There are some things in life you want to be consistent and predictable. Interest rates. Train timetables. The weather. And if you work in the pharma industry, the FDA.

However, like leaves on the line or unexpected hail storms, there are factors in the regulatory environment that mean it is not always so easy to anticipate. Taking a new drug or medical device to market is a long, unpredictable process at the best of times, but clearing that final hurdle of regulatory approval remains a real challenge. 

In this eBook we explore key issues in the current regulatory environment, including the impact of Covid on drug green lights and a potential end-of-year boost to drug approvals.

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