New PwC Report- Regulatory Innovation Should Adapt to New Health Economy


Applied Clinical Trials

Forty-three percent of pharma and life sciences execs now support FDA evaluating drugs based on both clinical and economic effectiveness

NEW YORK, Jan. 26, 2015 – Consumers and drug and device manufacturers are changing practices and shifting attitudes toward the Food and Drug Administration (FDA).  Increased pressures for speedy access to breakthrough drugs and medical devices, and a focus on value in addition to medical benefit, are driving these changes. Those changes will likely put pressure on the FDA to consider changes as well. So concludes “The FDA and industry: A recipe for collaborating in the New Health Economy,” a new report from PwC’s Health Research Institute (HRI) based on findings from surveys of consumers and senior industry leaders.

“To meet 21st century demands for innovation, it will be important for drug and medical device manufacturers to collaborate with the FDA to consider changes to the regulatory framework,” said Mike Swanick, global pharmaceuticals and life sciences leader. “While recognizing the FDA’s investments to improve its relationships with manufacturers and speed drug and device delivery, manufacturers still want greater flexibility in product development and review.”

The report reveals how drug and device companies are adapting to the New Health Economy, including consumer and insurer focus on cost-effectiveness as well as medical benefit.  Forty three percent of survey respondents said they are willing to have their products judged based on both clinical and economic value, compared to just 14 percent in 2010.

Additional key findings of The FDA and industry include:

·         Seventy-eight percent of executives said that the FDA has improved the quality and frequency of its communications in the past two years. 

·         Seventy-six percent think that the agency provides actionable feedback and 70 percent think it offered more applicable guidance, rules and regulations in the past two years.

·         Seventy-one percent believe that the FDA can accelerate approval programs by balancing swifter approval with increased post-market surveillance.

As to healthcare consumers, the survey found that they want input into developing therapies.  Relatively few (39 percent) believe the FDA incorporates their views in the agency’s review process, and only 38 percent say that drug and device manufacturers adequately consider their views. 

“With greater access to medical information than ever before, consumers are assuming responsibilities that have historically resided with the FDA or industry – such as developing guidance, creating incentive programs, and funding research and development directly,” said Michael Mentesana, PwC's U.S. pharmaceutical and life sciences research and development advisory services leader. “As a result, companies have a real opportunity to seek out and use consumer feedback to better demonstrate value over existing therapies.”




Related Videos
Related Content
© 2024 MJH Life Sciences

All rights reserved.