Quality
With our extensive experience and proven track record, our team guides you to clearly visualize the quality of your project before implementation.
Our TEAM
Our team is comprised of MD and PhD holders with over 15 years of experience in the Western pharmaceutical industry, providing expert support.
Speed
Leveraging our extensive experience and proven track record, we build the shortest delivery schedules and foster seamless communication throughout your project.
Global
Our global team, located in countries like the U.S., UK, Japan, India, Thailand, Singapore, and Canada, delivers high-quality work with a global perspective.
Technology
To continuously enhance our service quality, we actively integrate cutting-edge technologies like AI and big data analytics.
Flexibility
Our processes are adaptable, allowing us to customize workflows to perfectly match your unique circumstances and Standard Operating Procedures (SOPs).
In an era where healthcare decisions are increasingly data-driven, Real-World Evidence (RWE) has emerged as a crucial tool. It helps us understand patient outcomes beyond controlled clinical trials, drawing on past data to guide future diagnoses. This means more patients receive appropriate treatment, leading to optimized healthcare costs, fewer errors, and improved quality of life.
RWE is gaining global importance because it complements clinical trial data, fills evidence gaps, and translates clinical trial evidence of drug efficacy and safety into real-world effectiveness, safety, and tolerability. Its relevance in regulatory, market access, and clinical decisions continues to grow.
To learn more about Real-World Evidence, we can send you a detailed document. Please fill out the necessary information in the [Contact Us] section below and indicate "RWE Document Request" in your message.
Assemble a dedicated team tailored to your specific project
At Medpro Clinical Research, we form a "Professional Team" tailored to your project, drawing from our 20+ experienced writers and editors.
We swiftly deliver high-quality support for medical and product strategies, clinical research (including trials and RWE), and all writing needs.
Long-Term Support
At Medpro Clinical Research, we support both short-term projects, like native English checks, and long-term projects spanning years.
For extended engagements, we assign dedicated writing team members to ensure continuous support. We take full responsibility for your project from initiation through publication and even handle post-publication inquiries.
Our Valued Partner: BIOVISER
BIOVISER, a key partner of Medpro Clinical Research, is a solutions provider for pharmaceutical and medical device companies.
They bring significant advantages in medical writing and analytical report generation, directly supporting Medpro CR's services.
BIOVISER recruits and trains top talent globally to meet client needs.
MedPro Clinical Research services have been powered by BIOVISER Group
Order Process
１．Contact
Please contact us via our inquiry form.
A representative will get back to you within 1-2 business days.
２．Meeting
To best understand your project, we offer consultations by phone, email, Teams, or Zoom.
Kindly provide us with your detailed requirements so we can better assist you.
３．Order
Upon finalization of your project details and contract signing, you can initiate your order.
Please don't hesitate to discuss payment arrangements that suit your needs.
４．Initiating Your Project
We'll assemble a team of our experts tailored to your specific project, then kick off the work.
We'll keep you informed with regular updates and meetings as we progress.
５．Delivery & Submission Complete
The timeframe for project completion varies depending on the project's scope.
Please feel free to contact us for delivery timelines and other details.
Variety of Services
Manuscript Submission
Support Service
We provide comprehensive manuscript submission support, ensuring your work is polished and ready for publication. Our services include English manuscript checks and style formatting, all handled by editors who hold PhDs in medical fields and possess over 10 years of experience in English proofreading.
We specialize in supporting the submission of:
✅ Clinical trial papers, clinical study papers, and review articles
✅ Database studies, real-world data analyses, and Post-Marketing Surveillance (PMS) reports
Scientific Publication
Our team of expert medical writers specializes in crafting high-quality English clinical research papers. With 10 to 20+ years of experience, we adhere strictly to essential publication guidelines such as CONSORT and ICMJE to ensure your work meets international standards.
We provide comprehensive writing support for:
✅ Primary and Secondary Publications
✅ Database Studies and Real-World Evidence Papers
✅ Abstracts, Conference Posters, and Presentation Slides
English Editing &
Proofreading Services
We proofread and edit a wide range of English documents for clinical research. This includes regulatory documents, manuscripts, conference posters, and white papers.
You can choose from three service options to best suit your needs.
✅ Language Check
✅ Editing
✅ Scientific Editing
Medical・
Writing
✅ Protocol writing
✅ Informed Consent
✅ CSR (Clinical Study Report）
✅ CER (Clinical Evaluation Report)
We write regulatory documents in accordance with ICH guidelines.
HTA / HEOR
Global Value Dossier作成
Systematic Literature Review
Meta Analysis
Evidence GAP Analysis
White Paper
We provide research and writing services to meet your project needs.
Clinical・
Operation
✅ First in man drug & device trials
✅ End to end management of phase II trials
✅ Site management of phase III trials
Pharmacovigilance
✅ Drug safety information
✅ Adverse event reports
We can create English documents and manage operations directly within systems like ARGUS and ArisG.
Reprint Service
✅ International Journal Reprints
We've partnered with a company that holds the copyrights for international journal reprints.
If you need reprints of articles published in international journals, please feel free to contact us.
New Services
✅ Flexible Service Implementation
At Medpro Clinical Research, we actively introduce new clinical research technologies and services from overseas.
We strive to meet your requests whenever possible. For any service inquiries, please feel free to contact us via our "Contact Form."
Business Partners
Pharmaceutical Companies
Medical Conferences
X (Twitter)
News/Columnを更新しました。
— MedPro Clinical Research (@ClinicalMedpro) October 16, 2025
「学会、Conferenceの準備について (2026年4月～分)」
記事はこちら☟https://t.co/ybkhk6UFPH