We optimize your clinical research, whether you need help designing an entire clinical study or standalone services, we provide custom and flexible solutions that meet your unique needs.
Medicorent Int. AB is a Scandinavian company providing CRO services within a wide range of therapeutic areas. Our strength comes from adjusting tactics quickly to meet Customer demands and a strong network and ability to put talented teams together to handle projects in a highly effective way. We bring the expertise to strengthen your operational management.

 

END-2-END CLINICAL DEVELOPMENT SERVICES 

Our specialized medical and clinical research & data management team provides medical expertise and a complete strategic Development, Management and Analysis of programs that support the Clinical Development. Our operational expertise within clinical development support in the conduct of clinical trials in Phase I-IV studies on both local and European basis.

With our operational flexibility we have the ability to provide full-service solutions or a stand-alone solutions, whatever benefits your company.

Services include:

·    Medical Writing

·    Biostatistics

·    Clinical Operations

·    RWE/Register studies

·    HECON

·    Clinical Data Management/eDC     

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STRATEGIC ADVISORY PARTNER

Our experienced Regulatory Team provide services throughout the entire registration process. From the pre-clinical phase through the complete development of the product to the market and maintenance, we offer support with Regulatory approvals and registrations. We establish planning strategies both for non-clinical and clinical programs and along with medical statistics.

 

Our experienced team has both national, EU and international knowledge in regulatory requirements and can support you in:

• Full Regulatory Review and Support

• Advisory Board Support and Review

• Scientific Advice Preparation

• Regulatory Support for Clinical Trial Applications

• Full MAA Management and Preparation

• CMC, Non- Clinical & Clinical Data Review and Gap Analysis

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CRO & SUPPORTIVE SERVICES TO MEET CLIENTS NEEDS:

• Clinical Development Technology:
  eCRF/EDC, ePRO, eTMF, TrialHub site portal, IT Infrastructure

• System Validation

• Quality Management

• Medical Information

• Pharmacovigilance