Functional Support Services
Dokumeds is a leading European Clinical Development solutions provider. We have 25 years of experience in the industry and we offer functional support services to cover the gamut of your clinical development and life-cycle needs.
Regulatory Affairs
Practice-based regulatory consulting expertise, and support throughout the product life cycle.
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Pharmacovigilance
We deliver high-quality solutions, with services designed to ensure patient safety at every stage of the drug life cycle.
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Feasibility
We have been Feasibility Specialists for over 20 years. Sponsors contact us for specialist regional feasibilities, and oversight of global feasibility studies
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Medical Services
Our medical team will nurture relationships with key leaders, from development until product launch.
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Start up Services
Expert-led planning and design processes that will keep the trial on-time and on-budget.
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Clinical Supply and Logistics Management
Cost effective local logistics chain for clinical trial supplies and laboratory samples.
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Other Functional Support Services
Contract Management
Dokumeds have extensive knowledge of local contracting (Legal , Clinical, Regulatory)
Payment Management
Our financial solutions allow you to meet your clinical study requirements easily
Medical Monitoring / Review
Our experience and knowledge allows us to solve your clinical study challenges within a wide range of therapeutic areas
Medical Writing
Our highly skilled medical writing teams are here to support you in developing medical and scientific documentation for your clinical studies
Enrolment Liaison Management
We manage relationships with sites to ensure full engagement throughout the course of the study
Medical Science Liaison
We provide skilled and connected Medical Science Liaison Managers who develop relationships with key opinion leaders (KOLs) and Doctors to effectively market your product
Outsourcing of Staff
We deliver on demand clinical research specialists to fit your needs
Quality Assurance
Our highly skilled Quality & Compliance team is ready to serve your clinical studies
Consulting
Our Clinical development and Regulatory consulting can help you get your trial off the ground
Our statistics
22
therapeutic areas
25
years in business
32
countries
Benefits
25 years of experience in the industry
Our extensive industry experience means that we've overcome every challenge imaginable. Our excellence in Clinical Research and Project Management is strengthened by this.
Feasibility study experts
Our feasibility studies are incredibly thorough and precise, minimising potential challenges so that you can take the next step with your trial.
Qualified and experienced team
Work with experienced and dedicated staff. Over 40% of Clinical Operations staff have an MD, and another 50% have a PhD, Pharmacy or Life Science education.
Transparent pricing
Stay on budget with our reasonable and transparent costs.
