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#1

EFPIA W.A.I.T. | Blog

The European Federation of Pharmaceutical Industries and Association (EFPIA) Waiting to Access Innovative Therapies (W.A.I.T.)

#2

The U.S. | Blog

Democrats have revealed that the next major legislative package—colloquially known as the infrastructure package—will likely include provisions to lower prescription drug prices.

#3

Biden Supports Waiving IP Protections for COVID-19 Vaccines. | Blog

As you may have read, the Biden administration announced last week that it will support a proposal to temporarily waive certain intellectual property (IP) protections for COVID-19 vaccines and therapies.

#4

Multiple inflection points are colliding that will force action on drug pricing in the U.S. | Blog

An update on the latest developments in Washington critical to Pharma leaders.

#5

Post–Biogen’s Aduhelm Approval, Prepare for Increased Scrutiny | Blog

Within a few days of the Aduhelm approval, the conversation quickly shifted from the first treatment for Alzheimer’s disease to the exorbitant cost ($56,000 annually) and whether the budgetary impact on society of the drug’s broad label is worth the therapeutic outcomes.

#6

POV: Shifting winds - policy changes threaten decades of progress in orphan medicines | Blog

The World Orphan Drug Congress Europe (WODC) looked back on the remarkable achievements of the last 20 years of the General Pharmaceutical Legislation (GPL) in Europe.

#7

Biden Executive Order Makes Communicating Your Value Proposition More Important than Ever | Blog

This month, we’ve seen a flurry of activity that confirms Washington will be focused on drug pricing this summer, and it’s coming from all directions: Congress, the Biden Administration, and Courts.

#8

A New Drug Price Deal Signals Significant Policy Shift | Blog

This month policies aimed at lowering drug prices are back on the table.

#9

What Biogen’s Alzheimer’s Drug Approval Means for Life Sciences Companies | Blog

In a highly anticipated decision, the Food and Drug Administration (FDA) last week cleared Alzheimer’s disease drug aducanumab on an accelerated, conditional approval program.