Our services include providing regulatory and non-regulatory documentation as well as translations (from and to English, French and Dutch). Our documentation catalogue/portfolio ranging from clinical documentation, medical devices (user's guides, quality related documentation and regulatory documentation.
Instructions for use, clinical users guides, safety guides, application notes
Neuroscience, oncology, infectious diseases and vaccines
Veeva Vault, FrameMaker, Word, SharePoint, Adobe.
CSR, protocols, IMPD, narratives, clinical summaries. Translation of documents from to English, French and/or Dutch.
SOPs according to GDP, GMP. Translation of documents from to English, French and/or Dutch.
QC of documentation to align with customer's style guides. Proof reading and editing in English, French and/or Dutch.
T-Right has been opportuned to provide services for a range of customers, ranging from CRO's to small biotechs, large pharmaceutical companies in the USA, France and in Belgium.
While most of the document we delivered over the years are in English, documentation in Dutch also represents a small part of our portfolio. With more recent expansion, we are now happy to provide documentation in English, Dutch and/or French.



“Storytelling at its best. Even when it comes to pharmaceutical documentation” - Annelies V. (Director of Medical Writing)
Short Stay Lodging
Poetry Reading
Life/Career Coaching
Foot Reflexology
More info at T-Sole.be