Services:

• Product Assessment
• Portfolio Evaluation
• Dossier Review
• Regulatory Process
• EU/USA Registration
• Market Research
• Licensing
• Finding Partners
• Strategy and Planning
• Fund Raising
• Due Diligence

Existing EU and USA Approvals for Registration in Central and East Europe, Russia and the CIS:

Companies wishing to register and market their products, whether pharmaceuticals or medical devices which already have regulatory approvals outside of these geographical regions frequently need guidance on how to proceed in these countries.

Before making strategic decisions and potentially significant financial decisions regarding market entry it is more cost effective to have MMA review the proposition and advise on both time lines to be expected and likely costs to be encountered.

MMA will conduct such reviews promptly and report comprehensively. For companies wishing to move forward following such a review MMA is able to manage the regulatory process locally.