Statutory/Regulatory for NACE Code 25.9 (Manufacture of fabricated metal products)

You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
pcoltsqe AS9100 - The statement 'applicable statutory and regulatory requirements' AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
Q IATF 16949 Cl. 4.4.1.1, 8.4.2.2, 8.6.5 - Statutory and Regulatory Requirements IATF 16949 - Automotive Quality Systems Standard 6
apestate How to determine all regulatory and statutory requirements to be met? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
S AS9100 Foreword: Meet or Exceed customer & applicable statutory and regulatory req... AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 7
D What is difference between Statutory and Regulatory with Documents of External Origin ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
G AS9100 - Clarify what is meant by Statutory & Regulatory Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
M 7.4.1.1 Statutory & Regulatory Conformity: Legal Requirements of which Country? IATF 16949 - Automotive Quality Systems Standard 4
M AS9100 4.1 How can I know/monitor applicable regulatory/statutory requirements? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
somashekar About ISO9001 Scope and Applicable Statutory and Regulatory Requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
R Customer, Statutory and Regulatory Requirements - Intent of Clause 4.1, Note 3 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
V Statutory & Regulatory Requirements - Who is accountable for changes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
S What Statutory & Regulatory Requirements can an ISO 9001 internal auditor audit Internal Auditing 15
J Any other statutory & regulatory requirements other than FAA Federal Aviation Administration (FAA) Standards and Requirements 4
J Internal Auditing Requirements of Statutory and Regulatory Requirements for AS9100 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 14
N Statutory and regulatory requirement examples in metal fabrication Various Other Specifications, Standards, and related Requirements 8
B Statutory vs. Regulatory requirements - ISO 9001:2008, clause 1.1 Note 2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
V Statutory and regulatory requirements (7.2.1c) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
somashekar Cl 7.2.1c Statutory and Regulatory Requirements Related to the Product ISO 13485:2016 - Medical Device Quality Management Systems 4
K Please define "Statutory and Regulatory Requirements" ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
W Statutory and Regulatory requirements - Including Shipping ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
R Statutory Requirements - 7.3.2 - Applicable statutory and regulatory requirements IATF 16949 - Automotive Quality Systems Standard 1
I Statutory and Regulatory Requirements - How to address 7.2.1c ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
A At what stage do you review new product statutory / regulatory requirements? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
A Where can we find Statutory and Regulatory Requirements related to our Product? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
Marc Statutory & Regulatory Requirements - Comply with applicable laws - 7.2.1 (c) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
V Updating Quality Manual - Adding the word Statutory in front of laws and regulations Quality Management System (QMS) Manuals 3
G ISO9001 applicable statutory requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
J Determining Legal& Statutory requirements while Auditing Design & Development process Design and Development of Products and Processes 8
A ISO 13485 CERTIFICATION WITH REGULATORY ISO 13485:2016 - Medical Device Quality Management Systems 1
B Regulatory Reference for Controlled Drug Manufacturer Supplier Quality Assurance and other Supplier Issues 0
D FDA combo product-need to define direct & indirect impact regarding safety,quality & regulatory.Can anyone point me in right direction-SupplierMgmt 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
Leigh76 Regulatory Path for Providing Sterile Product in Bulk Non-Sterile Form to Kit Packers US Medical Device Regulations 3
D Regulatory consultant with experience in auto injectables US Food and Drug Administration (FDA) 0
C MSc Dissertation Survey - Regulatory Approval Medical Device and FDA Regulations and Standards News 1
V Regulatory consultants for US FDA ANDA - pharma / drug products Consultants and Consulting 0
V Countries without Formal Regulatory Approval Process Other Medical Device Regulations World-Wide 0
P Crucial Suppliers Listed on Regulatory Certificates EU Medical Device Regulations 3
N Brexit Combination Product Regulatory pathway for UK (MHRA). UK Medical Device Regulations 1
MaHoDie Regulatory compliance for IVD in india Other Medical Device Regulations World-Wide 2
A New to QMS and regulatory... advice on training/certification? ISO 13485:2016 - Medical Device Quality Management Systems 1
A Class 2a CE Mark Regulatory Pathway CE Marking (Conformité Européene) / CB Scheme 1
C Regulatory requirements of cloud platform for devices developed in compliance with 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 5
A CE-Mark regulatory advice - US based Organization CE Marking (Conformité Européene) / CB Scheme 6
J Regulatory path to enter EU market for non medical 60601 component Other Medical Device Regulations World-Wide 2
Justanobody PAD printing and meeting regulatory requirements Manufacturing and Related Processes 10
A Metadata For Drugs, API's, Regulatory & Clinical Documents and Dossier Service Industry Specific Topics 2
S Training for PRRC (person responsible for regulatory compliance) EU Medical Device Regulations 3
V Software license key regulatory requirements Medical Information Technology, Medical Software and Health Informatics 9
H Medical Devices Regulatory Intelligence for International Markets ISO 13485:2016 - Medical Device Quality Management Systems 1
D IS0 13485 - Design perspective to regulatory requirement. ISO 13485:2016 - Medical Device Quality Management Systems 3

Similar threads

Top Bottom