Mdr: vind de beste diensten

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

229 beschikbare diensten

mdr medical device regulations

S

Niveau 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

provide eu mdr 2017 technical documentation

Z

I will provide eu mdr 2017 technical documentation

5,0(1)

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 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

medical devices eu mdr ivdr notified body compliance

M

Niveau 2

I will medical devices eu mdr ivdr notified body compliance

5,0(9)

provide eu rep, eudamed eu mdr documentation

H

I will provide eu rep, eudamed eu mdr documentation

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

V

Niveau 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

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

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

develop iso 13485, UK mdr, technical documentation

N

Niveau 2

I will develop iso 13485, UK mdr, technical documentation

5,0(2)

Biedt videoconsultatie aan

help with your eu mdr ce, medical devices strategy

H

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

prepare medical device technical file for mdr registration

L

Niveau 2

I will prepare medical device technical file for mdr registration

5,0(2)

Vanaf US$ 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

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

do mhra registration ukca certificate mdr documentation and fda compliance

Z

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

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

A

Niveau 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

medical devices eu mdr ivdr notified body compliance

K

Kendra Tabhitha

I will medical devices eu mdr ivdr notified body compliance

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

perform eu mdr ce medical device strategy and consulting

M

I will perform eu mdr ce medical device strategy and consulting

5,0(1)

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

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)

create customized surgical instrument technical drawings for mdr

F

Niveau 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

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

B

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

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

T

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

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

A

Niveau 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

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

do tech documentation mdr sfda fda ukca tga and amazon devices

h

Niveau 1

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

5,0(4)

prepare mdr documentation for your medical device ce marking

C

I will prepare mdr documentation for your medical device ce marking

1
2
3
4
5

Mdr: gerelateerde diensten

Technische teksten Medisch hulpmiddel Iso 13485 CE-certificering Ukca EU MDR FDA MHRA FDA compliance Medische apparatuur