SBS - The best value in QMS software

STPi approval for laptop movement

S

smohanarangan

#1
Is it mandatory to get the STPi approval letters for laptop movement?

Did this process got changed after GST implementation?
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
D Low risk IVD study in the UK, do I need MHRA approval? UK Medical Device Regulations 0
B NIOSH Approval for Surgical N95 Respirators - Required testing US Food and Drug Administration (FDA) 2
B Document Approval Matrix Benchmarking Document Control Systems, Procedures, Forms and Templates 3
J Document Approval Signature Order Document Control Systems, Procedures, Forms and Templates 10
D Change Approval Requirements - Does every change need formal customer approval? Design and Development of Products and Processes 17
B SN95 Respirator Approval Information Other Medical Device Related Standards 0
P Notified Body Approval of Change EU Medical Device Regulations 2
Marcel DS GOST-R (Type approval for Vehicles in Russia) Other ISO and International Standards and European Regulations 0
K Joint approval between OEM and Manufacturer on Design Documents ISO 13485:2016 - Medical Device Quality Management Systems 4
O Radio modular approval in Brazil Other Medical Device Regulations World-Wide 2
O Radio Modular approval in China China Medical Device Regulations 0
dgrainger Clue to UK's new regulatory requirements - approval of all devices placed on the market? Other Medical Device Regulations World-Wide 1
was named killer AS9100 Supplier Approval Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
F How to fill out an Appearance Approval Report (AAR) APQP and PPAP 0
Q Document approval through SharePoint (without signature) Records and Data - Quality, Legal and Other Evidence 4
U Document Approval - Software company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
M Production approval testing - Alternative ideas for Validation Reliability Analysis - Predictions, Testing and Standards 4
JoCam Difference between Approval and Registration - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 2
I Can a document (form) approval record be separate? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
F Medical Devices - Hong Kong - Post approval changes regulation (China's MOH) Other Medical Device Regulations World-Wide 3
F Medical Devices-South Africa _Post approval changes and Software Other Medical Device Regulations World-Wide 0
C NB approval - Basic question about Notified Bodies and their role EU Medical Device Regulations 10
C AS9145 Appendix D PPAP Approval Form APQP and PPAP 2
N China - Start manufacturing before change approval? China Medical Device Regulations 3
I MSA requirement for 5 Micrometers + CP changes need customer approval? IATF 16949 - Automotive Quality Systems Standard 2
D ROW Approval Matrix Other Medical Device Regulations World-Wide 2
T Clinical trial - Medical device product not cleared (without FDA approval) in a drug trial Other US Medical Device Regulations 9
S Education authority requires approval of all courses - Training services provider ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Can Brazil approval be used for other countries in Latin America? Other Medical Device Regulations World-Wide 2
M Does cFDA accepts FDA approval or CE marking? China Medical Device Regulations 1
S NADCAP approval for Conventional Machining and Chemical processes - need assistance AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
DuncanGibbons FAA approval of articles (PMA, TSO) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 16
M Criteria and when to carry out Setup Approval Manufacturing and Related Processes 5
D Engineering Drawing Review and Approval Requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
K ISO 9001 Requirements for Raw Material Supplier Assessment and Approval ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
T AS9100 Maintain Approval When Business Ownership Changes AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
M Informational USFDA Guidance – Acceptance and Filing Reviews for Premarket Approval Applications (PMAs) Medical Device and FDA Regulations and Standards News 0
I Document levels and approval requirements for lower level documents like work instructions, forms etc. Document Control Systems, Procedures, Forms and Templates 18
S FDA approval process for medical device US Food and Drug Administration (FDA) 2
Sidney Vianna AS9100 News PPAP in the Aerospace Sector - What is it? AS9145 - Requirements for Advanced Product Quality Planning and Production Part Approval Process AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
D Changing Templates Approval Field Document Control Systems, Procedures, Forms and Templates 5
Q AS9120B Clause 8.4.1.1 External Providers Scope of Approval AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
J IEC 62366 - Ethical approval IEC 62366 - Medical Device Usability Engineering 5
H Informational What is PPAP (Production Part Approval Process)? APQP and PPAP 26
C Approval of raw material suppliers which do not manufacture the material ISO 13485:2016 - Medical Device Quality Management Systems 7
S MDD in 2018 - Company with no previous EU approval EU Medical Device Regulations 1
V Paint batch approval procedure for automotive industry Manufacturing and Related Processes 6
R Concessions - ISO 13485:2016 requires concession approval from customers Nonconformance and Corrective Action 2
K Where are Production parts approval specified/required? Misc. Quality Assurance and Business Systems Related Topics 2
E Approval for Templates Document Control Systems, Procedures, Forms and Templates 6

Similar threads

Top Bottom