Otsingu
tulemused

Credit score:

Reliable

Reputation score:

1,990

Employees:

–

Forecast turnover (2024):

–

Carriage of passengers in Tartu

transport of the sick and people with special needs, wheelchair transport, transport of the sick 24h, transport of people with special needs, non-exceptional patient transport, Medical Transport, transport solutions for people with disabilities, 24 hour medical taxi, transport with lying bed, transport options for people with reduced mobility

• transport of the sick 24h

• non-exceptional patient transport

• non-emergency patient transport

• 24/7 emergency patient transport

• measures for patient safety and comfort

• transport of the sick and people with special needs

• wheelchair transport

• transport of people with special needs

• medical transport

• transport solutions for people with disabilities

• 24 hour medical taxi

• transport with lying bed

• transport options for people with reduced mobility

• non-exceptional medical transport

• transport of the elderly

• carriage of passengers

• transport of the sick and people with special needs

• special needs transportation

• passenger carriage service

• disability transport solutions

• non-emergency medical transportation

• wheelchair transport services

• 24/7 sick transport

• medical transport services

• 24 hour medical taxi service

• lying bed transport

• reduced mobility transport options

• elderly transportation service

• tartu medical transport

• wheelchair accessible vehicles

Credit score:

Reliable

Reputation score:

940

Employees:

1

Forecast turnover (2024):

156,375 €

Other activities in Tartu

phase ii-iii monitoring, regulatory documentation clinical trials, clinical trial quality assurance, data management in clinical trials, clinical trial site coordination, ethical conduct in clinical trials, phase i monitoring, regulatory presentations, investigative files, administration of study protocol

• patient safety

• patient safety in clinical trials

• patient recruitment for studies

• compliance with safety

• clinical trial monitoring

• study protocols

• preservation of relevant documentation of the study

• cooperation with research centres

• clinical trial monitoring services

• study protocol development

• clinical study documentation preservation

• research centre collaboration

• clinical research monitoring

• clinical trial compliance

• clinical trial management

• regulatory documentation clinical trials

• clinical trial quality assurance

• data management in clinical trials

• clinical trial site coordination

• ethical conduct in clinical trials

• phase i monitoring

• phase ii-iii monitoring

• follow-up monitoring

• administration of study protocol

• investigative files

• regulatory presentations

• readiness for audit

• other activities