A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
A multi-national European pharmaceutical and consumer health company required clinical data to validate the safety and performance of five of its nasal spray and allergy products post CE-mark, in accordance with MDR 2017/745 Annex XIV Part B.
IQVIA Consumer Health and ObvioHealth designed and conducted all five of these post-market clinical follow-up studies, which were successfully executed in multiple countries across Europe. All study materials were translated into the primary languages spoken in each study’s location.
Digital recruitment for all five studies was designed to target a population that had used the nasal spray products in the past 6 months.
Each study called for participants to complete questionnaires, which were designed to be simple and intuitive to keep compliance rates high. This also allowed for participants to report any adverse events or side effects experienced from using the product.
Recruitment on all these studies was completed below projected budget. The studies reached completion before their targeted end dates, with an average duration of 48 days.
The sponsor was able to gain valuable insights into participant use and satisfaction with the product.
ObvioHealth successfully conducted a clinical trial for RedHill Biopharma to test the safety and efficacy of an oral medication for the treatment of COVID-19 symptoms. We designed this decentralized study to be conducted where the majority of patients recover from illness—in their homes. When the trial was launched in 2021, its unique combination of home health visits, electronic patient-reported outcomes (ePRO), and remote monitoring devices was pioneering—COVID-19 studies were typically conducted inside hospitals.
ObvioHealth and Renovia conducted a groundbreaking study on the efficacy of an at-home medical device for the treatment of stress and mixed urinary incontinence. Read more below to understand how we delivered a successful, fully virtual clinical trial in the midst of the pandemic.