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Advanced Science Laboratories Incorporated

Clinical Testing Facility

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      • SPF Testing
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Guidelines and Terms

Procedures:
Whenever possible, tests are performed by approved official methods derived
from regulatory and government procedures and monographs as well as published
methodology.

Custom Analyses can be performed and new methods developed to satisfy specific
testing needs on request. We can develop unique, custom tailored protocols to
accommodate almost any test requirements, utilizing specialized panelist bases
including but not limited to age, skin conditions, ethnicity, and gender.

 

Test Results:
A signed and dated Final Report describing all results together with photography,
PhotoGrammetrix™ in digital or print media, if applicable, is submitted upon completion
of testing. Raw data is always available on site or in duplicate for your records. Special
arrangements can be made to receive interim results if necessary. Our unique Graphic
Arts Department can assist with imaging from miniature, website and brochures to
poster and billboard files. Images suited for commercial reproduction taken directly from
scientific studies conserve marketing costs.

 

Confidentiality:
Client confidentiality is a top priority at Advanced Science Laboratories. The company is always willing to sign specialized mutual NDA’s (Non–Disclosure Agreements) and targeted confidentiality
agreements.

 

Sample Submission:
The Advanced Science Laboratories Sample Submission Form must accompany all samples. Perishable products should be packed in dry ice and shipped during the early part of the week.

If necessary, ADVANCED will advise you on the quantity of material needed to meet specific testing requirements. Generally, a minimum of 120 grams is required.
Repeat Insult Patch Testing (RIPT) and Photoallergy Studies require 400-gram samples.
Please note that sample submission forms can be downloaded directly from the
Advanced website and sent in with your product:

 

Sample Submission Form Page

 

Sample Preparation:
Because the matrix of many products varies considerably, special sample preparation
and compositing may be required. In such instances, the fee is approximately $25 –
$75 per sample, per day. An additional charge will be assessed to samples requiring
excessive extraction, heating, formulating or other procedures.

 

Prerequisite Safety Data:
All samples submitted for presentation to human skin must have completed safety
assessments prior to study commencement. Studies must include:

• USP or PCPC (formerly CTFA) Preservative Efficacy Test (PET) – preferably 56 day
double challenge – anhydrous samples excluded
• In-vivo Skin Irritation Tests (example: RIPT, Comedogenicity, Phototoxicity, etc.)
• In-vitro Eye Irritation Tests, if applicable (example: ‘no tears claims’, ophthalmologist/
optometrist tested studies, etc.)
• 90 Day Accelerated Stability and Container Compatibility Study

Responsibility for conducting the above studies belongs to the Sponsor. In the event
requested tests are not received in a timely fashion prior to study commencement our
assurance of compliance with these requirements will be covered by a section in the
Final Report indicating:

“Sponsor purports the following tests have been conducted with no adverse events
and that the test data are on file on their premises and have not been made available to
ADVANCED personnel followed by a listing of the applicable test titles.”

 

Sample Retention Policy:
Unless advised otherwise we retain samples for the following time periods:
• Perishables – 2 months beyond study completion
• Non-perishables – 3 months beyond study completion or up to 3 years if the sample is
known to be in support of a government application
• Return of sample request must be received prior to study commencement

 

Rush Analysis:
ADVANCED will accommodate special emergency situations whenever possible
at the costs listed below. Notification must be communicated in advance.

Rush Fee: 50% of full study cost
Interim Results: $ 2,500 per interim reporting

 

Archiving:
All original samples, raw data sheets, technician’s notebooks, correspondence files,
copies of final reports and remaining specimens are maintained on the premises of
Advance Science Laboratories Inc. in limited access marked storage files for a period
not to exceed two years. A duplicate digital copy of final reports is separately archived in a bank safe deposit vault. Sponsors are encouraged to keep all original, signed, dated and
certified reports. ADVANCED will not be responsible, and it will not be possible to provide
duplicate original hard copies of reports once the documents leave our premises.

 

Terms:
Net on presentation. 2.0% monthly service charge on past due balances.

 

Discounts:
Discounts are available based on project volume.

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  • SPF Testing In-Vivo Measurements
  • SPF Testing In-Vitro Measurements
  • Product Efficacy Studies
  • RIPT for Hypoallergenic Claims
  • Blue Light and Infrared Protection
  • Moisturization & Skin Hydration
  • Antiperspirant Efficacy
  • Matched Scientific Photography, MSP™
  • PhotoGrammetrix Analysis, PhGx®
  • PolyChrommetrix 3D Modeling, PcMx®
  • Instrumental Claim Support
  • Hair & Nail Studies
  • Color Persistence Evaluations

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Blue Light Testing!

Blue Light, also known as High Energy Visible Light (380-530nm), testing method designates protection capabilities via in-house generated High Energy Visible Light Protection Factor (HEV-PF) calculated from spectrometric measurements performed over the 380-530nm spectral range.

Visible Light (400-700nm) testing method designates protection capabilities via in-house generated Visible Light Protection Factor (VIS-PF) calculated from spectrometric measurements performed over the 400-700nm spectral range.

 

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216 Congers Road | Building 1 | New City, New York 10956, USA
+1 845.634.1500 p | +1 845.634.5565 f
This site last updated April 24, 2025

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