Otsingu
tulemused

Credit score:

Reliable

Reputation score:

2,530

Workers:

1

Estimated turnover (2024):

113,476 €

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• study protocols

• preservation of relevant documentation of the study

• study protocol development

• clinical study documentation preservation

• regulatory documentation clinical trials

• clinical trial monitoring

• patient safety

• cooperation with research centres

• clinical trial monitoring services

• patient safety in clinical trials

• research centre collaboration

• clinical research monitoring

• clinical trial compliance

• patient recruitment for studies

• clinical trial management

• 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

• compliance with safety

• administration of study protocol

• investigative files

• regulatory presentations

• readiness for audit

• other activities