Apices’ team can assist with any process involving medical writing, staffed as it is by a wide range of highly qualified professionals ‒ including scientific directors, medical writers, medical editors, therapeutic area team leaders, and publication support specialists.
We are committed to playing a key role in helping companies submit regulatory documents as part of both the drug development process and the publication plan. Apices’ medical writers are trained in research methodology and have substantial experience with medical publications. Working closely with first-line specialists in therapeutic areas, they can provide the ideal combination for success ahead of congress communications, allowing enough time to develop and submit abstracts, posters and/or oral communications.
Apices’ medical writing and communication services include:
- Clinical study protocols, patient information sheets and informed consent forms
- Investigational medicinal product dossiers
- Abstracts and posters (including their submission to congresses)
- Clinical study reports
- Oral presentations
- Manuscripts and journal papers (including submitting them to journals and posting responses to reviewers)
In addition to the above, we offer support with submitting documents to congresses and journals, as well as preparing responses to reviewers, following the templates and characteristics provided by the medical journal/congress and in line with International Committee of Medical Journal Editors (ICMJE) recommendations and the elements of the relevant reporting guideline (eg. Consort Statement).