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

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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.