Deadline Extension? New Excuse? Computer Enhancers for everyone

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D Corrective Action Timing - IATF CB Deadline IATF 16949 - Automotive Quality Systems Standard 2
E Brexit UK MDR brexit out of sync with EU MDR deadline? UK Medical Device Regulations 4
T Rumours that class 1 NS, NM, NR devices will have a new deadline for MDR compliance EU Medical Device Regulations 3
M Informational BSI – ISO 13485 and products with May 2020 deadline for MDR certification Medical Device and FDA Regulations and Standards News 0
JoshuaFroud CE Marking and Brexit - Product shipped to a distributor prior to the March deadline EU Medical Device Regulations 2
O IEC 60601-1-2 4th edition transition deadline Dec 31 2018 CE Marking (Conformité Européene) / CB Scheme 1
Sidney Vianna One year to ISO 9001 and 14001 transition deadline. ISO & IAF communique' ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
Sidney Vianna IATF bringing stakeholders together to ensure Transition by the 2018-09-14 deadline IATF 16949 - Automotive Quality Systems Standard 10
C Recurring Nonconformance - Missing Deadline for Closing a Corrective Action Problem Solving, Root Cause Fault and Failure Analysis 14
P FDA's deadline for IEC 60601-1 3.1 edition compliance - Aug 1, 2016 IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
Scott Catron OSHA Hazcom GHS Implementation - June 1 2015 deadline Occupational Health & Safety Management Standards 8
N Clarification on Canada's ESDM's and ECA's and the February deadline Miscellaneous Environmental Standards and EMS Related Discussions 7
Sidney Vianna AS91X0 Transition Deadline - New IAQG Decision - 2012 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 54
G IVD EU Notifications - May 2011 deadline for mandatory use of the Eudamed database EU Medical Device Regulations 7
T ISO 9001:2008 Recertification Audit Deadline ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
S Deadline for complying/replying to a Customer Complaint Customer Complaints 6
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C What can I do if I cannot meet PPAP deadline? APQP and PPAP 4
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Q RAB 17024 & New Coke! RABQSA Suspends 17024 Transition Deadline ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 8
F Multi-Level CA (corrective action) Process? Levels of investigation, reply deadline Nonconformance and Corrective Action 4
R What is the transition deadline for ISO 13485:2003? ISO 13485:2016 - Medical Device Quality Management Systems 4
C Consequences of Missing the Chrysler July 1st TS 16949 Deadline IATF 16949 - Automotive Quality Systems Standard 31
Claes Gefvenberg Past the deadline: Your 9001:2000 status? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 38
H December Deadline - Registrars can not maintain certifications after December? Registrars and Notified Bodies 48
S Confused about the TS 16949 Deadline - Presumably a Big 3 mandate? IATF 16949 - Automotive Quality Systems Standard 4
B EU MDR transitional period extension EU Medical Device Regulations 4
S Class1device - MDD extension EU Medical Device Regulations 2
A MDD Extension - certificate expiry CE Marking (Conformité Européene) / CB Scheme 4
G Epo-tek 301 shelf life extension Other Medical Device and Orthopedic Related Topics 0
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N Class III PMA shelf life extension US Medical Device Regulations 2
W AS9100 Shelf Life Extension or Exemption AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
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B IATF 16949 News Six month extension on all valid IATF 16949 certs IATF 16949 - Automotive Quality Systems Standard 10
J UCLA extension Medical Device Engineering Program Training - Internal, External, Online and Distance Learning 0
J Documenting a Calibration Interval Extension Calibration Frequency (Interval) 7
J Remote location vs. site extension IATF 16949 - Automotive Quality Systems Standard 3
R Extension of product nonconformances - Construction project Nonconformance and Corrective Action 7
R Documenting Expiration Date Extension for a specific lot ISO 13485:2016 - Medical Device Quality Management Systems 12
M FDA News USFDA Proposes to End Temporary Extension of GUDID’s Grace Period Medical Device and FDA Regulations and Standards News 3
J ISO 13485 Recertification audit extension ISO 13485:2016 - Medical Device Quality Management Systems 1
F Extension of a stability study for an API Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
B Site Extension across the street to expand IATF 16949 - Automotive Quality Systems Standard 4
I Device Shelf Life Extension to 48 months without involving the FDA 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
G Is ISO/TS16949 Extension Available? IATF 16949 - Automotive Quality Systems Standard 3
D Ethylene Oxide Sterile Implantable Medical Device Shelf Life Extension Other Medical Device Related Standards 1
M TS 16949 Site Extension Elimination? IATF 16949 - Automotive Quality Systems Standard 7

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