Informational EU – SCHEER – Minutes of the Working Group meeting on guidelines on the benefit-risk assessment of the presence of phthalates in certain medical devic

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
M Informational EU – Minutes of the 24 July 2019 SCHEER Working Group on safety of breast implants in relation to anaplastic large cell lymphoma (BIA-ALCL) meeting Medical Device and FDA Regulations and Standards News 0
M Informational EU – Hearing on the SCHEER preliminary Guidelines on the presence of Phthalates in certain medical devices (Brussels, 04 April 2019) – Summary records Medical Device and FDA Regulations and Standards News 0
A Fire Testing - EN 50339 Not 20 minutes ISO 17025 related Discussions 0
T Quality auditor legal right to see Board meeting minutes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
S Management Review (9.3) - Management Review Minutes/Report ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
J ISO 13485 System 'soft start' - How to best reflect this in initial audits, management review minutes and other records? ISO 13485:2016 - Medical Device Quality Management Systems 3
M Informational EU – Meeting minutes – Competent Authorities on Substances of Human Origin Expert Group Medical Device and FDA Regulations and Standards News 0
L 5 minutes only for this Survey on the Value of PDCA and Your EMS Miscellaneous Environmental Standards and EMS Related Discussions 1
D Documenting Meetings through Meeting Minutes or a Form ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
D Management Review Meeting Agenda and Minutes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
D Integrated 9001, 14001, 18001 Management Review Meeting and Minutes Management Review Meetings and related Processes 10
I Content to be included or excluded in Design Control Meeting Minutes ISO 13485:2016 - Medical Device Quality Management Systems 4
D Writing Minutes (Records) from Management Review Meetings Quality Manager and Management Related Issues 11
S 45 Minutes of Lean Training to many Suppliers during a Supplier Conference Lean in Manufacturing and Service Industries 4
M Working Styles - The lazy, last minutes type Career and Occupation Discussions 13
C Example of Management Review Meeting Minutes - ISO 17025 ISO 17025 related Discussions 9
G Minutes (Records) from a Management Review Meeting Quality Management System (QMS) Manuals 4
O Should Staff be allowed to see Management Review Meeting Minutes? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
D AS 9100 Rev C "10 Minutes" Presentation to Non-Users needed AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
Sidney Vianna The last four minutes of Air France flight 447 Federal Aviation Administration (FAA) Standards and Requirements 7
K How to present the problem to your supplier General Manager in 5 minutes. Supplier Quality Assurance and other Supplier Issues 11
L Excel - calculate minutes from a start time and end time Excel .xls Spreadsheet Templates and Tools 7
S Engineering Design Review minutes as Verification & Validation Records Design and Development of Products and Processes 7
M Document Control in charge of taking Meeting Minutes? Document Control Systems, Procedures, Forms and Templates 23
Q Signature on Management Review Minutes - Quality Records ISO 13485:2016 - Medical Device Quality Management Systems 5
BradM How to Lose a Customer in 30 Minutes Coffee Break and Water Cooler Discussions 14
Z Supplier Meeting Minutes Template needed Document Control Systems, Procedures, Forms and Templates 1
E Lean Production elementary exercises (scope 45 minutes) needed Lean in Manufacturing and Service Industries 6
G Is there a requirement for Management Review Meeting Minutes? Management Review Meetings and related Processes 39
G Requirement for specified agendas and meeting minutes when documenting projects? Document Control Systems, Procedures, Forms and Templates 2
P How to convert angle measurement given in degree to degree/Minutes/Seconds? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
R Altering the Actual Date of the Management Review Meeting Minutes Management Review Meetings and related Processes 69
L Management Review Minutes and Pareto Charts Management Review Meetings and related Processes 10
M Management Review - Minutes of Meeting Management Review Meetings and related Processes 9
Marc Refusing to Show Management Review Records or Minutes Management Review Meetings and related Processes 24
N Working Voltage when high voltage flyback voltage is present IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
T Working Voltage according to 60601-1 IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
J Advice on documentation for project I am working on... ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
G Why 1 MOPP to main voltage but 2 MOPP to working voltage IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
shimonv Working with a contract manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 3
shimonv Working with a software developer who is not setup for IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 9
B 3-phase supply, overvoltage catogory, line-to-neutral and working voltage (IEC 61010-1) IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
John Broomfield Guidance on Safe Working During Covid-19 Pandemic Misc. Quality Assurance and Business Systems Related Topics 5
S Experience working with TUV SUD or Rheinland, and/or BSI Registrars and Notified Bodies 7
G Working on a Root Cause Problem Solving, Root Cause Fault and Failure Analysis 11
M Informational TGA-led IMDRF Personalised Medical Devices working group meets in Canberra Medical Device and FDA Regulations and Standards News 0
Watchcat MDD, MDR/IVDR, Working Groups, Expert Panels, MEDDEVs and Other EU Guidances EU Medical Device Regulations 32
T Is anyone working with N299.1 (Supply/service to nuclear power plants)? Various Other Specifications, Standards, and related Requirements 0
M Informational EU – 12th Meeting of the Working Group on Guidelines on benefit – risk assessment of Phthalates in Medical Devices Medical Device and FDA Regulations and Standards News 0
G Anyone working with or planning to do business in the CBD (cannabidiol) industry? US Food and Drug Administration (FDA) 1

Similar threads

Top Bottom