Mdr: encuentra los mejores servicios

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

228 servicios disponibles

mdr medical device regulations

S

I will mdr medical device regulations

5.0(9)

prepare ce mdr technical documentation and technical file

M

I will prepare ce mdr technical documentation and technical file

5.0(1)

provide eu rep, eudamed, eu mdr documentation

N

I will provide eu rep, eudamed, eu mdr documentation

5.0(4)

provide eu rep, eudamed, eu mdr documentation

A

I will provide eu rep, eudamed, eu mdr documentation

5.0(1)

perform eudamed registration for eu mdr devices

M

Nivel 1

I will perform eudamed registration for eu mdr devices

write medical ebooks for neuroscience nursing and mdr educators

B

I will write medical ebooks for neuroscience nursing and mdr educators

design compliant eu mdr powerpoint for training or audit

A

I will design compliant eu mdr powerpoint for training or audit

5.0(1)

develop iso 13485 documentation and eu mdr

o

I will develop iso 13485 documentation and eu mdr

provide eu mdr 2017 technical documentation

Z

I will provide eu mdr 2017 technical documentation

5.0(1)

provide eu rep, eudamed eu mdr documentation

H

I will provide eu rep, eudamed eu mdr documentation

do eu mdr technical file remediation

Z

I will do eu mdr technical file remediation

help with your eu mdr ce, medical devices strategy

H

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

write construction method statements, mdr and project reports

F

I will write construction method statements, mdr and project reports

medical devices eu mdr ivdr notified body compliance

M

Nivel 2

I will medical devices eu mdr ivdr notified body compliance

5.0(9)

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

do iso 13485, ce marking, mdr documentation

N

I will do iso 13485, ce marking, mdr documentation

act as your external prrc according to eu mdr

L

I will act as your external prrc according to eu mdr

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(35)

optimize mdr fees and ensure payment compliance for your business

E

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

perform eu mdr ce medical device strategy and consulting

M

Nivel 1

I will perform eu mdr ce medical device strategy and consulting

5.0(1)

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

T

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 registration eu mdr documentation

C

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

create customized surgical instrument technical drawings for mdr

F

Nivel 1

I will create customized surgical instrument technical drawings for mdr

5.0(1)

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 compliance and mdr documentation

A

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

do UK mhra registration, ukca marking, and mdr compliance

S

I will do UK mhra registration, ukca marking, and mdr compliance

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 registration, ukca certificate, fda compliance and mdr documentation

A

I will handle 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

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

prepare mdr compliance, cgmp documentation, mocra compliance and fda regulatory

W

I will prepare mdr compliance, cgmp documentation, mocra compliance and fda regulatory

prepare mdr documentation for your medical device ce marking

C

I will prepare mdr documentation for your medical device ce marking

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

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)

prepare iso 13485 documents, eu mdr and medical device technical documentation

P

I will prepare iso 13485 documents, eu mdr and medical device technical documentation

prepare mdr technical documentation and ce marking for your medical device

J

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

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

handle medical device products certification for ce, fda, ukca, and mdr

L

I will handle medical device products certification for ce, fda, ukca, and mdr

develop complete eu UK mdr technical file regulatory support

N

Nivel 2

I will develop complete eu UK mdr technical file regulatory support

5.0(2)

Ofrece video consultas

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)

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

B

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

mdr iso 13485 iec 60601 medical device compliance and documentation

K

Kendra Tabhitha

I will mdr iso 13485 iec 60601 medical device compliance and documentation

handle mhra registration, ukca, eu mdr and fda medical device compliance

H

I will handle mhra registration, ukca, eu mdr and fda medical device compliance

do mdr iso 13485 iec 60601 medical device compliance and documentation

H

Nivel 1

I will do mdr iso 13485 iec 60601 medical device compliance and documentation

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)

provide fda medical device compliance, ce marking, eu mdr and ukca

S

I will provide fda medical device compliance, ce marking, eu mdr and ukca

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Mdr: servicios relacionados

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