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Expert Medical Writing That Transforms Research into Results

Crafting clear, compliant, and compelling medical documents to accelerate your clinical and regulatory success.
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At each stage of your product’s lifecycle, our medical writing expertise integrates seamlessly with your goals, ensuring that every document not only meets but exceeds the rigorous demands of regulators, healthcare providers, and patients alike. Partner with us to ensure that your documentation is as innovative and reliable as your products.

From Concept to Pre-Clinical Readiness
From Concept to Pre-Clinical Readiness
Kickstart your journey with comprehensive medical writing support tailored for the discovery phase of drug and medical device development. Our services include the creation of detailed drug/device discovery reports, pre-clinical study protocols, and literature reviews to ensure a robust foundation for your clinical trials. We help articulate the scientific rationale, mechanism of action, and potential therapeutic benefits, setting a clear path towards regulatory approval. Documents prepared in this phrase:
  • Pre-clinical Study Reports

  • Pre-clinical Sections of INDs

  • Clinical Sections of INDs

  • Clinical Development Plans

  • Investigator Brochures

  • Exploratory Protocols

  • CTD Modules

Navigating Through Clinical Trials with Precision
Advance through the critical stages of clinical research with expertly crafted documentation that meets global regulatory standards. Our team provides end-to-end medical writing services including clinical trial protocols, patient information and consent forms, interim analysis reports, and final study reports. We ensure that all documents are clear, compliant, and ready to support both the conduct and reporting of clinical trials, facilitating smoother regulatory review and faster market access. Documents prepared in this phrase:
  • Investigator Brochures Updates

  • Clinical Trial Protocols

  • Informed Consent Documents

  • Annual Safety Reports

  • Clinical Study Reports

  • Patient Narratives

  • Clinical Trial Registry Synopses

  • Abstracts and Posters

  • Manuscripts

  • Patient Diaries

Navigating Through Clinical Trials with Precision
Supporting Market Success and Beyond
Supporting Market Success and Beyond
Continue to thrive in the post-marketing phase with our expert medical writing services designed to support ongoing compliance and market surveillance. We offer comprehensive writing solutions such as periodic safety update reports (PSURs), post-marketing surveillance reports, and patient education materials. Our team ensures that your documentation continues to meet regulatory requirements, supports product optimization, and enhances patient outcomes in the real-world setting. Documents prepared in this phrase:
  • Phase IV Study Documents

  • Abstracts and Posters

  • Periodic Safety Update Reports

  • Manuscripts

  • Slide Decks

  • Review Literature

  • Product Monographs

  • White Papers

  • Therapeutic Training Modules

  • Q & A Booklets

Typical Process

The typical process of medical writing includes the following steps.

Consultation and Planning
Consultation and Planning

Every successful project begins with a thorough consultation to understand your objectives and requirements. During this phase, we outline the scope, timelines, and specific needs of your project.

Development and Drafting
Development and Drafting

Our medical writers then craft the documents, integrating all necessary scientific and regulatory elements. We ensure each document is tailored to meet the precise specifications of your project.

Review and Revisions
Review and Revisions

Following initial drafts, our documents undergo rigorous reviews by senior writers and subject matter experts to ensure accuracy and compliance. We then work closely with you to make any necessary revisions.

Final Approval and Delivery
Final Approval and Delivery

Once the documents meet your satisfaction and our quality standards, we proceed to final approval. The completed, compliant documents are then delivered ready for regulatory submission or whatever next steps your project entails.

Multilingual Copywriting

Our multilingual medical copywriting services are designed to meet the unique needs of the healthcare, pharmaceutical, and biotech industries across the globe. Our service is designed not merely to translate but to create and adapt content directly in multiple languages, ensuring that the final output is as original and impactful as its source.

01
Team

Our team of content creators and copyeditors is a diverse group of highly skilled professionals with specialized expertise in the life sciences and extensive experience in multilingual content creation. Each editor brings a deep understanding of both the scientific nuances necessary for accuracy and the linguistic finesse required for clear, persuasive communication. Fluent in multiple languages, they are adept at ensuring that each piece of content not only meets the highest standards of grammatical and stylistic excellence but also resonates with cultural authenticity and relevance. With a keen eye for detail and a commitment to precision, our copyeditors play a pivotal role in refining and enhancing your content, ensuring that it achieves its intended impact on a global scale.

02
Workflow

The process begins with a detailed client consultation to understand specific needs, objectives, and target audiences. Based on this initial discussion, we assign a specialized team of content creators and copyeditors who have expertise in the relevant life sciences sector and proficiency in the target languages. Each project progresses through a structured sequence of content creation, where our writers develop original, scientifically accurate text. This is followed by rigorous rounds of editing and quality assurance to refine linguistic precision and ensure regulatory compliance. Throughout the process, we maintain continuous communication with our clients, incorporating their feedback and making adjustments as necessary. The result is a delivery of high-quality, ready-to-publish content.

Why Choose Willingjet

Unmatched Expertise

Our team comprises seasoned medical writers, each with specific expertise spanning across pharmaceuticals, biotechnology, and medical devices. With advanced degrees in life sciences and extensive regulatory knowledge, we transform complex scientific data into clear, comprehensive documents.

Regulatory Mastery

Navigating the maze of regulatory requirements is second nature to us. We pride ourselves on staying up-to-date with the latest guidelines from the FDA, EMA, and other regulatory bodies to ensure your documentation is compliant and positioned for success.

Tailored Solutions

We recognize that each client has unique needs. That’s why we offer customizable services that adapt to your specific project requirements, whether it’s a small-scale study or a large multinational clinical trial.

Timely Delivery

Meeting your deadlines is crucial. We commit to not only meeting but often exceeding timelines, ensuring that your project moves forward without delays.

ISO 9001
ISO 9001
ISO 17100
ISO 17100
ISO 13485
ISO 13485
ISO 27001
ISO 27001
ISO 14001
ISO 14001
ISO 28000
ISO 28000
Get in Touch
Ready to learn more about our Medical Writing services? Contact us today!
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