide 301

Similar threads

Top Bottom