EU MDR: vind de beste diensten

EU MDR: ontdek hier de beste freelance diensten voor een succesvolle afronding van je project.

147 beschikbare diensten

provide eu mdr 2017 technical documentation

Z

I will provide eu mdr 2017 technical documentation

5,0(1)

do eu mdr technical file remediation

Z

I will do eu mdr technical file remediation

provide eu rep, eudamed, eu mdr documentation

A

I will provide eu rep, eudamed, eu mdr documentation

5,0(1)

provide eu rep, eudamed eu mdr documentation

H

I will provide eu rep, eudamed eu mdr documentation

provide eu rep, eudamed, eu mdr documentation

N

I will provide eu rep, eudamed, eu mdr documentation

5,0(4)

perform eudamed registration for eu mdr devices

M

I will perform eudamed registration for eu mdr devices

design compliant eu mdr powerpoint for training or audit

A

I will design compliant eu mdr powerpoint for training or audit

5,0(1)

medical devices eu mdr ivdr notified body compliance

M

Niveau 2

I will medical devices eu mdr ivdr notified body compliance

5,0(9)

be your eu mdr consultant and write your clinical evaluation cer

D

I will be your eu mdr consultant and write your clinical evaluation cer

perform eu mdr ce medical device strategy and consulting

M

I will perform eu mdr ce medical device strategy and consulting

5,0(1)

provide eu mdr medical device compliance consulting and documentation support

A

I will provide eu mdr medical device compliance consulting and documentation support

help with your eu mdr ce, medical devices strategy

H

I will help with your eu mdr ce, medical devices strategy

prepare clinical technical files for sfda fda 510k and eu mdr

H

I will prepare clinical technical files for sfda fda 510k and eu mdr

medical devices eu mdr ivdr notified body compliance

K

Kendra Tabhitha

I will medical devices eu mdr ivdr notified body compliance

provide eu mdr and ivdr regulatory consulting for medical devices

B

I will provide eu mdr and ivdr regulatory consulting for medical devices

provide eu mdr ce and iso 13485 mediacal device certification

C

I will provide eu mdr ce and iso 13485 mediacal device certification

provide iso 13485 documentation and eu mdr medical device compliance

C

I will provide iso 13485 documentation and eu mdr medical device compliance

be your eu responsible person for gpsr, msr, fbo, mdr

M

I will be your eu responsible person for gpsr, msr, fbo, mdr

4,9(5)

prepare eu mdr technical documentation, ce marking compliance for medical device

J

I will prepare eu mdr technical documentation, ce marking compliance for medical device

assist with eu mdr ce medical devices strategy iso 13485

H

I will assist with eu mdr ce medical devices strategy iso 13485

do mhra registration, ukca certificate, fda registration eu mdr documentation

C

I will do mhra registration, ukca certificate, fda registration eu mdr documentation

provide eu mdr and ce medical device strategy with iso 13485

J

I will provide eu mdr and ce medical device strategy with iso 13485

english to german medical translation eu mdr compliance and clinical reports

L

I will english to german medical translation eu mdr compliance and clinical reports

handle mhra, ukca, fda and eu mdr compliance for medical devices

R

I will handle mhra, ukca, fda and eu mdr compliance for medical devices

act as mdr prrc eu mdr compliant technical documentation technical file ce 13485

L

I will act as mdr prrc eu mdr compliant technical documentation technical file ce 13485

do fda 510k eu mdr ivdr mhra sfda medical device compliance

J

I will do fda 510k eu mdr ivdr mhra sfda medical device compliance

be your medical device regulatory consultant for eu mdr, fda 510k, and iso 13485

B

I will be your medical device regulatory consultant for eu mdr, fda 510k, and iso 13485

provide fda eu mdr ivdr mhra medical device compliance support

N

I will provide fda eu mdr ivdr mhra medical device compliance support

create eu mdr technical file, ce marking documentation, conformity dossier prep

E

I will create eu mdr technical file, ce marking documentation, conformity dossier prep

help with fda 510k ce marking eu mdr ivdr medical device compliance

J

I will help with fda 510k ce marking eu mdr ivdr medical device compliance

provide iso 13485, eu rep, srn, eudamed and mdr technical documentation

P

Niveau 2

I will provide iso 13485, eu rep, srn, eudamed and mdr technical documentation

4,7(4)

handle eu mdr ivdr compliance, eudamed, ce fda ukca certification and eu rep

M

I will handle eu mdr ivdr compliance, eudamed, ce fda ukca certification and eu rep

help you with eu mdr ce medical device strategy iso 13485

H

I will help you with eu mdr ce medical device strategy iso 13485

do mdr medical device peptide website eu mdr peptide store ce marking iso 13485

T

I will do mdr medical device peptide website eu mdr peptide store ce marking iso 13485

handle eu mdr, ce marking, iso 13485, iso 27001 and fda registration for medical

N

I will handle eu mdr, ce marking, iso 13485, iso 27001 and fda registration for medical

be your eu responsible person for gpsr, mdr, ce mark, authorized representative

N

I will be your eu responsible person for gpsr, mdr, ce mark, authorized representative

handle eu mdr ce iso 13485, 27001 fda registration and medical device compliance

D

I will handle eu mdr ce iso 13485, 27001 fda registration and medical device compliance

perform an eu ai act and mdr compliance technical review and gap analysis

L

I will perform an eu ai act and mdr compliance technical review and gap analysis

handle eu mdr ce iso 13485 27001 fda registration and medical device

A

I will handle eu mdr ce iso 13485 27001 fda registration and medical device

help you achieve iso 13485, eu mdr, and ce marking for your medical device

S

Niveau 1

I will help you achieve iso 13485, eu mdr, and ce marking for your medical device

manage eu mdr , iso 13485 qms, ce, fda, srn, ukca, eu rep and eudamed

B

I will manage eu mdr , iso 13485 qms, ce, fda, srn, ukca, eu rep and eudamed

your eu responsible person gpsr, gdpr, espr, msr, fbo, mdr

N

I will your eu responsible person gpsr, gdpr, espr, msr, fbo, mdr

handle eu mdr ce iso 13485, 27001 fda registration amd medical device compliance

M

I will handle eu mdr ce iso 13485, 27001 fda registration amd medical device compliance

provide medical device regulatory affairs support for US fda eu mdr iso 13485

A

I will provide medical device regulatory affairs support for US fda eu mdr iso 13485

handel eu mdr ce iso 13485, 27001 fda registration and medical device compliance

N

I will handel eu mdr ce iso 13485, 27001 fda registration and medical device compliance

fda registration fda facility medical ndc eu mdr ce device listing 510k dossier

A

I will fda registration fda facility medical ndc eu mdr ce device listing 510k dossier

do eu mdr medical device ce marking, iso 27001, fda compliance, ukca and mhra

o

I will do eu mdr medical device ce marking, iso 27001, fda compliance, ukca and mhra

deliver iso 13485 qms, ce mark, eu rep, eudamed srn, mdr technical documents

A

I will deliver iso 13485 qms, ce mark, eu rep, eudamed srn, mdr technical documents

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EU MDR: gerelateerde diensten

Medisch hulpmiddel Mdr CE-certificering Iso 13485 Ukca FDA MHRA FDA compliance MHRA-registratie Regelgevende zaken