- Credit score:
- Reliable
- Reputation score:
- 2,580
- Employees:
- –
- Forecast turnover (2024):
- 155,803 €
pre-design, risk management, construction technology, procurement of raw materials, workshop planning, procurement of materials, use of tools, final phase and delivery to the customer, conducting the construction process, delivery building materials
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construction
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monitoring the project
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construction phase and execution
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quality control and monitoring
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final phase and delivery to the customer
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delivery building materials
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project planning
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resource planning
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project management
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construction of buildings
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construction of water and sewerage systems
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interior finishing
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estate management
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design of structures
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calculation of construction costs
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construction plans
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construction process
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risk management
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construction technology
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procurement of raw materials
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workshop planning
-
procurement of materials
-
use of tools
-
pre-design
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conducting the construction process
- 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
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clinical trial monitoring
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clinical research monitoring
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phase i monitoring
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phase ii-iii monitoring
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follow-up monitoring
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study protocols
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patient safety
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preservation of relevant documentation of the study
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cooperation with research centres
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clinical trial monitoring services
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study protocol development
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patient safety in clinical trials
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clinical study documentation preservation
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research centre collaboration
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clinical trial compliance
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patient recruitment for studies
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clinical trial management
-
regulatory documentation clinical trials
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clinical trial quality assurance
-
data management in clinical trials
-
clinical trial site coordination
-
ethical conduct in clinical trials
-
compliance with safety
-
administration of study protocol
-
investigative files
-
regulatory presentations
-
readiness for audit
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other activities