PMP Gateway systems - Looking for a robust automotive gateway system

R

rskeins

#1
#1
I am looking for a robust automotive gateway system that has checklists for each phase as well review presentations/deliverables
 
SQCpack - Communicate Quality Metrics
Elsmar Forum Sponsor
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
L PMP Project Management and APQP - Differences APQP and PPAP 9
S Parts, Materials and Processes (PMP) Control Plan - Mil-Std-3018 Misc. Quality Assurance and Business Systems Related Topics 1
S GM PMP characteristics on a GM print next to the gage points Customer and Company Specific Requirements 2
S FDA electronic submission gateway (ESG): FAILED eMDR Submission Other US Medical Device Regulations 3
A Basic UDI and UDI-DI for hip implant systems EU Medical Device Regulations 0
J Keyence Measurement Systems General Measurement Device and Calibration Topics 3
T Add checking aid to quality systems Manufacturing and Related Processes 2
J Elsmar Ownership - PQ Systems Forum News and General Information 2
Le Chiffre Online training available for ISO/IEC 17021-1: Requirements for bodies providing audit and certification of management systems Training - Internal, External, Online and Distance Learning 3
Sidney Vianna Release of ISO 10013:2021, Quality management systems – Guidance for documented information Other ISO and International Standards and European Regulations 0
optomist1 How Secure Are Our Software Systems Software Quality Assurance 7
C Barcode Labelling - Mistake Proofing Ideas & Systems Manufacturing and Related Processes 2
P IQ, OQ, PQ protocol, and report templates for Distributed Control Systems in Pharmaceutical Manufacturing Systems. Qualification and Validation (including 21 CFR Part 11) 0
S User evaluation for self monitoring blood glucose test systems US Food and Drug Administration (FDA) 4
S Manufacturing Execution Systems Software Costs Manufacturing and Related Processes 0
Ajit Basrur FDA News Harmonizing and Modernizing Regulation of Medical Device Quality Systems (7-2020) US Food and Drug Administration (FDA) 13
R Requirements for MDR Article 22 Systems EU Medical Device Regulations 1
N EU MDR - Applicability Article 22 Systems and Procedure Packs CE Marking (Conformité Européene) / CB Scheme 4
K Best Measurement Systems Demos in California? General Measurement Device and Calibration Topics 1
Bev D Verification and Validation of Measurement Systems Misc. Quality Assurance and Business Systems Related Topics 0
M Risk and Corrective actions - Currently no FMEA's - Car systems Risk Management Principles and Generic Guidelines 8
R MDR Article 22: Systems and procedure packs Other Medical Device Regulations World-Wide 12
M Informational US FDA Final Guidance – Intravascular Catheters, Wires, and Delivery Systems with Lubricious Coatings – Labeling Considerations Medical Device and FDA Regulations and Standards News 0
D Why are pharma companies automating QMS systems? Quality Management System (QMS) Manuals 2
Ajit Basrur FDA News Harmonizing and Modernizing Regulation of Medical Device Quality Systems US Food and Drug Administration (FDA) 18
M Informational TGA Consultation: Proposed clarification of the regulatory requirements for medical device systems and procedure packs Medical Device and FDA Regulations and Standards News 2
M Different procedure templates for different standards - We have two different management systems ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
H Question about implications of performing Firmware upgrade via MDDS - Medical Device Data Systems 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
M Routine testing of medical electrical systems - What specific electrical safety tests should be performed? IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
M Informational US FDA final guidance – Marketing Clearance of Diagnostic Ultrasound Systems and Transducers Medical Device and FDA Regulations and Standards News 0
M Informational TGA – Guidance on Therapeutic Goods (Conformity Assessment Standard for Quality Management Systems) Order 2019 Medical Device and FDA Regulations and Standards News 0
J Is Design Validation required for fixtures or test systems used to manufacture a product? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
R Timeframe for IATF 16949 certification to accumulate evidence of conformance of systems? IATF 16949 - Automotive Quality Systems Standard 2
M How to calculate benefits? Moving some developed non controlled software/automation systems Service Industry Specific Topics 2
Z Security for Approvals - Cloud based Complaint, NC, and CAPA systems Qualification and Validation (including 21 CFR Part 11) 8
N EU MDR Basic UDI-DI and Technical Documentation for Systems EU Medical Device Regulations 22
pbojsen Computerized Learning Management Systems (Training systems) recommendations? ISO 13485:2016 - Medical Device Quality Management Systems 3
Sidney Vianna Safety Management Systems - SM-0001 Standard for Aviation Organizations AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
M Interview question - IMS (Integrated Management Systems) a necessity or an ISO mistake? ISO 14001:2015 Specific Discussions 10
AnaMariaVR2 Pharmaceuticals News Transdermal and Topical Delivery Systems: FDA & EMA Guidance US Food and Drug Administration (FDA) 0
M Training to help Familiarize myself to the Standards and the way these systems work AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
pbojsen Intuitive Quality Design and Documentation Systems ISO 13485:2016 - Medical Device Quality Management Systems 12
D Use of password managers on validated computer systems (21 CFR Part 11) Medical Information Technology, Medical Software and Health Informatics 2
ScottK What Became of Alamo Consulting or Alamo Learning Systems Consultants and Consulting 5
R Custom Records and Quality Systems - Products that change frequently Other US Medical Device Regulations 3
W ISO 14155 - Electronic clinical data systems - Definition Other Medical Device Related Standards 0
B NEED HSE-MS Gap Analysis between 2 existing Management Systems Occupational Health & Safety Management Standards 0
Q Practical guide to scan for Risks in all QMS systems without missing any ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
B Records Destroyed - Hurricane Harvey has likely destroyed our Quality Systems Records Records and Data - Quality, Legal and Other Evidence 10
U CE Marking of Customized Ruggedised Computer Systems Solutions CE Marking (Conformité Européene) / CB Scheme 5

Similar threads

Top Bottom