At CroxxMed, we are a team of experienced personnel striving to make your experience as
smooth as possible. Nordic by nature, we provide complex knowledge built on a solid
foundation of years in clinical research within many different therapeutic areas.
CroxxMed offers services in all phases (I-IV); clinical operation, regulatory affairs,
data management, statistics, medical writing, pharmacovigilance, and consulting services
for all types of medical device studies. We are at all times updated on the market. At
any time, fully in tune with the regulatory requirements and trends in the industry. We
are less boring than average, and you are our top priority.
We have a flat infrastructure, short communication routes, efficient dialog, and only experienced employees.
Research Professionals (RP) is a clinical CRO offering a wide range of clinical research services to provide clients with access to excellent study sites and experience in 15+ therapy areas. RP staff has broad experience in CRO services for phase I.-IV. biopharmaceutical trials, medical device trials and home care clinical studies. RP’s dedicated team gained strong industry expertise working at large pharmaceutical, biotech and CRO companies. RP’s leadership believe that the new way of serving market needs increases efficiency that leads to a victory for all participants – from sponsor to patient. RP bounds up with 150 associated staff – including research nurses. RP is fully dedicated to the highest standards of conducting clinical trials by CenterWatch SOPs and its trial activities are covered by HDI Insurance Services. The combination of local knowledge, global experience, and the latest technology allows our clients to conduct their studies faster and more cost-effective.
International Drug Development Institute (IDDI) is a therapy-focused expert organization in biostatistical, clinical data management and integrated eClinical services that is committed to assisting pharmaceutical, biotech, medical-device and nutrition companies, as well as academic institutions, in several disease areas, including oncology and ophthalmology. IDDI optimises the clinical development of drugs, biologics and devices thanks to proven statistical expertise and operational excellence.
Our services include Study Design, randomization and trial supply management (RTSM), Electronic Data Capture (EDC), Clinical Data Management, Biostatistics, Independent Data Monitoring Committees (IDMC), Biomarker validation and Personalized medicine.
Our experience amounts to 1200+ clinical trials (Phase I – IV), 850+ Scientific publication, 750+ scientific conferences and 350 happy customers. Science is part of our DNA.
Founded in 1991, IDDI is privately-owned, counts 150 employees and has offices in Belgium, and Raleigh (NC).
CC Clinical research Consultants is a clinical and regulatory affairs CRO (Contract Research Organization), based in central Paris, that provides clinical trials support to the Medical Industries throughout Europe. Assignments include regulatory and ethical initiation, full study management and monitoring, safety reporting, per European and local country requirements. Monitors assigned to a project are experienced, local country language speakers, and are located in or close to the assignment locations.
Industry experience of the upper management allows adequate understanding of clinial development needs, startup specificities, medical device particulars, regulatory requirements, teamwork and network building needs, deadline settings as well as budget implications and constraints.
Flexibility is a key feature of this medium-sized CRO, enabling adaptation to specific needs through direct interaction between the management of the CRO and the Sponsors and KOLs.
vivo Science is a Contract Research Organization located in Germany performing standard rodent toxicology and is specialized in immunogenetic and immunotoxicology studies. All studies are either Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) compliant depending upon the specific requirement.
Our experience is with the biopharmaceutical industry and large molecules as well as with small molecules. The study and report design are appropriate for submission to the pharmaceutical regulatory agencies. We also have experience in studies as described in the new European REACH guidelines for submission to the appropriate authorities.
It is our objective to assist our clients in determining the safety of their compounds as can be demonstrated using the rodent models. We work in close cooperation with our clients in designing the best means addressing both the standard toxicological as well as the immuno-toxicological aspects.
Anagram does clinical research since 1998, with Investigational Products and Medical Devices, from first-in-human to post-registry studies. With experience in most therapeutic areas we are highly specialized in Cardiology, CNS (stroke) and Oncology. Our 20 years’ experience with medical device (MD) clinical trials, have positioned Anagram as a leader in this area (MD and diagnostic kits).
Anagram and IEC merged in 2018 and provides integrated full service CRO + Imaging Core
lab services relating to:
DM & biostatistics
Medical Imaging core lab services (IEC)
We have extensive experience working with small / medium sized clients, who need advice and close support to design, plan and run their clinical research projects. While we work at international level, our main expertise is in Spain, where we provide high quality data with a cost effective and efficient approach. Our imaging Core Lab provides central reading and imaging analysis pertaining to patients in clinical trials, providing high quality data which can be directly exported to the eCRF.
Over 30 years of experience in managing medical device clinical investigations around the
Regulatory and quality experts to get medical devices registered rapidly and efficiently. Regulatory strategy development
Because medical device clinical investigations are highly specific, our team of experienced, (para)medically and multilingual monitors and project managers are exclusively dedicated to medical devices and work according to our certified ISO 9001 quality system while taking into account cultural nuances to save you critical time and resources for clinical investigation management throughout Asia, Europe, South America and the Middle East.
Our services are Global clinical strategy development including reimbursement, Clinical Evaluation Report writing, Protocol design and development including statistics, Investigator brochure writing, Instructions for use, CRF development, Site selection, Clinical trial agreements, Regulatory and Ethics Committee submissions, Clinical project management, Product training, Site monitoring, Medical monitoring – Safety reporting, Clinical report writing, Data management and biostatistics, Clinical auditing.
Aesculape CRO is a small CRO with presence in Europe and Asia. We have offices in Belgium, Spain, Italy, Poland, Hungary, Singapore, Malaysia, India, Thailand, Vietnam, Indonesia and the Philippines. We are offering full services (with subcontracting DM activities) in most therapeutics domains (Oncology, CNS, Cardio metabolic, ID, NCE, Biosimilars, medical devices, nutraceuticals)
MDX Research is a small CRO operating in Romania and Hungary.
Our in-house specialists are able to perform trial design, regulatory submission, site management, medical writing, data management and statistics.
We maintain strong relationships with Key Opinion Leaders in Romania and Hungary in varied therapeutic areas, oncology included.
In 2019 we obtained certifications in ISO 9001:2015, ISO/IEC 27001:2013 and ISO 14001:2015.
MDX Research designed and managed projects with drugs and medical devices. We
covered therapeutic areas such as oncology, diabetes and metabolic diseases,
cardiology, infectious diseases, ophthalmology, aesthetics and gynaecology.
Our dedicated people will perform medical content development, medical illustration included. We acquired extensive experience in life sciences and visual communication.
Our team of skilled medical translators are creating various kinds of documents in English, Romanian, Hungarian, Spanish and Serbian.
We’ll assist our partners with the development of scientific manuscripts, abstracts and conference posters. Our services include writing, micro-editing and referencing of medical documents.
Our partner institutions have GCP trained specialists.
MEDEX is an organization that specializes in managing clinical research sites. We provide services for Contract Research Organizations (CRO’s), pharmaceutical companies, biotechnology companies, and medical device companies.
Clinical trials frequently fail to reach its aim by reason of insufficient enrollment, poor compliance and performance. Proactive approach to site management is therefore a cornerstone of a clinical trial.
Site Management Services from MEDEX take the burden off investigators so that they can focus on the patient, and ensure that the study is conducted at the highest standards of quality, ethics and performance.
Poseidon CRO has a unique in class geographical coverage including North Africa,
Western Balkans and Hungary. We have an extensive network of collaborating sites and
maintain a solid relationships with Key Opinion Leaders in all our regions. This is
allowing us to perform all kinds of clinical trials, health market research studies,
Outcome Research, patient support programs and pharmacoeconomics.
Our comitted team has a strong knowledge in regulatory processes and clinical operations and is used to manage efficiently the most complex and demanding trials, thanks to a continuous improvement policy, embedded since the start in the companie's culture. We gained experience in various therapeutic areas such as oncology, diabetes and metabolic diseases, cardiology, respiratory, central nervous system, infectious diseases, ophthalmology, gastroenterology and gynaecology.
Our team is also providing medical translation of content allthrough the drug/medical device life cycle in English, French, Serbian, Arabic and Hungarian.
We are multinational CRO and covering Caucasus Region and particularly Georgia as the most desirable country to conduct Clinical Trial due to the fact that Georgia is well-known in the world where Approval to conduct Clinical Trial from the Ministry of Health’s Drug Approval Agency has maximum timeframe to issue Certificate of Approval within 21 days. However, as we have long term excellent relationship with the Regulatory Agency of the Georgia, in our experience we have had obtained Approval within two weeks.
Our Investigational Site network under our direct management have conducted numerous Clinical Trials and many of them have past FDA inspection with “Thank You” letters as there were no issues found and everything was in compliance with ICH/GCP.
Our company has Northern American headquarter in New York city (Manhattan) and European headquarters in the country of Georgia.
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