MARKET ACCESS-RELATED DOCUMENTS

CHEMISTRI

We take the lead in the writing up, lay outing and structuring of reimbursement dossiers to be submitted to the Belgian and Dutch authorities, based on a variety of source documents (clinical study reports, global value dossiers, published and non-published sources).

In addition, we can help the market authorisation holder with the preparation and submission of additional risk minimisation activities or measures (RMA or RMM) materials conform the national guidelines.

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