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Professional Services for Clinical Trials

Clinical trial professional services for confident trial delivery

Wemedoo's professional services combine clinical research expertise across multiple disciplines. We help teams design, align, and operationalize trials with clarity, consistency, and control.

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Trial Design & Medical Writing

Clinical trial design, protocol development and medical writing

Wemedoo provides expert support across clinical trial design, protocol development, and medical writing, including informed consent forms, lay summaries, clinical study reports, and regulatory submission documents. Our multidisciplinary teams combine clinical, statistical, and regulatory expertise to deliver submission‑ready documentation aligned with ICH GCP, FDA, EMA, and global regulatory requirements.

Biostatistics & Statistical Programming

Biostatistics services and statistical programming

Biostatistics and statistical programming services support clinical trials from study design through regulatory submission. By applying validated analytical methods and generating CDISC‑compliant SDTM and ADaM datasets, these services deliver reliable, submission‑ready outputs aligned with FDA, EMA, and global regulatory expectations.

Clinical Data Management

Clinical data management services

End‑to‑end clinical data management services support trials from CRF design through database lock, ensuring data accuracy, traceability, and regulatory compliance at every stage. With structured data processes, real‑time validation, and risk‑based oversight, these services enable faster database lock and inspection‑ready datasets.

Clinical Trial Software

Power your studies with unified clinical trial software

Unified clinical trial software that brings together data, workflows, and oversight across the entire study lifecycle. By connecting core trial functions within a single environment, teams gain real‑time visibility, reduced fragmentation, and stronger alignment between clinical, operational, and regulatory activities.

Our Clients

Who we work with

We work with a wide range of organizations and research models, supporting different study types, therapeutic areas, and client needs

Clinical trial types

We support a wide range of clinical trial designs, from early-phase and decentralized studies to complex, multi-site programs

Therapeutic areas

Expertise is provided across various therapeutic areas, addressing differing data requirements, workflows, and regulatory expectations

Our clients

We work with sponsors, CROs, academic institutions, and research organizations with varying structures and operational models

Trusted partners

Global network of partners

Mediri
Appletree CI Group
Across Global Alliance
Ad Hoc Clinical
Akshar Global Clinical Research
Axiom
Centinel Spine
Costello Medical
Gaea OU
GCT
Lumen Bioscience
Martifarm
Oxular
Polpharma
Proxima
Pykus Therapeutics
Research Professionals CRO
Swiss Cancer Foundation
University Hospital of Bern Inselspital
Velocious Clinical Research
Worwag Pharma
ZAK Clinical Research Services

Get in Touch

Ready to strengthen your clinical trial execution?

From study design to submission, our professional services provide the expertise and structure needed to move your trial forward efficiently

Talk to our team

Frequently asked questions (FAQ)

What do Wemedoo's professional services cover?

Wemedoo's professional services support clinical trials across key areas including trial design, protocol development, medical writing, biostatistics, statistical programming, and clinical data management. Services are designed to help teams plan, align, and deliver trials efficiently and in compliance with global regulatory requirements.

At what stage of a clinical trial can professional services be engaged?

Professional services can be engaged at any stage of the clinical trial lifecycle, from early study design and protocol development through data management, statistical analysis, and regulatory submission. Teams often engage services early to establish strong foundations and reduce downstream delays.

Who can benefit from Wemedoo's professional services?

Services support a wide range of clinical research organizations, including biotech and pharma companies, CROs, academic institutions, and research networks. They are adaptable to different study sizes, therapeutic areas, and organizational models.

How do professional services support regulatory compliance?

All services are delivered in alignment with ICH GCP guidelines and relevant regulatory frameworks such as FDA and EMA requirements. This includes the production of submission‑ready documentation, CDISC‑compliant datasets, and inspection‑ready data and processes.

Can professional services work alongside existing systems and vendors?

Yes. Professional services are designed to integrate with existing systems, vendors, and processes. Teams can leverage expert support while continuing to operate within their preferred technology and operational setup.

How do professional services and clinical trial software work together?

Professional services and unified clinical trial software are designed to complement each other. Services provide expert planning, oversight, and execution, while software supports connected workflows, data visibility, and operational consistency across the study lifecycle.

How can teams get started with professional services?

Teams can start by discussing their study goals, timelines, and challenges with Wemedoo's experts. This helps identify the right mix of services to support efficient trial delivery from design to submission.