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OUR INSIGHTS

How to Coordinate Global Qualitative Interviews in Clinical Trials?
Lasse Schou Rasmussen
Posted by Lasse Schou Rasmussen
October 6, 2021

How to Coordinate Global Qualitative Interviews in Clinical Trials?

Let us be honest. Coordinating any kind of interviews involving several people besides the interviewee themselves is an activity that require close management and daily attention.

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Challenges in obtaining strong feedback from a clinical trial
Jens Harald Kongsø
Posted by Jens Harald Kongsø
August 9, 2021

Five challenges in obtaining strong feedback from clinical trials and ways to overcome them

When pharmaceutical companies have completed a clinical trial, they may want to organise a result meeting with the attendance of participating...

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How to ensure patient safety during clinical trial interviews
Lasse Schou Rasmussen
Posted by Lasse Schou Rasmussen
May 13, 2021

How to ensure patient safety during clinical trial interviews

Despite the many positive aspects of interviewing patients to inform the drug development, there can still be a reluctance within pharmaceutical companies to start collecting direct patient feedback in their clinical trials.

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ISO 9001 certification
Laura Lassen
Posted by Laura Lassen
February 26, 2021

Clinigma® is now ISO 9001 certified

At Clinigma®, we are proud to announce that we have achieved an ISO 9001 certification in designing, conducting, analysing and reporting patient interviews...

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The hassle of interviewing patients in clinical trials without standardised procedures
Laura Lassen
Posted by Laura Lassen
February 15, 2021

The hassle of interviewing patients in clinical trials without standardised procedures

Ensuring that internal procedures are well in place is important for any company as it helps assuring the quality of its products and/or services. In terms of this, pharmaceutical companies...

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Improving the retention of patients in clinical trials
Laura Lassen
Posted by Laura Lassen
January 29, 2021

Improving the retention of patients in clinical trials

Insufficient patient retention in clinical trials is a common issue in the pharmaceutical industry. It has a number of consequences for the drug development...

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