University Medical Research

UniMR

NDK

Sofia, Bulgaria. This is an old site of UniMR is a Bulgarian contract research and development organization dedicated to helping pharmaceutical and biotechnology companies efficiently in order to bring new drugs, biologics, and medical devices to the people who need them.

Useful links: fertilaid


Services


Medical Services in Bulgaria offered from Univercity Medical Research in Bulgaria are Regulatory Affairs, Feasibility, Clinical monitoring, Project Managment, Drug hadling. 

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Advantages


Advantages for conducting clinical trials in Bulgaria managed by UniMR

Rapid start-up

  • The regulatory approval process is well defined. The average approval time in Bulgaria is between 75 and 90 days. Our project teams are concentrated in rapid initiation of all centres after approval by the Competent Authority. We aim at an average time of 20-30 days between the approval date and the first subject included in the country.

Fast patient recruitment

  • Large patient populations are available in most therapeutic fields. Bulgarian Investigators are motivated to prove that they can successfully fulfil their commitments within the agreed timelines and at the highest quality standards.

Excellent quality

  • The excellence in quality is proven by the positive results from international independent audits and local regulatory inspections.

Qualified monitoring resources

  • All our monitors are physicians trained in ICH-GCP. This enables perfect communication with the Investigators and high quality standards in the monitoring process.

Financial advantage

  • Compared with Western and Central Europe we can offer lower costs for investigators fees and CRO services without compromising quality.

>>

Contacts


UniMR Bul. "D-r Petar Dertliev" 81, 1336 Sofia, Bulgaria

Tel: +359 879 55 32 58, Fax:  + 359 2 892 74 15

>>

Services


Medical Services in Bulgaria offered from Univercity Medical Research in Bulgaria are Regulatory Affairs, Feasibility, Clinical monitoring, Project Managment, Drug hadling. 

>>

Advantages


Advantages for conducting clinical trials in Bulgaria managed by UniMR

Rapid start-up

  • The regulatory approval process is well defined. The average approval time in Bulgaria is between 75 and 90 days. Our project teams are concentrated in rapid initiation of all centres after approval by the Competent Authority. We aim at an average time of 20-30 days between the approval date and the first subject included in the country.

Fast patient recruitment

  • Large patient populations are available in most therapeutic fields. Bulgarian Investigators are motivated to prove that they can successfully fulfil their commitments within the agreed timelines and at the highest quality standards.

Excellent quality

  • The excellence in quality is proven by the positive results from international independent audits and local regulatory inspections.

Qualified monitoring resources

  • All our monitors are physicians trained in ICH-GCP. This enables perfect communication with the Investigators and high quality standards in the monitoring process.

Financial advantage

  • Compared with Western and Central Europe we can offer lower costs for investigators fees and CRO services without compromising quality.

>>

Contacts


UniMR Bul. "D-r Petar Dertliev" 81, 1336 Sofia, Bulgaria

Tel: +359 879 55 32 58, Fax:  + 359 2 892 74 15

>>
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