Authorised by competent authority and certified according to DIN ISO 9001
Welcome to
Nova-Clin Medical Research Center
We are your competent, experienced and reliable clinical research service provider accompanying various clinical phases of medicinal product and medical device authorisation, such as:
- Organisation and management of clinical trials as CRO
- Conduct of clinical trials (Phase I-III studies) as CRU
- Medical Writing
- Clinical Trial Application
- Data Management
- Pharmacovigilance
- Monitoring
- Medical Monitoring
In cooperation with our partner company ACC we complete and fulfil your needs, such as:
- Organisation and management of clinical trials
- Responsible for clinical trials as CRO
- Medical writing
- Bioanalytics
- Biometrics
- Scientific consulting
- EU Legal Representative
In cooperation with our partner company DELPH-i we complete and fulfil your needs, such as:
- Quality control testing
- Batch certification
- QP service
- Clinical trial supply
- IMP: Import and EU release
- IMP: Manufacturing (nasal application)
- IMP: Packaging and labelling
- Product development
Factsheet / You can download a summary of our companies here.
Nova-Clin Medical Research Center S.R.L.
Rigoletto 14, 300696 Timisoara, Romania
+40 726 160181 I office@nova-clin.com
Competent Authority approved and certified according DIN ISO 9001
In cooperation with our partner companies ACC and DELPH-i as well as our network, we complete and fulfil your needs for successful product development, marketing authorisation and batch certification. Visit our partner websites:
