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PhRMA president and CEO Stephen J. Ubl joined Fox Business’ Maria Bartiromo on “Mornings with Maria” today to discuss bold steps the biopharmaceutical industry has taken in the last few months as part of its commitment to advance a multifaceted solution to address the opioid crisis. Most recently, PhRMA announced its support for policies limiting the supply of opioids to seven days for acute pain treatment.

PhRMA has also been working closely with the President’s Commission on Combating Drug Addiction and the Opioid Crisis, the National Institutes of Health (NIH) and the Food and Drug Administration to develop a public-private partnership that will accelerate the development of non-opioid, non-addictive pain medicines and medication-assisted treatments for long-term addiction recovery. The public-private partnership would allow increased information sharing and collaboration between government and industry to speed the drug development process.

Holly Campbell

Holly Campbell is former deputy vice president of public affairs at PhRMA focusing on the cost and value of medicines.

Holly Campbell

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New analysis: Accelerated approval pathway is changing lives in underserved communities

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Florida’s importation plan puts patients in danger

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The Biopharmaceutical Industry Still Needs Clarity from the FDA on Orange Book Listings

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Decentralized clinical trials and the future of drug development

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Navigating the Patient Experience Survey: Protecting Lifelines to Access and Innovation

July 26, 2023

How FDA’s modernization strategy could improve drug development

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Setting the record straight on accelerated approval

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FDA should remain the authority on the safety and effectiveness of medicines

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Recognizing National Glaucoma Awareness Month

February 1, 2023

What you should know about real-world evidence and drug development

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In their own words: Insured Americans support policy reforms that address access and affordability concerns

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Three things to know about the accelerated approval pathway

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PDUFA and BsUFA reauthorizations are wins for patients

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Navigating the patient experience: Burdens and barriers standing between patients and their care

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This week’s reading list: All the reasons the Senate-passed drug pricing bill is bad policy

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Myth vs. Fact: The Senate’s latest price setting proposal

August 5, 2022

ICYMI: Patients across the country are sharing concerns about government price setting

August 3, 2022

New analysis finds deeper impact of drug pricing bill on biopharmaceutical researchers

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ICYMI: A patient, physician, biotech investor and industry leaders warn about the dangers of government price setting bill

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The Patient Perspective: Government price-setting harms patients

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Word of the Month: Biomarkers and surrogate endpoints

July 11, 2022

Why drug importation is bad for Americans

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Ensuring timely reauthorization of PDUFA and BsUFA

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Spotlighting a growing mental health challenge

May 9, 2022

The accelerated approval pathway: Helping patients with serious or life-threatening diseases

March 17, 2022

The importance of timely PDUFA and BsUFA reauthorization

February 3, 2022

ICYMI: New approvals by the FDA in 2021 offer greater treatment options for patients

January 26, 2022

Insurance design barriers can impact patient adherence and can lead to poor health outcomes

November 23, 2021

Biosimilar User Fee Act (III) Performance Goals Letter will help increase options for patients and promote competition

September 28, 2021

Meeting Tomorrow: Looking ahead to PDUFA VII

September 27, 2021

The impact of monoclonal antibodies and COVID-19 recovery

September 2, 2021

PDUFA VII is critical for future biopharmaceutical innovation and for patients

August 23, 2021

How strengthening the biosimilar marketplace benefits patients

May 18, 2021

The FDA Office of Minority Health and Health Equity: Working to advance health equity through diversity in research

May 12, 2021

Getting the 340B program back on track in 2021

March 10, 2021

2020 FDA approvals show innovation despite COVID-19 pandemic challenges

January 26, 2021

Nearly 400 cell and gene therapies in development to target a broad range of diseases

March 10, 2020

PhRMA submits comments on FDA’s proposed rule on drug importation

March 10, 2020

Drug importation: An old idea that is still a bad idea

January 28, 2020

ICYMI: 2019 brings innovative medicines to patients

January 17, 2020

PhRMA comments to Congress on Cures 2.0 call to action

December 18, 2019

Guest Post: Following my stroke, having access to ground-breaking medical innovation has never been more important

September 4, 2019

What they’re saying: Safety is top concern for recent drug importation proposal

August 8, 2019

ICYMI: Canadian government, stakeholders voice concerns with drug importation proposals

August 1, 2019

PhRMA responds to Florida’s request for information on drug importation

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Guest Post: Using the patient voice to go boldly

May 30, 2019

IP Explained: How Hatch-Waxman successfully balances affordability and innovation

May 22, 2019

PhRMA CEO raises concerns with Florida importation proposal, highlights reforms needed to lower costs for patients

May 8, 2019

Guest post: Hearing from patients on Rare Disease Day

February 28, 2019

Rare Disease Day: Unmet medical need inspires biopharmaceutical innovation

February 28, 2019

Look at the facts. Drug importation is dangerous.

February 22, 2019

Why state drug importation pilot programs don’t work

February 8, 2019

PhRMA comments to administration on Medicare Part D proposed rule

January 25, 2019

Putting 2018 medicine approvals in context

January 23, 2019

Keep the Six Protected Classes, protected

January 22, 2019

FDA needs best and brightest to advance a new era of medicine with America’s biopharmaceutical companies

October 16, 2018

Balancing innovation and competition in the biologics marketplace

October 11, 2018

What if a couple of small fixes could protect seniors in the donut hole and save them money on out-of-pocket costs?

September 13, 2018

How much do you know about Medicare Part B?

July 31, 2018

How ICER’s assessment of a new class of migraine treatments fails patients

July 10, 2018

New analysis shows that more medicines worldwide are available to U.S. patients

June 5, 2018

New 340B analysis: Hospitals raking in billions while uncompensated care drops by billions

May 15, 2018

Securely dispose of your unwanted medicines on National Take Back Day

April 28, 2018

Spending on medicines grew less than one percent in 2017

April 19, 2018

New report shows over 500 medicines in development for neurological disorders

April 18, 2018

Rare Disease Day: Unmet need inspires innovation

February 28, 2018

Innovation comes in many forms, including new and expanded uses of existing medicines

January 29, 2018

Fact Check Friday: The truth about the cost of 340B to patients

January 26, 2018

340B Spotlight: New pieces of legislation continue momentum to fix 340B program

January 18, 2018

ICYMI: Why 2017 medicine approvals matter

January 12, 2018

New surveys find payers and providers want more data from biopharmaceutical companies

December 6, 2017

Supporting opportunities for enhanced competition in the marketplace

November 22, 2017

340B Spotlight: ICYMI – 340B hearing, new reports highlight growing need for program reform

October 20, 2017

The Washington Post retracts PhRMA claim in opioid story

October 18, 2017

PhRMA response to Washington Post and 60 Minutes stories

October 16, 2017

Protect your health: Important disaster preparedness tips for Harvey and Irma

September 6, 2017

PhRMA Supports President’s Commission’s Holistic Approach on Opioid Crisis

August 2, 2017

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July 27, 2017

Why reauthorization of PDUFA matters

July 13, 2017

A critical opportunity to prevent prescription drug abuse

June 2, 2017

Former law enforcement officials raise concerns with drug importation proposals

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Resources for understanding the dangers of drug importation

March 28, 2017

Medicare Monday: A discussion on affordability and access to medicines

March 27, 2017

17 years (and more) of medical discoveries

March 24, 2017

Guest Post: The importance of a modern FDA in drug discovery

March 22, 2017

How drug importation schemes could increase U.S. law enforcement burdens

March 16, 2017

Case Study: How one online pharmacy knowingly endangered U.S. consumers

March 2, 2017

Why drug importation threatens patient safety

February 28, 2017

Fact Check Friday: The truth about drug importation and patient safety

February 24, 2017

How do multiple sclerosis patients define value?

February 24, 2017

ICYMI: New era of medicine initiative kicks off in Boston

February 22, 2017

What you don’t know about importation from Canada

February 17, 2017

Biopharmaceutical industry’s success reducing disparities for African Americans

February 16, 2017

Discovery of counterfeit hepatitis C drug is another example of why importation is bad for patients

February 13, 2017

VIDEO: PhRMA CEO discusses industry response to opioid crisis on Mornings with Maria

FDA

Patients

Prescription Drug Safety

VIDEO: PhRMA CEO discusses industry response to opioid crisis on Mornings with Maria

October 12, 2017

VIDEO: PhRMA CEO discusses industry response to opioid crisis on Mornings with Maria

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