Procedure for Handling Staff Improvement Proposals

T

Trolle

#1
Staff improvement proposals

Hello Everyone!

As Im abaout to write a procedure for handling of staff improvement proposals. I was wondering if anyone out there would care to share theire experience of this?

Cheers!
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
K Procedure for Handling of Customer Supplied Material (AS9100 Requirements) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
M Procedure for Handling Customer Return Part (Defective Part Return) IATF 16949 - Automotive Quality Systems Standard 1
Y Handling of Potentially Biohazard Material - Alcohol Cleaning Procedure ISO 13485:2016 - Medical Device Quality Management Systems 12
R Storage Procedure per NQA 1 Storage and Handling Requirements Document Control Systems, Procedures, Forms and Templates 6
K Seeking a Sample Procedure for Handling Potentially Unsafe Food Products Food Safety - ISO 22000, HACCP (21 CFR 120) 1
R Incoming Inspection, Handling and Storage Procedure for Lead Acid Batteries Other Medical Device and Orthopedic Related Topics 1
D Material Handling, Storage & Preservation Procedure for Aerospace Mechanical Parts AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
D Procedure for Preserving and Handling Flange & Pipe Materials ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
S Complaint Handling Procedure for Medical Devices 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
G Change of procedure for handling new projects - do the ongoing ones need to follow? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
A Procedure for Handling Samples needed - Failures, Retention Time, etc. Document Control Systems, Procedures, Forms and Templates 4
Ajit Basrur Anyone having procedure on "Handling Regulatory Audits" ? US Food and Drug Administration (FDA) 2
R Filter cleaning procedure for Clean Room Air Handling Unit example wanted US Food and Drug Administration (FDA) 4
Ajit Basrur Procedure for Handling Medical Customer Visits - Please review ISO 13485:2016 - Medical Device Quality Management Systems 4
B Software Validation Procedure Question - Complaint Handling Process software Software Quality Assurance 9
Le Chiffre Is a written procedure required for handling significant change? ISO 13485:2016 - Medical Device Quality Management Systems 7
J Documented procedure for handling Verbal Orders - 7.2 and Verbal Orders IATF 16949 - Automotive Quality Systems Standard 2
C Cross Function Flow Chart - Nonconformance handling procedure Document Control Systems, Procedures, Forms and Templates 7
B Procedure packs with non-medical devices EU Medical Device Regulations 1
K Need procedure for D&D inputs? ISO 13485:2016 - Medical Device Quality Management Systems 4
J Example of a defined procedure for carrying out Material Review Board (MRB) Manufacturing and Related Processes 0
A ISO 13485 procedure change and reflect to legacy manufacture items ISO 13485:2016 - Medical Device Quality Management Systems 2
S What should i choose for "testing procedure" characteristics? (N95) General Information Resources 0
S Critical characteristic on manufacturing operations test procedure Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
A SPC procedure / flow chart Statistical Analysis Tools, Techniques and SPC 2
J Action Not defined in procedure - NC - Incoming inspection AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
E Procedure ( SOP) for Device Master Record ( DMR ) and for Device History Record (DHR)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
shimonv Document Control Procedure Header Content Document Control Systems, Procedures, Forms and Templates 3
U Procedure pack components EU Medical Device Regulations 3
G Control Plan & PFMEA Review Procedure? FMEA and Control Plans 1
J Strategy for MDR Regulatory Compliance Procedure ISO 13485:2016 - Medical Device Quality Management Systems 4
A IVD in MDR procedure pack EU Medical Device Regulations 2
G RoHS Procedure REACH and RoHS Conversations 2
John Predmore Configuration Management as a process instead of a procedure AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
L How to add exemption or statement to control of document procedure? ISO 13485:2016 - Medical Device Quality Management Systems 5
A Design and development procedure for API Spec Q2 Oil and Gas Industry Standards and Regulations 6
W Using tailoring guidelines to tailor a QMS procedure ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Change management procedure when 7.3 is not applicable ISO 13485:2016 - Medical Device Quality Management Systems 5
L Sample Procedure from Contract Manufacturer Prospective ISO 14971 - Medical Device Risk Management 1
T Internal Nonconformance procedure thoughts (AS9100) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
Anonymous16-2 SOP (Standard Operating Procedure) Numbering Document Control Systems, Procedures, Forms and Templates 7
M UDI procedure/ report 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
DuncanGibbons Resources for aiding in procedure, work instruction and manufacturing plan development and management AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
S Article 22 Procedure Pack Labelling EU Medical Device Regulations 4
N EU MDR - Applicability Article 22 Systems and Procedure Packs CE Marking (Conformité Européene) / CB Scheme 4
M Example of statement for procedure pack MDR Article 22? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 0
R Procedure, Frequency and Acceptance Criteria for Replicate, Recalibration, Before-After and Intermediate Checks ISO 17025 related Discussions 8
B FDA-Medical Device Reporting (MDR )procedure compliant with 21CFR section 803 US Food and Drug Administration (FDA) 0
M MDR - Is a formal GSPR Procedure required? EU Medical Device Regulations 20
Moncia Production Planning procedure ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3

Similar threads

Top Bottom