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If you do business in the European Union, you’ll want to review this important content.

TÜV SÜD expert Dr. Bassil Akra discussed new medical device regulations on the clinical evaluation process for manufacturers and cover:
1. Current clinical data requirements in Europe
2. Common pitfalls during the preparation of clinical evaluation reports
3. Impact of new European medical device regulations
4. Helpful methods to avoid unneeded high clinical research costs
5. Keeping your time-to-market plan realistic

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