Sponsors
Wearable technology is increasingly being used as the new standard for objective outcomes in clinical trials. CamNtech provides a range of innovative miniature wearable recorders and dedicated analysis software for physiological monitoring.
The MotionWatch 8 is the smallest and lightest waterproof Actigraphy device currently available leading to very high patient compliance. Outcomes include sleep, circadian rhythm and physical activity levels. Where subjective data is important, our PRO-Diary offers the ability to capture Patient Reported Outcome on a unique, wrist worn eDiary synchronous with Actigraphy. Our integrated cloud data management system (CDM) provides a secure and robust data collection and management platform. Quality is paramount and CamNtech has full ISO13485:2016 certification, our products are CE marked and US FDA cleared. Our products are backed up by our worldwide network of distributors and supported from our manufacturing base near Cambridge UK and our offices in Boerne TX, USA.
Beijing Clinical Service Center (BCSC) isn’t your run-of-the-mill CRO.Founded 10 years ago, we have transformed from our humble beginnings as a local CRO into a national corporation working on everything from Pharmaceuticals to Medical Devices, through all phases of development.At BCSC we believe that the best healthcare should be available to everyone, everywhere. And that is why we have made it our mission to find companies like yours, with new and improved products, and help bring them to one of the largest markets in the world as soon as possible – China.Reach out to us for a consultation, find out which regulatory route your product should take, which Sites and Investigators you should approach, and how BCSC can help make your plans a reality.
CROMNIA has been established in 2009 as a contract research organization (CRO) in Izmir, Turkey. CROMNIA has a wide scope in the management of Phase II – IV of clinical and observational research projects in all therapeutic areas and supports Phase I studies in collaboration with Phase I Units of Medical Faculties. CROMNIA has experienced staff to effectively manage a clinical trial on time and on budget with success, and provides the services; Investigator contract, site initiation, clinical monitoring, Trial Master File management, vendor management, drug distribution management, close communication and cooperation both with study site and customer. Feasibility study is one of the key factors for success of a clinical trial. CROMNIA has a comprehensive site selection and feasibility strategy to avoid any risks. CROMNIA have skills for medical writing, medical translation, site coordinator services and investigator meeting organization.
Institute for Medical Research (IMR) is the first private institute for medical scientific research in Bulgaria. It provides consultation, expert services and solutions based on innovation and technologies in the field of medicine, biotechnology and business. Relying on knowledge, experience and competence, IMR develops its activities in four directions: “Personalized medicine”, “Clinical Trials”, “Scientific Programs/ Projects” and “Health Technology Assessment”, and builds individual concept for each separate client/ project. Acting as a CRO, IMR offers a full service spectrum for clinical trial design and conduction, as well as for validation studies and scientific projects, including: pre-study research, study design, start-up phase modeling and organization (regulatory submission, site contractual negotiation, payment process, etc.), project management, monitoring, data management and statistical analysis, final study report preparation. Company’s services and activities are in full compliance with ICH guidelines, GCP standard, local regulatory requirements and IMR’s/ client’s SOPs, guaranteeing its reliability as a partner.
Milray MC is a local CRO providing a well-tested full-service for the conduct of clinical trials in Republic of Moldova. We are young company but have a team of well-trained specialists according to the GCP requirements. Moldova has a population of ~3.6mln, a centralized healthcare system, dedicated doctors with experience in CT and friendly patients motivated to collaborate. The organization of healthcare in Moldova channels patients into a small number of specialized centers, from which they can be selected and treated at the same site. We can cover all main therapeutic areas through our established network of doctors in main hospitals of the country. We know in detail all local RA requirements for CT approval and are flexible in ensuring the success of the trial.The prices of Milray MC are more attractable compared to European CROs, for all performed CTs in Moldova.
SYNLAB pharma institute offers a very broad range of laboratory services to the biotechnology and pharmaceutical industries as well as to manufacturers of medical devices and novel foods. SYNLAB pharma institute is a division of the SYNLAB group. Headquartered in Germany, the SYNLAB group is the leading provider of diagnostic services in Europe with more than 300 laboratories in 35 countries.
Click to Read More SYNLAB pharma institute supports the complete drug life cycle from research and development, through preclinical and clinical studies to release and manufacturing of the final product. Our clients take advantage of our large spectrum of analytical methods for development programs and drug production, supported by our global logistical capabilities; always working in accordance with the highest standards such as ISO 17025/15189, GMP, GLP, GCLP or GCP.
Take advantage of over twenty years of analytical expertise and our extensive experience gained from supporting more than 3,000 clinical trials and projects.
As an international active CRO we have operated clinical trials in over 15 countries. In 25 years, we have successfully run more than 250 clinical trials and non-interventional studies. Our clients range from Big Pharma to Biotech, Diagnostics and Medtech companies. Our experienced team with an average of >12 years in clinical research span a wide range of indication knowledge: Oncology, hematology, cardiovascular, CNS, respiratory and various inflammatory diseases.
We cover all aspects of clinical research:Click to Read More
– Clinical operation (International PM, remote and on-site monitoring)
– Feasibility and Site Selection
– Regulatory
– Safety & Vigilance
– Medical Writing
– QA Services
– Data Management/Statistics
Our very own CTMS portal software accSIS offers our customers at any time a perfect control and broad overview on any key aspect of the study. Whether a registry study at a single site or a multinational trial, we are always highly focuses on the project progress, meaning fast response times, open communication and high flexibility.
TCRS is a boutique CRO providing a full range of clinical development services to biotech, pharma, and academia Our background in Hospital Research Management gives makes us uniquely qualified to work with clinical teams and has enabled us to successfully deliver studies across the world With a highly developed network of contacts in the UK healthcare system and intimate knowledge of individual hospitals, we are ideally qualified to select and manage the very best UK sites for your study. Click to Read More
And our hands-on experience of the NHS infrastructure means we can deliver ultra-rapid study start-up by expertly managing the regulatory, ethics and hospital approval process. Following extensive consultations with Regulators and Government bodies we have taken concrete actions to ensure we are fully prepared for ‘Brexit.’ Whether you are seeking full support for every aspect of your clinical development programme or just for one part of a study, TCRS offers flexibility, momentum and value.