Medical Writing
Our experienced medical writing team specializes in crafting clear, accurate, and compelling clinical documentation for global regulatory submissions. With a deep understanding of various therapeutic areas, we provide expert support throughout the entire drug development process, from early-stage clinical trials to post-marketing surveillance. Our expertise spans:
Regulatory Writing
IND/NDA Submissions: Preparation of Investigational New Drug (IND) and New Drug Application (NDA) submissions to regulatory authorities.
Clinical Study Reports: Drafting comprehensive reports summarizing the results of clinical trials.
Protocols: Developing detailed plans for conducting clinical trials.
Statistical Analysis Plans: Creating plans for analyzing clinical trial data.
Labels: Writing product labels and patient information leaflets.
Safety Updates: Preparing periodic reports on adverse events and safety data.
Scientific Writing
Journal Articles: Drafting scientific manuscripts for publication in peer-reviewed journals.
Conference Abstracts and Presentations: Preparing abstracts and presentations for scientific conferences.
Review Articles: Writing comprehensive reviews of the literature on specific topics.
Book Chapters: Contributing to books and textbooks.
Medical Communications
Patient Education Materials: Developing materials to educate patients about their conditions and treatments.
Healthcare Professional Marketing Materials: Creating materials to promote products to healthcare professionals.
Medical Device Labeling: Writing labels and instructions for medical devices.
Grant Writing
Research Grant Proposals: Preparing proposals to obtain funding for research projects.
Foundation Grants: Writing grant proposals to foundations.
Government Grants: Applying for grants from government agencies.