Regulatory, Scientific & Medical Writing

Partner with an experienced, scientifically driven team to support your program’s success

Drug development requires effective, highly technical communication across all program phases. TD2 can support your program with comprehensive, high quality writing services. Our experienced team of scientific, regulatory, and medical writers have deep Oncology experience and knowledge to deliver documents and quality content that are critical to your program’s success.

Regulatory Affairs

TD2’s Regulatory Affairs and Translational Research Team engages Oncology drug development experts and strategists with proven track records of success. We leverage experienced, oncology-focused medical writers, regulatory experts in CMC, pharmacology, and toxicology, as well as regulatory program managers to provide a customized approach across all areas of drug development.

Learn more about our Regulatory Services.

Contact our experts to help advance your development program with our trusted translational regulatory consulting team.


Get Started.

Have questions about how TD2 can assist with your regulatory needs? Reach out to our expert staff today to get started.