Revision of INMETRO Portaria 350 - August 2014

M

Marcelo

Inactive Registered Visitor
Hum, not sure exactly what you mean. It?s the revision of INMETRO Portatia 350, which defines the mandatory medical equipment certification process in Brazil.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
R Revision histories Medical Device and FDA Regulations and Standards News 1
T Minor Change vs. New Revision AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
drwallice Labeling Revision history EU Medical Device Regulations 2
A Digital Document Control - Revision ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
A If document coding is change will there be a revision Document Control Systems, Procedures, Forms and Templates 1
R What to do when revision history is too long? Misc. Quality Assurance and Business Systems Related Topics 2
M Periodically verifying revision levels of published standards Other ISO and International Standards and European Regulations 4
S Issue No. & Revision No. Document Control Systems, Procedures, Forms and Templates 4
C Requirement for Revision of Standard in all Documentation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
S Changing revision status of a reviewed document Manufacturing and Related Processes 12
M Quality Manual - Where does Revision History Section go? Document Control Systems, Procedures, Forms and Templates 8
G IATF Rules for COVID 5th revision - Re-certification audit timing IATF 16949 - Automotive Quality Systems Standard 3
B Revision 5 to IATF Coronavirus Pandemic (Covid -19) IATF 16949 - Automotive Quality Systems Standard 0
Q Version/Revision Control of CAD files Document Control Systems, Procedures, Forms and Templates 2
L Does a backdate form format can be changed if wrong revision is used? Document Control Systems, Procedures, Forms and Templates 8
B New Release of CQI-12 Coatings Process (Revision 3- Release date- 7/2020) Customer and Company Specific Requirements 2
M Gap analysis on ISO 14971:2019 with previous revision ISO 14971 - Medical Device Risk Management 12
M Is There a Revision History or Change Log for Canadian Regulations? Canada Medical Device Regulations 3
C SOP unification. Revision No, Revision history Document Control Systems, Procedures, Forms and Templates 4
I Dating controlled documents after changes - Revision History Document Control Systems, Procedures, Forms and Templates 13
I Revision History Date - date of updates or date of release? ISO 13485:2016 - Medical Device Quality Management Systems 2
J ISO 14001 revision process ISO 14001:2015 Specific Discussions 1
B CQI-11 (Plating Audit) - New revision updates IATF 16949 - Automotive Quality Systems Standard 0
P Proposed revision of IEC 62304 - 2019 IEC 62304 - Medical Device Software Life Cycle Processes 6
Sidney Vianna Interesting Discussion ISO 9001:2024 - What should be changed in the next Edition of ISO 9001? - REVISION CANCELLED May 2021 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 226
I Tracking Protoype Changes; 8D or simple document revision? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
A The latest revision number and changes in automotive core tools IATF 16949 - Automotive Quality Systems Standard 1
L Getting Notice of Revision and Accessing Public Draft Copies of ISO Standards Service Industry Specific Topics 2
A Domain of the component (EASA CM No.: CM-SWCEH-001 Issue 01 Revision 02) Point 9.3.3 (Usage domain aspects) EASA and JAA Aviation Standards and Requirements 0
M Informational ISO 14971 / ISO TR 24971 revision update – atualizações sobre a revisão Medical Device and FDA Regulations and Standards News 1
M Document Control - Revision Number in Document Names Document Control Systems, Procedures, Forms and Templates 4
L VDA 1 Documented Information and Retention (new revision 4, August 2018) VDA Standards - Germany's Automotive Standards 0
M Informational ISO TC 210 JWG 1 meeting in São Paulo – Revision of ISO 14971 and ISO TR 24971 – Medical Device Risk Management Medical Device and FDA Regulations and Standards News 0
M Revision of a Form which is a Procedure Attachment Document Control Systems, Procedures, Forms and Templates 1
S IMS Manual Review and Revision Prior to Audit ISO 14001:2015 Specific Discussions 4
2 First Article Requirements for Revision Changes of Engineering AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
ScottK Question for Auditors on 7.1.4 in the ISO9001:2015 revision ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
C Document Control - old revision vs new revision Document Control Systems, Procedures, Forms and Templates 22
R Clinical evaluation Meddev (2.7.1 revision 4) - Example or Template EU Medical Device Regulations 4
Paul Simpson Informational The role of Annex SL - High Level Structure of ISO MSS's - Revision Update February 2019 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 26
T ISO 9004:2018 Revision - Released April 2018 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
Brizilla Knowledge of the upcoming ISO 17025 Revision ISO 17025 related Discussions 5
Q Change revision number in document when only codification was changed Document Control Systems, Procedures, Forms and Templates 8
Sam Lazzara Preferred Location for Revision History Section in Documents Document Control Systems, Procedures, Forms and Templates 16
Marc When will Revision 5 of the AIAG FMEA Manual be released? FMEA and Control Plans 93
S Pre-release version of the upcoming AIAG FMEA Revision 5 FMEA and Control Plans 1
J Is there a specification that provides directions on Drawing Revision Changes Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
L Supplier Revision Confirmation of Received Engineering Documents ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M ISO 14971 and ISO TR 24971 revision ISO 14971 - Medical Device Risk Management 32
Q AS9100 Re-certification Audit - Which Revision? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3

Similar threads

Top Bottom