Medical Writing
From Concept to Approval: Comprehensive Medical Writing Services - The Write Choice!
Our flexible medical writing services cater to all your needs, from single projects to comprehensive solutions. Our expert team leverages their extensive experience in the pharmaceutical industry and academia, across a range of therapeutic areas and product types, to create impactful regulatory documents and scientific publications.
We partner with you from the earliest stages of trial planning, providing support with protocol outlines, to the final approval process by delivering a complete suite of Clinical Trial Documentation (CTD) compliant submission documents, all within deadlines. Our focus is on delivering high-quality, well-structured content that accurately conveys your message, while saving you both time and resources.
Our On-Point Medical Writing Solutions:
Protocol Development
Study Design Consultation
PK/PD
Reports
Clinical Summary Reports
Abstracts, Posters & Manuscripts
Editorial Support
Journal/
Conference Submission
Product Website Content
Educational Materials
Medical Marketing Reviews & Reports
Literature Reviews
Publication Planning
A Team of Medical Writing Pros, Dedicated to Your Success:
Comprehensive understanding of regulatory requirements and guidelines
Experienced medical writers with extensive knowledge in various therapeutic areas
Tailored writing solutions for each stage of the clinical development process
High-quality documents that meet regulatory standards and support study success
Streamlined writing process for fast, reliable and efficient delivery
Effective collaboration with study teams, stakeholders and regulators
Customizable writing solutions for complex and challenging projects
Use of cutting-edge technology to enhance accuracy, efficiency, and consistency
Access to a global network of writers, editors, and reviewers
Commitment to providing high-quality, cost-effective and timely services
Medical Writing Services in Nutshell:
- Develop study-specific style guide and templates.
- Contribute to study protocol development and submission.
- Develop informed consent forms and patient-facing materials.
- Write and compile study-related training materials.
- Assist with submission of ethics and regulatory applications.
- Provide input and review of study-related clinical and statistical reports.
- Write clinical study reports and manuscripts.
- Prepare interim and final study reports.
- Prepare summary reports for regulatory submissions.
- Contribute to clinical study data presentations and posters.
- Provide input and review of safety reports and clinical study updates.
- Prepare and compile clinical study appendices and attachments.
- Write and compile final study reports.
- Prepare manuscript and abstracts for publication.
- Provide support for regulatory submissions and interactions with regulatory agencies.
- Prepare and compile clinical study appendices and attachments.
- Contribute to post-study evaluations and assessments.
- Prepare post-study reports and presentations.
Case Studies.
Adding value to your businesses through our services
Other Expertise.
Regulatory Support Services
Project Operations
Clinical Data Management
Biostatistics
