Otsingu
tulemused

Credit score:

Reliable

Reputation score:

2,840

Employees:

–

Forecast turnover (2026):

–

Reliable family reconciliation and training union

We support the resolution of disputes between families and parties outside the courtroom. We offer training, accreditation, standards and public information and guidance to mediators.

• certification

• ethical requirements

• family mediation

• intermediary training

• accreditation

• ethics

• public information

• solution to family conflicts

• voluntary mediation

• confidentiality

• continuing training

• professional examination

• professional standards

• qualification requirements

• activities of other professional organisations

Credit score:

Reliable

Reputation score:

1,750

Employees:

–

Forecast turnover (2026):

–

Development and skills based on strengths

We offer training, counselling, psychotherapy, supervision and coaching to individuals, professionals and organizations. We work based on strengths to develop skills and support sustainable change.

• ethical support

• personal support

• supervision

• professional development

• instructions

• psychotherapy

• mental health

• emotional work

• communication

• presentation skills

• teamwork

• continuing training

• training

• coaching

• consultation

• other training courses

Credit score:

Reliable

Reputation score:

550

Employees:

1

Forecast turnover (2026):

85,958 €

All other professional, scientific and technical activities n.e.c.

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

• preservation of relevant documentation of the study

• ethical conduct in clinical trials

• clinical trial monitoring

• study protocols

• patient safety

• cooperation with research centres

• clinical trial monitoring services

• study protocol development

• patient safety in clinical trials

• clinical study documentation preservation

• research centre collaboration

• clinical research monitoring

• clinical trial compliance

• patient recruitment for studies

• clinical trial management

• regulatory documentation clinical trials

• clinical trial quality assurance

• data management in clinical trials

• clinical trial site coordination

• phase i monitoring

• phase ii-iii monitoring

• follow-up monitoring

• compliance with safety

• administration of study protocol

• investigative files

• regulatory presentations

• readiness for audit

• all other professional, scientific and technical activities n.e.c.