SBS - The best value in QMS software

Certifying a "virtual" company with zero employees

chris1price

Trusted Information Resource
#11
In addition to describing what happens in the Quality Manual, you may also need a Quality/Management/Service Agreement between the companies, essentially saying that Company B is subcontracting the QMS functions to Company A.
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
M ASPICE Certification - Certifying bodies available in India IATF 16949 - Automotive Quality Systems Standard 0
C TL-9000 Certifying Body Issue - Auditor failed to find an issue for 10 years TL 9000 Telecommunications Standard and QuEST 16
S EASA Part 145 - The difference between non-certifying staff and Certifying staff Federal Aviation Administration (FAA) Standards and Requirements 2
O Hardness Testing and Certifying Product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
A Certifying Structural Weldments ROPS Manufacturing and Related Processes 6
D Certifying a New Manufacturing Only Site IATF 16949 - Automotive Quality Systems Standard 1
M Certifying a company with two employees to ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
A Quality Assurance Stamps and Supplies for Certifying Product Misc. Quality Assurance and Business Systems Related Topics 2
P Merging 2 sites into 1 new site and certifying product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
J Certifying Staff Training in a Part 21/145 organisation Training - Internal, External, Online and Distance Learning 3
B Certifying our house for Hardness and Conductivity Testing General Measurement Device and Calibration Topics 8
M Certification Body in South Africa with experience certifying medical labs Registrars and Notified Bodies 5
J Possibility of certifying to IMS (ISO 9001, ISO 14001 & OHSAS 18001) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
N Reputations of ISO 9001 Certifying Bodies (Registrars) - SGS, AJA, BVQI, SAI Global Registrars and Notified Bodies 5
K Certifying Existing Hardness Tester Indenters / Penetrators General Measurement Device and Calibration Topics 9
Q Certifying Gage Blocks on an In-House CMM (Coordinate Measuring Machine) General Measurement Device and Calibration Topics 19
F Certifying for Calibrations of Network Analyzers - Looking for classes/training General Measurement Device and Calibration Topics 1
W Certifying a PDA as a medical device - (FDA/CE) - For use in the operating room ISO 13485:2016 - Medical Device Quality Management Systems 2
K Compelling reasons for a certifying agency to withdraw a ISO certificate? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
B How many approved certifying (registration) bodys are there in the UK? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
B Certifying A Seltered Company QS-9000 - American Automotive Manufacturers Standard 1
M Calibration Procedures for checking and certifying micrometers and calipers General Measurement Device and Calibration Topics 3
T What is the best procedure for calibrating / certifying our Calipers? General Measurement Device and Calibration Topics 8
Marc Certifying Internal Auditors - Unneccessary, Unwanted RAB Intervention ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 4
S Distinction between a critical supplier and a Virtual manufacturer EU Medical Device Regulations 2
L IATF external audit virtual (remote) IATF 16949 - Automotive Quality Systems Standard 13
P Best european location to set up for a virtual medical device manufacturer? EU Medical Device Regulations 4
P New Global HQ Suggestions for Virtual manufacturing/own brand labelling of medical devices? EU Medical Device Regulations 4
P Best Global Option to become an OBL/PLM/Virtual medical device brand in 2020 Other Medical Device Regulations World-Wide 2
GStough WCQI Virtual Conference May 6, 2020 Coffee Break and Water Cooler Discussions 1
D Virtual Documentation via Master Flow Chart? Process Maps, Process Mapping and Turtle Diagrams 4
V CE Mark under MDD or IVDR - IVD company doing Virtual Manufacturing Other Medical Device Regulations World-Wide 3
S ISO 13485 scope of certification - We are a virtual manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 1
M Informational MHRA – Virtual manufacturing of medical devices – Updated guidance Medical Device and FDA Regulations and Standards News 1
dgrainger MHRA guidance on Virtual manufacturing - version 2 EU Medical Device Regulations 1
M Medical Device News CDRH Research Programs – VICTRE: Virtual Imaging Clinical Trials for Regulatory Evaluation Medical Device and FDA Regulations and Standards News 0
J Virtual Manufacturer and CE Marking EU Medical Device Regulations 8
M Virtual Manufacturer vs Reseller (Medical Devices) EU Medical Device Regulations 0
TheMightyWife Virtual Manufacturer v Medical Device File (NB audit) EU Medical Device Regulations 12
N Own brand labelling/virtual manufacture of IVD's EU Medical Device Regulations 2
S Virtual manufacturers/OEM - CE/ISO requirements EU Medical Device Regulations 7
B Virtual Manufacturer / OBL ISO Requirements Other ISO and International Standards and European Regulations 3
M Audit Mandays for OBL/Virtual Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 9
W Virtual Manufacturer and Risk Management ISO 14971 - Medical Device Risk Management 3
I MHRA - Virtual Manufacturer Document Requirements EU Medical Device Regulations 2
K Quality Manual for a Virtual Company (Medical Device) Quality Management System (QMS) Manuals 2
P Qualification of pest control service in a "virtual manufacturer" ISO 13485:2016 - Medical Device Quality Management Systems 3
P How to add Voip features (ring group, virtual receptionist) into Cisco SIP PBX in C#? Medical Information Technology, Medical Software and Health Informatics 1
J FDA Compliant Quality System for Virtual Manufacturing (IVD Medical Device)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
W ISO 13485 - The use of virtual offices (everything is sub-contracted) ISO 13485:2016 - Medical Device Quality Management Systems 4

Similar threads

Top Bottom