Regulatory assistance for clinical trials

CROss Alliance™ experienced staff prepares and presents the Clinical Trial Application (CTA) package to gain regulatory approval for clinical studies from the relevant Ethics Committee and Central Agencies in Switzerland and all Europe.

After study completion, our group has in-house skills and background experience to support our Sponsors in answering all the questions related to the performed clinical part that may arise from Regulatory Authorities throughout the marketing authorization process.

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All the “pathways” to get in touch with CROSS. Feel free to contact us for any additional information you may need, we will be glad to assist you in the shortest time possible.

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