Mdr: encuentra los mejores servicios

Mdr: obtén los mejores servicios freelance para completar tus proyectos con éxito.

230 servicios disponibles

mdr medical device regulations

S

Nivel 2

I will mdr medical device regulations

5.0(9)

review medical device mdr technical documentation

P

I will review medical device mdr technical documentation

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

N

I will provide eu rep, eudamed, eu mdr documentation

5.0(4)

make technical drawings for surgical instruments mdr

S

I will make technical drawings for surgical instruments mdr

5.0(3)

write medical ebooks for neuroscience nursing and mdr educators

B

I will write medical ebooks for neuroscience nursing and mdr educators

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)

provide eu mdr 2017 technical documentation

Z

I will provide eu mdr 2017 technical documentation

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

do eu mdr technical file remediation

Z

I will do eu mdr technical file remediation

provide eu rep, eudamed eu mdr documentation

H

I will provide eu rep, eudamed eu mdr documentation

medical devices eu mdr ivdr notified body compliance

M

Nivel 2

I will medical devices eu mdr ivdr notified body compliance

5.0(9)

act as mdr prrc for companies under 50 employees and under 10 million euro

V

Nivel 2

I will act as mdr prrc for companies under 50 employees and under 10 million euro

5.0(34)

optimize mdr fees and ensure payment compliance for your business

E

I will optimize mdr fees and ensure payment compliance for your business

handle mhra registration, ukca certificate, fda and mdr compliance

c

I will handle mhra registration, ukca certificate, fda and mdr compliance

provide iso 13485 consulting, mdr compliance certification preparation

A

I will provide iso 13485 consulting, mdr compliance certification preparation

help with your eu mdr ce, medical devices strategy

H

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

do mhra registration, ukca certificate, fda compliance and mdr documentation

J

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

do mhra registration, ukca certificate, fda compliance and mdr documentation

H

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

prepare medical device technical file for mdr registration

L

Nivel 2

I will prepare medical device technical file for mdr registration

5.0(2)

Desde USD 4,800

design precision engineer medical devices, mdr medical device regulations

N

I will design precision engineer medical devices, mdr medical device regulations

do iso 13485, ce marking, mdr documentation

N

I will do iso 13485, ce marking, mdr documentation

develop iso 13485, UK mdr, technical documentation

N

Nivel 2

I will develop iso 13485, UK mdr, technical documentation

5.0(2)

Ofrece video consultas

do mhra registration, ukca certificate, fda compliance and mdr documentation

A

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

do mhra registration, ukca certificate, fda compliance and mdr documentation

H

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

do mhra registration, ukca certificate, fda compliance and mdr documentation

O

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

do mhra registration, ukca certificate, fda compliance and mdr documentation

M

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

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

C

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

medical devices eu mdr ivdr notified body compliance

K

Kendra Tabhitha

I will medical devices eu mdr ivdr notified body compliance

perform eu mdr ce medical device strategy and consulting

M

I will perform eu mdr ce medical device strategy and consulting

5.0(1)

do mhra registration ukca certificate mdr documentation and fda compliance

Z

I will do mhra registration ukca certificate mdr documentation and fda compliance

create customized surgical instrument technical drawings for mdr

F

Nivel 1

I will create customized surgical instrument technical drawings for mdr

5.0(1)

do iso 13485, ce mark with rep, doc, eudamed and mdr documentation

A

Nivel 1

I will do iso 13485, ce mark with rep, doc, eudamed and mdr documentation

5.0(1)

do mhra registration, ukca certification, medical device compliance and mdr docu

V

I will do mhra registration, ukca certification, medical device compliance and mdr docu

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

assist with eu mdr ce medical devices strategy iso 13485

H

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

prepare mdr technical documentation and ce marking for your medical device

H

I will prepare mdr technical documentation and ce marking for your medical device

do mhra registration, ukca certificate, fda compliance and mdr documentation

A

Nivel 1

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

4.8(4)

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

handle mhra registration, ukca certificate, fda compliance and mdr documentation

A

I will handle mhra registration, ukca certificate, fda compliance and mdr documentation

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

handle mhra registration, ukca certificate, fda compliance and mdr documentation

T

I will handle mhra registration, ukca certificate, fda compliance and mdr documentation

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

P

Nivel 2

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

4.7(4)

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

prepare mdr documentation for your medical device ce marking

C

I will prepare mdr documentation for your medical device ce marking

do tech documentation mdr sfda fda ukca tga and amazon devices

h

Nivel 1

I will do tech documentation mdr sfda fda ukca tga and amazon devices

5.0(4)

do mhra registration, ukca certificate, fda compliance and mdr documentation

B

I will do mhra registration, ukca certificate, fda compliance and mdr documentation

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Mdr: servicios relacionados

Escritura técnica Dispositivo médico Iso 13485 Ukca Marcado ce MDR de la UE Fda MHRA Cumplimiento de fda Dispositivos médicos