Envío a la FDA: encuentra los mejores servicios

Envío a la FDA: obtén los mejores servicios freelance para completar tus proyectos con éxito.

512 servicios disponibles

do fda preparation reviewing and submissions

M

Nivel 2

I will do fda preparation reviewing and submissions

5.0(11)

assist with fda 510k submission, fda registration and device listing

M

I will assist with fda 510k submission, fda registration and device listing

prepare fda 510k submission and regulatory documents

E

I will prepare fda 510k submission and regulatory documents

prepare fda 510k submission and cgmp compliance

B

I will prepare fda 510k submission and cgmp compliance

do fda medical device compliance and 510k submission

G

I will do fda medical device compliance and 510k submission

handle fda registration, 510k submission and cgmp compliance

M

I will handle fda registration, 510k submission and cgmp compliance

provide expert fda regulatory compliance and submission consulting

S

I will provide expert fda regulatory compliance and submission consulting

prepare fda submission dossiers including 510k, gras, and mocra

W

I will prepare fda submission dossiers including 510k, gras, and mocra

do fda 510k submission fda compliance medical device fda registration

L

I will do fda 510k submission fda compliance medical device fda registration

provide fda registration, fda compliance, fsvp, and 510k submission support

J

I will provide fda registration, fda compliance, fsvp, and 510k submission support

handle fda 510k submission clearance, fda label review and compliance

S

I will handle fda 510k submission clearance, fda label review and compliance

prepare your fda 510k submission and support clearance

W

I will prepare your fda 510k submission and support clearance

provide fda registration, fda compliance, 510k submission and fsvp services

P

I will provide fda registration, fda compliance, 510k submission and fsvp services

do fda 510k submission documentation for medical device

I

I will do fda 510k submission documentation for medical device

5.0(1)

do fda 510k submission, device listing, ndc, and fda registration

E

I will do fda 510k submission, device listing, ndc, and fda registration

fda 510k submission, device listing, ndc, fda registration and compliance

C

I will fda 510k submission, device listing, ndc, fda registration and compliance

handle fda 510k submission, fda registration, compliance and regulatory filing

V

I will handle fda 510k submission, fda registration, compliance and regulatory filing

fda medical device registration device listing fda 510k submission documentatio

C

I will fda medical device registration device listing fda 510k submission documentatio

do fda registration, fda 510k submission, ndc registration, device listing

L

I will do fda registration, fda 510k submission, ndc registration, device listing

prepare your fda 510k submission and regulatory pathway strategy

S

I will prepare your fda 510k submission and regulatory pathway strategy

fda registration fda label review fda 510k submission fda compliance be us agent

K

I will fda registration fda label review fda 510k submission fda compliance be us agent

handle fda 510k submission, device listing, ndc, fda registration and compliance

b

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

do fda registration, fda 510k submission, fda compliance, device listing, ndc,

F

I will do fda registration, fda 510k submission, fda compliance, device listing, ndc,

handle fda registration, 510k submission, food labeling and compliance

M

I will handle fda registration, 510k submission, food labeling and compliance

prepare regulatory documents for cdsco, US fda, and ema submissions

A

I will prepare regulatory documents for cdsco, US fda, and ema submissions

prepare fda medical device premarket submissions and 510k documentation

C

I will prepare fda medical device premarket submissions and 510k documentation

handle fda submission, compliance consulting, real estate contracts and claims

D

I will handle fda submission, compliance consulting, real estate contracts and claims

handle fda 510k submission, device listing, ndc, fda registration and compliance

A

Nivel 1

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

5.0(7)

prepare fda 510 submission, medical device registration, and device listing

A

I will prepare fda 510 submission, medical device registration, and device listing

do fda 510k submission, issuance of import permit, fda registration in USA

L

I will do fda 510k submission, issuance of import permit, fda registration in USA

do fda registration label review fda 510k submission fda compliance guidance

J

I will do fda registration label review fda 510k submission fda compliance guidance

handle fda 510k submission, device listing, ndc, fda registration and compliance

P

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

handle fda 510k submission, device listing, ndc, fda registration and compliance

A

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

handle fda 510k submission, device listing, ndc, fda registration and compliance

E

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

fda registration, food, cosmetic, import permit, fda compliance, 510k submission

M

I will fda registration, food, cosmetic, import permit, fda compliance, 510k submission

fda registration, food, cosmetic, import permit, fda compliance, 510k submission

A

I will fda registration, food, cosmetic, import permit, fda compliance, 510k submission

handle fda 510k submission, device listing, ndc, fda registration compliance

B

I will handle fda 510k submission, device listing, ndc, fda registration compliance

handle fda 510k submission, device listing, ndc, fda registration and compliance

E

I will handle fda 510k submission, device listing, ndc, fda registration and compliance

handle fda 510k submission, fda label review and medical device compliance

E

I will handle fda 510k submission, fda label review and medical device compliance

fda 510k submission documentation and US agent service for medical device

K

Kendra Tabhitha

I will fda 510k submission documentation and US agent service for medical device

handle fda 510k submission, device listing, ndc, fda registration and complianc

T

Terrence Mathew

I will handle fda 510k submission, device listing, ndc, fda registration and complianc

do fda 510k submission, device listing ndc fda registration and compliance

s

I will do fda 510k submission, device listing ndc fda registration and compliance

do fda registration, mocra compliance, US agent and fda 510k submission

H

I will do fda registration, mocra compliance, US agent and fda 510k submission

handle fda 510k submission device listing, ndc, fda registration and comp

m

I will handle fda 510k submission device listing, ndc, fda registration and comp

medical device technical drawing, fda submission engineering drawing, medical ca

J

I will medical device technical drawing, fda submission engineering drawing, medical ca

handle fda 510k submission, device listing, ndc, fda registration compliance

A

I will handle fda 510k submission, device listing, ndc, fda registration compliance

handle 510k documentation fda amazon and premarket submissions medical device

E

I will handle 510k documentation fda amazon and premarket submissions medical device

do fda 510k submission,device listing and US agent fda amazon premarket submiss

E

Elizabeth mercy

I will do fda 510k submission,device listing and US agent fda amazon premarket submiss

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