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Welcome to Central & Eastern European Research Institute!

Site Management and Monitoring. Central and Eastern European Research Institute (CEERI) is a clincal research institution that supports studies across several countries in Central and Eastern Europe. CEERI has supported several pharmaceutical companies in developing clinical research studies across its medical sites. CEERI has also a large team of Principal Investigators with previous experience in clinical trials in almost all the therapeutic areas. We look forward to working with you!

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Welcome to Central & Eastern European Research Institute! | cee-ri.com Reviews
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Site Management and Monitoring. Central and Eastern European Research Institute (CEERI) is a clincal research institution that supports studies across several countries in Central and Eastern Europe. CEERI has supported several pharmaceutical companies in developing clinical research studies across its medical sites. CEERI has also a large team of Principal Investigators with previous experience in clinical trials in almost all the therapeutic areas. We look forward to working with you!
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2 our services
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4 investigators and researchers
5 career
6 leadership
7 locations
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Welcome to Central & Eastern European Research Institute! | cee-ri.com Reviews

https://cee-ri.com

Site Management and Monitoring. Central and Eastern European Research Institute (CEERI) is a clincal research institution that supports studies across several countries in Central and Eastern Europe. CEERI has supported several pharmaceutical companies in developing clinical research studies across its medical sites. CEERI has also a large team of Principal Investigators with previous experience in clinical trials in almost all the therapeutic areas. We look forward to working with you!

INTERNAL PAGES

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Welcome to Central & Eastern European Research Institute's Website! - Services >> Feasibility Studies

http://www.cee-ri.com/pages/Feasibilitystudies.html

Site Management and Monitoring. With vast experience of hundreds of clinical studies, CEERI multi disciplinary staff will bring to our sponsors excellent insight to their studies. Launching a Feasibility study is a excellent step for the success of a large study. We encourage our sponsors to contact us to assist them in developing feasibility studies including all aspects of patient recruitment, inclusion and exclusion criteria, protocol writing and regulatory compliance.

2

Welcome to Central & Eastern European Research Institute's Website! - Investigators & Researchers >> FAQ

http://www.cee-ri.com/pages/FAQ-PI.html

Site Management and Monitoring. Investigators and Researchers FAQ. 1 What is a review preparatory to research? 2 As a Clinical Investigator, do you need to be compliant with HIPAA? 3 What is Quality Assurance in research? There is a system of checks and balances in place for the conduct of clinical research. Regulations and guidelines make up part of this system. Quality assurance (QA) professionals use these tools as they conduct audits to assess compliance with Good Clinical Practice (GCP). Conducting ...

3

Welcome to Central & Eastern European Research Institute's Website! - Investigators & Researchers >> PI Enrollment

http://www.cee-ri.com/pages/PIEnrollment.html

Site Management and Monitoring. Investigators and Researchers PI Enrollment. If you are interested in participating in a clinical trial as a Principal Investigator, please complete the form below or simply submit your CV at the e-mail below. All information will be kept confidential, in alignment with health privacy laws and regulations. Following submission of this information, you will receive a follow-up response from our staff. Note: All required fields are marked with an asterisk ( *.

4

Welcome to Detroit Clinical Research Center's Website! - Services >> Biostatistics

http://www.cee-ri.com/pages/Biostatistics.html

Site Management and Monitoring. CEERI members in the statistical department have important contributions to the development of statistical methodology and they provide the quantitative component to health and biomedical research efforts that have had a major impact on the prevention and treatment of disease. Our research efforts are internationally recognized in area of health services and clinical research.

5

Welcome to Central & Eastern European Reasearch Institute's Website! - Services >> Data Management

http://www.cee-ri.com/pages/DataManagement.html

Site Management and Monitoring. At CEERI, we realize the importance of Data Management in the success, accuracy and safety of data. We therefore employ advanced tools lead by staff with extensive experience in data management. Our Data Management services include. Web interface and Graphical User Interface (GUI) for each study and per sponsors requirement. Case report form design: electronic and paper versions. Data entry and status reporting. Standardized Data Collection Processes.

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MPR - Resourcing

http://www.maximax.com/Pages/Resourcing.html

How to contact us. How we can help you! Where we can help you! For some clinical trials projects, all what you need is additional staff support to compliment your teams: MPR will be there for you! We have access to a large pool of candidates with diverse functional and therapeutic backgrounds. We follow flexible and diverse resourcing models. We also partner with several resourcing organization all over the globe to expand our capacities if needed.

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MPR - Bio-Statistics

http://www.mpr-cro.com/Pages/Bio-Statistics.html

How to contact us. How we can help you! Where we can help you! We offer Sponsors comprehensive or partial support for their Bio-Statistical needs. Several of MPR staff and affiliated researchers have extensive experience in Bio Statistical study design, analysis and reporting. In our statistical reporting we adhere to FDA special therapeutic guidelines for statistical reporting.

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MPR and Yamamoto launch international research project

http://www.mpr-cro.com/Pages/Yamamoto_event.html

How to contact us. How we can help you! Where we can help you! MPR and Yamamoto launch an international research project on expanding the application of Hyperthermia in the treatment of several indications of cancer. 11-30-2009: Osaka, Japan. MPR Inc. and Yamamoto Co. launch a joint research and development project to expand the application and use of Hyperthermia in the treatment of several indications of cancer using an innovative medical device, Thermotron-RF8.

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MPR - Regulatory

http://www.mpr-cro.com/Pages/Regulatory.html

How to contact us. How we can help you! Where we can help you! Our regulatory teams can handle the complete trial registration and approval process. MPR`s Regulatory Affairs professionals are dedicated to ensuring the successful and timely submission of IND or NDA applications. A partial list of the regulatory services that we provide includes:. Legal support for the development and registration of the clinical trial based on regulatory requirements. Providing efficient review and approval services.

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MPR - Resourcing

http://www.mpr-cro.com/Pages/Resourcing.html

How to contact us. How we can help you! Where we can help you! For some clinical trials projects, all what you need is additional staff support to compliment your teams: MPR will be there for you! We have access to a large pool of candidates with diverse functional and therapeutic backgrounds. We follow flexible and diverse resourcing models. We also partner with several resourcing organization all over the globe to expand our capacities if needed.

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MPR - Sites & Investigators

http://www.mpr-cro.com/Pages/Sites-and-investigators.html

How to contact us. How we can help you! Where we can help you! If you are interested in participating in a clinical trial as a Site or as a Principal Investigator, please send an e-mail to pi@maximax.com and someone from the Site and PI selection and management department will contact you for more detailed information. You may also complete the form below. All information will be kept confidential, in alignment with health privacy laws and regulations. How we can help you! Where we can help you!

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MPR administers Peramivir

http://www.mpr-cro.com/Pages/Peramivir_event.html

How to contact us. How we can help you! Where we can help you! MPR to administer the emergency use of Peramivir under special regulatory approvals in selected countries. MPR Inc. announced to several MOH in MENA and Gulf region the availability of Peramivir to treat H1N1 flu vaccine under emergency use and special process approval. MPR in collaboration with BioCryst Pharmaceutical Inc. and several regulatory agencies are making the drug available for the treatment of H1N1 during the flu season.

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MPR - Our Services

http://www.mpr-cro.com/Pages/Our-Services.html

How to contact us. How we can help you! Where we can help you! At MPR, we believe that partnership with Sponsors is essential to succeed in conducting clinical trials. Successful clinical trials’ management requires innovative solutions with flexibility and ability to change and adapt. We embrace ANY model that adds value to your project. Full Service CRO Model:.

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MPR - Early Phases

http://www.mpr-cro.com/Pages/Early-Phases.html

How to contact us. How we can help you! Where we can help you! We support early phase projects via several units, geographically located to offer our customers accessibility to a large pool of volunteers with particular demographical characteristics. We follow centralized procedures and SOPs. Research Units Michigan, USA. 2 units used as per needed almost 70 beds each. Highly experienced staff with demonstrated research experience. Emergency units close-by or in same facility building.

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MPR - Commercialization

http://www.mpr-cro.com/Pages/Commercialization.html

How to contact us. How we can help you! Where we can help you! Our Commercialization business is led by Maximax International Inc. and involves several business models:. Integrated Service Provider for Commercialization:. Functional Service Provider for Commercialization:. This line of services involves the different aspects associated with commercialization, including:. Market research and feasibility studies. Regulatory submission and approval. Distributors’ selection and management.

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Welcome to Central & Eastern European Research Institute!

Site Management and Monitoring. Central and Eastern European Research Institute (CEERI) is a clincal research institution that supports studies across several countries in Central and Eastern Europe. CEERI has supported several pharmaceutical companies in developing clinical research studies across its medical sites. CEERI has also a large team of Principal Investigators with previous experience in clinical trials in almost all the therapeutic areas. We look forward to working with you!

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