A specialty pharma needed to determine the likelihood, with expected cost/timeline, that their new drug-device combo product will be reimbursed in Germany.
bizi engaged a German HTA expert and conducted a thorough review and analysis of prior HTA and reimbursement practices for the therapeutic area in Germany, including the ‘additional benefit assessment’ by G-BA and IQWiG.
Information and analysis included: how products obtain reimbursement, the pathway to achieving that, and a specific examination of how similar or competing products for the same indication achieved reimbursement and the data required of them. The analysis results were further validated through local KOL interviews.