Cosmetics · Nutraceuticals · Ayurveda · Personal Care

Clinical Research and Claims Studies India: Cosmetics, Nutraceuticals, and Ayurveda

Claim with Confidence.

Human studies for product claims, with no CDSCO drug approval required. Ethics Committee approved, dermatologist supervised, and accepted by the CDSCO Cosmetics Division, FSSAI, EU regulators, and major Indian and international retail buyers.

What is this?

Human clinical studies that substantiate product claims for non-drug categories. No CDSCO drug approval required.

Who is it for?

Cosmetics, personal care, nutraceutical, herbal, and Ayurvedic brands building safety, efficacy, and performance claims.

Why Auriga?

105+ studies. 530+ products tested. 8 claim-specific instruments in-house. Dermatologists on-site.

Request a Study Proposal Call +91-7428116100

Why Auriga

Auriga has been running cosmetic and nutraceutical claims studies since before most D2C brands existed. 105+ safety studies. 530+ products tested. Instruments in-house including Corneometer, Mexameter, Cutometer, Tewameter, and four others. Certified dermatologists on-site. Studies conducted under Independent Ethics Committee approval and accepted by the CDSCO Cosmetics Division, FSSAI, and major retail buyers.

105+

Safety studies completed

530+

Products tested

8

In-house claim instruments

EC Approved

Independent Ethics Committee oversight

Three Study Verticals

Cosmetics and personal care, nutraceuticals, and Ayurvedic and herbal studies. Each vertical has its own regulatory framework and claim categories.

Dermatologist supervised cosmetic clinical study

Cosmetics & Personal Care Studies

Safety and efficacy claim substantiation for skincare, sunscreens, haircare, body care, and personal care products. HRIPT, BIS 4011 patch testing, SPF claim substantiation, and instrument-based efficacy studies.

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Nutraceutical clinical study sample collection

Nutraceutical Studies

Bioavailability, efficacy, and safety studies for food supplements and nutraceuticals. Pathway support for FSSAI nutritional claims and Disease Risk Reduction claims under CDSCO.

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Ayurvedic clinical study consultation

Ayurveda & Herbal Studies

AYUSH-aligned clinical research for classical and proprietary Ayurvedic formulations, and Marketed Ayurvedic Product studies for established herbal brands.

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Which Track Does Your Product Need?

The regulatory pathway depends on your product category and the type of claim. We will confirm the correct track during the initial consultation.

Cosmetics & Personal Care

Pathway
Ethics Committee approval. No CDSCO drug approval required.
Example Claims
Dermatologically tested · Non-irritant · Clinically proven · Moisturising · Anti-ageing · Sensitive-skin tested · 12-hour and 24-hour wear claims.
Open vertical

Nutraceutical — Nutritional / Efficacy Claim

Pathway
FSSAI substantiation pathway. Ethics Committee approval. No CDSCO drug application required.
Example Claims
Supports immune function · Improves bioavailability · Supports muscle strength · Supports bone health.
Open vertical

Nutraceutical — Disease Risk Reduction Claim

Pathway
CDSCO clinical trial pathway. NDCT Rules 2019.
Example Claims
Reduces risk of Type 2 diabetes · Lowers cholesterol · Prevents osteoporosis.
Open vertical

Ayurvedic & Herbal Products

Pathway
Ethics Committee approval. AYUSH-aligned protocols. No CDSCO drug approval required for marketed Ayurvedic products.
Example Claims
Marketed Ayurvedic Product studies · Classical and proprietary formulation studies · Safety and tolerance support.
Open vertical

Eight In-House Claim Instruments

Each claim is supported by a specific instrument and protocol, so the resulting data maps directly to the statement on your packaging.

Corneometer

Moisturisation and hydration claims.

Mexameter

Skin lightening and radiance claims.

Cutometer

Anti-ageing and skin firmness claims.

Tewameter

Skin barrier and antiperspirant claims.

Sebumeter

Anti-acne and pore-refining claims.

pH Meter

pH-balanced and scalp health claims.

BTBP Clarity 2D and 3D

Wrinkle, texture, and pigmentation imaging.

DermLite DL5

Hair and scalp imaging.

Who Engages Auriga for Claims Studies

Six buyer profiles use the Clinical Research and Claims Studies division.

D2C Beauty & Personal Care Founders

D2C founders launching skincare, haircare, body care, and personal care brands who need "dermatologically tested" and other on-pack claims supported by clinical data.

Cosmetics Brand Owners

Established cosmetics brands building or refreshing efficacy and safety claims across skincare, sunscreen, and personal care portfolios.

Nutraceutical & Wellness Brands

Nutraceutical and functional supplement brands needing bioavailability, efficacy, or claim substantiation evidence aligned with FSSAI requirements.

AYUSH Supplement Companies

Herbal and Ayurvedic supplement brands developing studies for AYUSH product registration, label claims, and retailer due diligence.

Marketed Ayurvedic Product Brands

Established Ayurvedic brands running Marketed Ayurvedic Product studies to support efficacy and safety claims for commercial products.

Brands Needing Retail Buyer Evidence

Brands selling through modern retail, pharmacy chains, marketplaces, and beauty retail that require clinical evidence as part of buyer due diligence.

Claims Studies vs Regulated Clinical Trials

Auriga runs both. Most brands engaging this hub are looking for claim substantiation. Drug and Disease Risk Reduction studies use a different pathway.

Claims Studies (this hub)

Cosmetics, personal care, nutraceutical, herbal, and Ayurvedic product studies under Ethics Committee approval. No CDSCO drug approval required.

Regulated Clinical Trials

Phase II to Phase IV clinical trials for new drug approvals and post-marketing studies. Requires CDSCO Clinical Trial Application, CTRI registration, and ICH-GCP execution.

Open Phase II–IV Trials

Related Services

Cosmetics & Personal Care Studies HRIPT · BIS 4011 · SPF · instrument efficacy Nutraceutical Studies Bioavailability · efficacy · FSSAI and CDSCO tracks Ayurveda & Herbal Studies Marketed Ayurvedic Product studies CRO Hub Full CRO capabilities overview Phase II–IV Clinical Trials CDSCO regulated track Personal Care Manufacturing CDMO private label manufacturing

Frequently Asked Questions

Do these studies need CDSCO drug approval?
No, in most cases. Cosmetic, personal care, herbal, and most nutraceutical claim substantiation studies are conducted under Independent Ethics Committee approval following ICMR ethical guidelines. No CDSCO drug clinical trial application is required for marketed cosmetics, marketed Ayurvedic products, or nutritional and efficacy claims. CDSCO clinical trial approval is required only when a nutraceutical product makes a Disease Risk Reduction claim, which places it at the food and drug boundary.
What studies does Auriga run under this division?
Cosmetic safety and efficacy studies including HRIPT, BIS 4011 patch testing, and SPF claim substantiation. Nutraceutical bioavailability and efficacy studies. Ayurvedic Marketed Product studies and classical formulation studies. Instrument-based efficacy studies using Corneometer, Mexameter, Cutometer, Tewameter, Sebumeter, pH Meter, BTBP Clarity 2D and 3D, and DermLite DL5.
How much study experience does Auriga have?
Auriga has completed 105+ safety studies and 530+ products tested across cosmetics, personal care, nutraceuticals, and Ayurvedic categories. The team has been running claim substantiation studies for the Indian cosmetics and supplement industry since before the current D2C wave.
Are the studies dermatologist supervised?
Yes. Cosmetic and personal care studies are conducted under dermatologist supervision with Independent Ethics Committee approval. Where studies require dermatological grading, instrumental measurement, or photographic documentation, certified dermatologists are involved through the study.
Will my study data be accepted by retailers and regulators?
Data generated through this division is accepted by the CDSCO Cosmetics Division, FSSAI for nutraceutical claims aligned to FSSAI Nutraceutical Regulations, EU regulators (Cosmetic Regulation 1223/2009 for cosmetics), and major Indian and international retail buyers for on-pack claim substantiation.
How is this different from Auriga's regulated clinical trials?
Regulated Phase II to Phase IV clinical trials require CDSCO Clinical Trial Application, CTRI registration, and ICH-GCP execution for new drug approvals and post-marketing studies. The Clinical Research and Claims Studies division covers non-drug, claim-substantiation studies for cosmetics, nutraceuticals, and Ayurvedic categories, conducted under Ethics Committee approval. Both divisions operate alongside one another at Auriga.

Request a Study Proposal

Cosmetics, nutraceutical, and Ayurvedic claim substantiation studies. Ethics Committee approved, dermatologist supervised, with 105+ studies and 530+ products on record.

+91-7428116100 Request a Study Proposal

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