
Research and Briefings
Impending Changes to the EU Medical Device Regulations
New EU medical device regulations will begin coming into force from April 2020.
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XA global team of industry specialists can help life sciences companies map out risk management strategies and tactics as new issues — and opportunities — emerge.
Drug development and marketing. Pricing challenges amid health care reform. Breakthrough health discoveries and “fast track” approvals. The continuing growth of generics and emerging biosimilars. A complex and evolving global regulatory environment. Amid this dynamic and ever-changing business climate, Marsh’s life sciences industry experts develop and implement strategies tailored to your unique needs.
Among our areas of specialty:
By helping reduce your total cost of risk with tailored solutions — insurance brokerage, advisory, and risk management services — Marsh can help you minimize the volatility and severity of risk, protect assets, and maintain profitability.
For clients across the global pharmaceutical industry — biopharma, specialty drugs, generics, animal health, and nutraceuticals — Marsh offers solutions that include:
For clients across the global biotech industry — from large global enterprises to small specialty and “incubator” firms — Marsh offers solutions that include:
For medical device manufacturers, diagnostics companies, and consumer health aid product marketers, Marsh offers solutions that include:
For life sciences service providers — wholesale distributors, research institutes, contract manufacturers (CMOs), and contract developers (CDMOs) — Marsh offers solutions that encompass: