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Supervised In-Use Test under Ophthalmological Control
Supervised in-use test under dermatological control with a 21-day study, 20 volunteers representing all skin types, and final dermatologist sign-off to support safety and marketing claims.
Price per sample:
$4,800
Additional information
| Turnaround Time | 6 weeks |
|---|---|
| Sample Size | enough for 25 panelists |
Supervised In-Use Test under Ophthalmological Control
This study is a 21-day supervised in-use test with 20 volunteers representing a range of skin and eye sensitivities, conducted under the oversight of a qualified ophthalmologist. The study includes clinical assessment and final ophthalmologist sign-off, providing medically supervised data on product tolerance and performance in the eye area.
Products intended for use around the eyes require careful evaluation due to the sensitivity of the area. This study is designed to assess real-world use while maintaining clinical oversight.
Study Purpose
This study evaluates how a product performs when used around the eye area under normal conditions. It focuses on:
- Ocular tolerance
- Skin compatibility in the periocular area
- User comfort and acceptability
It also helps determine whether repeated use may cause irritation, stinging, or discomfort.
Study Design
The study follows a controlled, supervised in-use design over 21 days at a clinical site.
- 20 volunteers representing a range of skin and eye sensitivities
- Product used under normal conditions according to instructions
- Ophthalmologist oversight throughout the study
- Clinical assessment and final sign-off
This ensures results reflect real-world use with appropriate medical supervision.
Study Population
Participants are selected based on the intended product use and sensitivity considerations.
All participants:
- Are in good general health
- Have no active ocular conditions at study start
This ensures that observed effects are attributable to the product.
Evaluation Criteria
Clinical and subjective assessments are performed throughout the study.
Clinical assessments may include:
- Redness
- Watering
- Irritation
- Stinging or burning
- Signs of discomfort
Participants also provide feedback on:
- Comfort during use
- Sensory experience
- Overall acceptability
Both clinical observations and user feedback contribute to the final evaluation.
Claims Supported
This study can support a range of marketing and safety claims, including:
- Ophthalmologist tested
- Ophthalmologically tested
- Clinically tested
- Tested under ophthalmological control
- Suitable for use around the eyes
- Gentle on eyes (subject to results)
- Non-irritating to eyes (subject to results)
Final claim support depends on study outcomes and regulatory considerations.
Data Review and Reporting
At the conclusion of the study:
- Data is summarized using descriptive analysis
- A clear and structured report is issued
- A final evaluation and sign-off by the ophthalmologist is included
The report is suitable for use in safety documentation, regulatory submissions, and marketing support.
Why Choose Pentyl Labs
Pentyl Labs coordinates supervised in-use testing with:
- Clear study protocols
- Reliable timelines
- Easy-to-interpret reports
- Integration with broader testing programs
We also support related services such as dermatological testing, HRIPT, safety assessments, and claims substantiation.
Get Started
Contact [email protected] to request a Supervised In-Use Test under Ophthalmological Control.
Description
Supervised In-Use Test under Ophthalmological Control
This study is a 21-day supervised in-use test with 20 volunteers representing a range of skin and eye sensitivities, conducted under the oversight of a qualified ophthalmologist. The study includes clinical assessment and final ophthalmologist sign-off, providing medically supervised data on product tolerance and performance in the eye area.
Products intended for use around the eyes require careful evaluation due to the sensitivity of the area. This study is designed to assess real-world use while maintaining clinical oversight.
Study Purpose
This study evaluates how a product performs when used around the eye area under normal conditions. It focuses on:
- Ocular tolerance
- Skin compatibility in the periocular area
- User comfort and acceptability
It also helps determine whether repeated use may cause irritation, stinging, or discomfort.
Study Design
The study follows a controlled, supervised in-use design over 21 days at a clinical site.
- 20 volunteers representing a range of skin and eye sensitivities
- Product used under normal conditions according to instructions
- Ophthalmologist oversight throughout the study
- Clinical assessment and final sign-off
This ensures results reflect real-world use with appropriate medical supervision.
Study Population
Participants are selected based on the intended product use and sensitivity considerations.
All participants:
- Are in good general health
- Have no active ocular conditions at study start
This ensures that observed effects are attributable to the product.
Evaluation Criteria
Clinical and subjective assessments are performed throughout the study.
Clinical assessments may include:
- Redness
- Watering
- Irritation
- Stinging or burning
- Signs of discomfort
Participants also provide feedback on:
- Comfort during use
- Sensory experience
- Overall acceptability
Both clinical observations and user feedback contribute to the final evaluation.
Claims Supported
This study can support a range of marketing and safety claims, including:
- Ophthalmologist tested
- Ophthalmologically tested
- Clinically tested
- Tested under ophthalmological control
- Suitable for use around the eyes
- Gentle on eyes (subject to results)
- Non-irritating to eyes (subject to results)
Final claim support depends on study outcomes and regulatory considerations.
Data Review and Reporting
At the conclusion of the study:
- Data is summarized using descriptive analysis
- A clear and structured report is issued
- A final evaluation and sign-off by the ophthalmologist is included
The report is suitable for use in safety documentation, regulatory submissions, and marketing support.
Why Choose Pentyl Labs
Pentyl Labs coordinates supervised in-use testing with:
- Clear study protocols
- Reliable timelines
- Easy-to-interpret reports
- Integration with broader testing programs
We also support related services such as dermatological testing, HRIPT, safety assessments, and claims substantiation.
Get Started
Contact [email protected] to request a Supervised In-Use Test under Ophthalmological Control.
