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In-Use Test Under Gynecological Control
Gynaecological in-use test to evaluate clinical tolerance and cosmetic acceptability of intimate cosmetic products under normal conditions of use.
Price per sample:
$7,600
Additional information
| Turnaround Time | 6 weeks |
|---|---|
| Sample Size | enough for 25 panelists |
In-Use Test Under Gynaecological Control
Our gynaecological in-use test evaluates how cosmetic products perform when consumers use them on the intimate area under normal conditions. A qualified gynaecologist oversees the study and evaluates tolerance throughout the test period. As a result, the data reflects real product use while maintaining medical oversight.
Because products intended for intimate use require careful safety evaluation, this study helps brands assess comfort, tolerance, and acceptability in a realistic setting. Therefore, many companies use this test to support safety documentation and marketing claims for sensitive-use products.
Study Purpose
This study evaluates how a product affects the intimate area during normal use. Specifically, it examines tolerance, user comfort, and overall acceptability. In addition, the study helps identify whether repeated use may cause irritation or discomfort.
Study Design
The study follows an open in-use design at a single clinical site. Participants receive clear instructions and use the product as directed for a defined period. During the study, clinical staff track progress and collect feedback. After the use period ends, a gynaecologist performs a clinical evaluation.
Because the study mirrors real-world conditions, the results provide practical and relevant insight into product performance.
Study Population
The study includes adult female volunteers selected based on the target product profile. Participants start the study in good health and show no active gynaecological conditions. Therefore, evaluations focus on product-related effects rather than unrelated medical factors.
Evaluation Criteria
Clinicians assess several parameters, including:
-
Redness
-
Swelling
-
Dryness
-
Burning or itching
-
Sensations of discomfort
At the same time, participants complete structured questionnaires to describe their experience. As a result, both clinical observations and user feedback contribute to the final assessment.
Data Review and Reporting
After the study concludes, analysts summarize results using clear descriptive analysis. The final report provides straightforward conclusions on tolerance, comfort, and cosmetic acceptability.
Why Choose Pentyl Labs?
Pentyl Labs coordinates gynaecological in-use testing with clear protocols, practical timelines, and easy-to-read reports. Moreover, we support related services such as HRIPT, safety assessments, and claim support. As a result, study results integrate smoothly into broader product development and compliance programs.
📩 Contact [email protected] to request an In-Use Test Under Gynaecological Control.
Description
In-Use Test Under Gynaecological Control
Our gynaecological in-use test evaluates how cosmetic products perform when consumers use them on the intimate area under normal conditions. A qualified gynaecologist oversees the study and evaluates tolerance throughout the test period. As a result, the data reflects real product use while maintaining medical oversight.
Because products intended for intimate use require careful safety evaluation, this study helps brands assess comfort, tolerance, and acceptability in a realistic setting. Therefore, many companies use this test to support safety documentation and marketing claims for sensitive-use products.
Study Purpose
This study evaluates how a product affects the intimate area during normal use. Specifically, it examines tolerance, user comfort, and overall acceptability. In addition, the study helps identify whether repeated use may cause irritation or discomfort.
Study Design
The study follows an open in-use design at a single clinical site. Participants receive clear instructions and use the product as directed for a defined period. During the study, clinical staff track progress and collect feedback. After the use period ends, a gynaecologist performs a clinical evaluation.
Because the study mirrors real-world conditions, the results provide practical and relevant insight into product performance.
Study Population
The study includes adult female volunteers selected based on the target product profile. Participants start the study in good health and show no active gynaecological conditions. Therefore, evaluations focus on product-related effects rather than unrelated medical factors.
Evaluation Criteria
Clinicians assess several parameters, including:
-
Redness
-
Swelling
-
Dryness
-
Burning or itching
-
Sensations of discomfort
At the same time, participants complete structured questionnaires to describe their experience. As a result, both clinical observations and user feedback contribute to the final assessment.
Data Review and Reporting
After the study concludes, analysts summarize results using clear descriptive analysis. The final report provides straightforward conclusions on tolerance, comfort, and cosmetic acceptability.
Why Choose Pentyl Labs?
Pentyl Labs coordinates gynaecological in-use testing with clear protocols, practical timelines, and easy-to-read reports. Moreover, we support related services such as HRIPT, safety assessments, and claim support. As a result, study results integrate smoothly into broader product development and compliance programs.
📩 Contact [email protected] to request an In-Use Test Under Gynaecological Control.
