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Team of Experts Dedicated to Medical Writing

Clear, compliant, and compelling medical documents to accelerate your clinical and regulatory success.
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At every phase of your product's lifecycle, our medical writing services align with your objectives, ensuring each document meets the requirements of regulators, healthcare providers, and patients. Innovation and reliability are at the core of our service.

From Concept to Pre-Clinical Preparation
From Concept to Pre-Clinical Preparation
Begin your journey with our comprehensive medical writing support designed for the discovery phase of drug and medical device development. Our services include creating detailed discovery reports, pre-clinical study protocols, and literature reviews to provide a strong foundation for your clinical trials. We help define the scientific rationale, mechanism of action, and potential therapeutic benefits, setting a clear path towards regulatory approval. Documents prepared in this phase:
  • 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
We offer comprehensive solutions for the post-marketing phase, including periodic safety update reports, post-marketing surveillance reports, and patient education materials. Our team ensures your documentation meets regulatory requirements, supports product optimization, and enhances patient outcomes in real-world settings. Documents prepared in this phase:
  • 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

Medical Writing Service Process

The typical process of medical writing is divided into a clear process:

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 focus on the unique needs of the healthcare, pharmaceutical, and biotech industries worldwide. We don't just translate content; we create and adapt it in multiple languages, ensuring the final output is as impactful as the original version.

01
Expertise

Our team of content creators and copyeditors comprises highly skilled professionals with specialized expertise in the life sciences and extensive experience in multilingual content creation. Each editor brings a deep understanding of the scientific nuances necessary for accuracy and the linguistic finesse required for clear, persuasive communication. Fluent in multiple languages, they ensure that each piece of content meets the highest standards of grammatical and stylistic excellence while resonating with cultural authenticity and relevance. With a keen eye for detail and a commitment to precision, our copyeditors refine and enhance your content, ensuring 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 with 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 high-quality, ready-to-publish content.

Why Choose Willingjet

20 Years of Experience

Our team consists of seasoned medical writers, each with specific expertise in 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 Expertise

We stay 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.

Flexible Solutios

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
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