Aava Biomed
Scientific and medical writing for regulatory, publication and communication needs
Aava Biomed, LLC translates complex clinical and preclinical data into clear, scientifically rigorous documents for regulatory, research and healthcare audiences.
Services
Medical writing across the clinical development lifecycle, from protocol to publication.
Clinical trial documents
Protocols and amendments, clinical study reports and synopses, and clear, participant-facing informed consent forms
FDA submission documents
Documents for IND, NDA and BLA submissions, such as:
- Clinical summaries and overviews (CTD Module 2.5 and 2.7)
- IND annual reports and Development Safety Update Reports (DSURs)
- FDA meeting briefing documents
- Responses to FDA information requests
Scientific publications
Peer-reviewed and congress publications based on clinical trial and real-world data, such as:
- Original research manuscripts and review articles
- Conference abstracts and posters
- Oral and slide presentations
- Literature reviews
Medical communications
Clear scientific narratives for research and healthcare audiences, including slide decks, white papers, plain-language summaries and medical affairs materials
Review and editing
Scientific review, quality control and editing of regulatory documents, manuscripts and other scientific content
About
Dr. Dikshya Bastakoty
PhD in Biomedical Sciences, Vanderbilt University
Aava Biomed, LLC is a Texas limited liability company and medical writing practice founded in 2024 by Dr. Dikshya Bastakoty.
Aava Biomed provides regulatory writing, scientific publications and medical communications across a range of therapeutic areas, working with clinical, regulatory, biostatistics and medical affairs teams to turn complex data into clear scientific narratives.
Contact
For project inquiries, please email:
contact@aavabiomed.com