/ Technical Writing
Technical & Medical Writing Services
Accelerate your scientific and medical research projects with PhD expert technical writing services.
From IND applications to clinical trial reports, our medical writing services will help streamline your technical documentation and reduce time-to-market.
Keep your regulatory programs and technical projects on track with precise, high-quality writing that supports your development programs. Navigating the complex regulatory landscape can be overwhelming, with high-stakes documentation that requires absolute clarity. While your team is focused on the science, preparing the extensive regulatory or technical documents can become a time-consuming burden, with just one misstep delaying or hindering submissions. Don’t let documentation slow down your progress.
At Co-Labb, we support biotech and healthcare companies by handling the writing of technical and regulatory documents, ensuring accuracy and compliance. With our PhD-level team of technical writers, you can focus on innovation while we streamline timelines and reduce your documentation workload. Whether it's IND applications, clinical protocols, or whitepapers, we deliver expert medical writing services to keep your projects on track without compromising quality.
That’s why Fortune 500 companies trust Co-Labb to deliver technical & medical writing services that support their success and accelerate time to market.
Client Testimonial
"Co-Labb supported us in an effective way by quickly understanding our brief and delivering documents quickly with good communication along the way."
Gaëlle Briand
Baxter Fluid Management Marketing Manager
We assist companies in advancing their development programs by offering writing support throughout the IND and NDA/BLA pathways. From FDA INTERACT and Pre-IND briefing packages, to full IND submission support.
Regulatory Writing
As one of the top medical writing companies our expertise spans multiple areas of healthcare and medical projects, including clinical trial protocols, informed consent forms, Institutional Review Board (IRB) applications, clinical study reports, and standard operating procedures.
Medical Writing
Our medical technical writers also support startup companies at the nonclinical stage, ensuring their IND-enabling animal studies are properly documented through nonclinical study protocols, SOPs, and study reports.
Technical Writing
Our fully hands-off manuscript writing service delivers your research to the world with impact, supporting regulatory filings, investor communications, and grant funding. For more details, visit our manuscript writing page.
Manuscript Writing
Ideal for presenting research to technical audiences, such as investors or funding agencies, or for marketing your product upon market entry. Our scientific writing and communication experts excel in the end-to-end creation of whitepapers, offering strategic planning, and skilled writing.
Technical Whitepapers
Expert Scientific and Medical Writing Services for Every Stage of the Development
Technical Writing Case Studies
We are a results-driven technical & medical writing agency that isn't afraid to back up our claims. Explore our case studies to see the real-world impact our technical writing services have made for global brands.
“Co-Labb has been a great resource for us at Genomics England. They've supported us with scientific papers, whitepapers, and presentations, quickly understanding what’s needed and delivering clear, engaging content from complex material with minimal guidance. Working with Co-Labb feels like collaborating with knowledgeable partners who truly care about the work.”
Alexander Renziehausen
Head of the Science and Clinical Office
Testimonials
Our Road Map to Your Medical Technical Writing Success
With Co-Labb’s writing expertise, you can focus on your core research and development efforts while we support your documentation needs. Our structured, collaborative process ensures your technical and regulatory documents are accurate, compliant, and delivered on time.
1
Initial Consultation
We begin by working closely with your in-house experts to understand the specific goals and requirements of your project. Whether it's preparing regulatory submissions, clinical trial documentation, or technical reports, this step ensures we align our approach with your objectives and industry standards.
2
Drafting & Content Development
Once the structure is in place, our PhD-level team of medical technical writers begin drafting your technical documents. Whether it’s an IND application, clinical protocol, or nonclinical study report, we ensure your data is presented with clarity and precision.
3
Internal Quality Control Review
Every document undergoes a rigorous internal review by a second member of our team to ensure accuracy and clarity. This quality control process ensures that your documents are well-organised, easy to understand, and meet the highest standards.
4
Client Review & Feedback
We value collaboration, and your input is essential. After the internal review, we provide the draft to your team for feedback. We incorporate your insights and ensure that the final document meets your expectations and aligns with your internal objectives.
5
Final Revisions & Submission Preparation
Once the documents are finalised, we ensure that they are submission-ready by formatting it according to relevant guidelines, whether for regulatory bodies or internal use. If needed, we can also assist with the submission process, ensuring all elements are in place for timely and successful review.
Are You Ready to Elevate Your Content?
Book a free 30 minute project discovery call
Let’s turn your ideas into impactful results. Book a 30-minute discovery call today, and let’s explore how we can help you achieve your goals with our specialist writing services.