header image
Meet the myriad agency requirements in study design, approval and fielding, yet generate meaningful data in a timely and efficient manner

Leverage a world class consulting firm’s experience, utilizing their network of excellent investigators & analysts.
Qualititative and quantitative research studies which meet and exceed client requirements.
For years CharlesGroup has conducted research studies for various teams at Nektar. IRB controlled quantitative device evaluation studies. HFE studies. Qualitative studies with patient subjects. Some of our investigators have product design and development objectives; others have clinical implication objectives. Our professionals listen to patients and customers with a different set of ears. They produce insights and synthesize information in a way most investigators do not.

Given the multitude of constraints and requirements with which studies must comply, it’s often a challenge to meet the most fundamental objective: ensure that human insight rises to the top of the collection of findings so that it can inform product development.

Our understanding of our clients’ technology, the therapeutic area in which they want to introduce it, and the agency requirements for study design, approval and fielding, enables us tp design thorough, efficient programs which produce the data and the outcomes Nektar requires.

Our reporting keeps the consumer at the front and center of all findings, so that product engineers can see all available opportunities to make the technology produce an optimal patient experience.