blog

The Patient Experience Company

By BBK Worldwide on Mon, Jun 25, 2018 | 3 min read

Over the past 35 years, BBK Worldwide has driven the development of patient recruitment and engagement through our products, services, experience, and thought leadership. With this in mind, we are pleased to announce our new marketplace position as The Patient Experience Company.

Topics: DIA 2018, Patient Experience

At DIA 2018, We’re All About Experience – the Patient’s & Yours

By Aaron Fleishman on Wed, Jun 20, 2018 | 2 min read

 

 

For those of us in the clinical R&D industry, this is among the most exciting (and busiest) times of the year. I’m talking, of course, about the Drug Information Association (DIA) Annual Meeting, June 24-28 in Boston.

With industry stakeholders gathering in our own backyard to exchange ideas in the pursuit of developing new therapies and accelerating efforts to enhance health and well-being, we could not be more thrilled. Ask anyone who has attended the DIA in the past, and they will tell you that it’s an occasion where a lot of exciting work gets done in a very short period of time.

Every year that we attend the DIA, we do our best to honor the spirit of the occasion and to acknowledge the importance of our industry colleagues working together in such a dynamic setting. This year, it is our goal to provide an experience that demonstrates our commitment to the patients who make clinical research possible.

Topics: DIA 2018, Patient Experience

A Caregiver's Perspective on Rare Disease Clinical Trials

By Juli Greenwood on Thu, Apr 27, 2017 | 4 min read

Supporting rare disease research is a big part of our work here at BBK and rare disease recruitment is an expertise that our sponsors and CRO customers have come to expect from us.

While progress has been made to improve the lives of patients with rare disorders, there is much that still needs to be done to reach patients, further research, find new treatments and improve outcomes. Our most recent eBook, “Rare Disease Research. What’s Next?” is a collection of insights from a variety of rare disease stakeholders, including Roberta Carson, Founder and President of Zaggo, Inc. – a national nonprofit devoted to helping patients and families be more engaged members of their medical teams.

Topics: Patient Engagement, Patient Advocacy, Patient Experience

 
Subscribe To Our Blog