RELIABLE & HIGH-QUALITY
LABORATORY SERVICES

PHYSICOCHEMICAL

Physicochemical Characterization

Assessment of physical and chemical properties

Residue and Trace Analysis Studies

Detection of residues and trace compounds

Toxicity Studies (In vivo & In vitro)

Safety evaluation using in vivo and in vitro models

Biocompatibility and Biological

Biological evaluation of medical devices

Microbiological Studies

Microbial analysis and testing

Genotoxicity and Mutation Studies

Genetic damage and mutation assessment

Pharmacokinetics Studies

Role of Pharmacokinetics in Product Development

Pharmacodynamic Studies

Biological effect and efficacy assessment

NANOTOX–PART OF THE NANOLAB GROUP

NanoTox is a specialized GLP-focused laboratory within the Nanolab Group, with core expertise in toxicology, safety assessment, and regulatory studies.

In addition to Toxicology, NanoTox maintains strong scientific and operational capabilities across multiple GLP laboratory disciplines, delivering reliable, internationally aligned testing solutions supported by advanced analytical infrastructure and expert teams.

⁺ 5000

BUSINESS PARTNER

5000 ^m2

FACILITY

⁺ 200

EMPLOYEES

6

LABORATORIES

⁺ 15

YEARS OF EXPERIENCE

⁺ 33

PRODUCT ANALYSIS

⁺ 25

INDEPENDING TESTING

⁺ 1000

TESTING METHODS

WE'R TRUSTED EXPERTS
GLP LABS

Test Product Groups – Regulatory & Safety Assessment Portfolio

We provide comprehensive testing and regulatory evaluation services across a wide range of product groups to ensure safety, quality, and compliance with international standards.

Test Product
Groups

EXPLORE OUR TEST UNITS.

We provide GLP-compliant, multidisciplinary preclinical testing services supporting reliable biological safety evaluation under OECD, ICH and ISO standards.

In Vivo Test Unit

GLP-compliant in vitro cell culture testing for biological safety and biocompatibility assessment under OECD and ISO 10993 standards.

Cytotoxicity testing (MTT, NRU, XTT)
Skin irritation and corrosion testing (RhE, OECD TG 430/431)
Eye irritation testing (BCOP, ICE, RhCE)
Skin sensitisation testing (DPRA, KeratinoSens™, h-CLAT)

Pathology Test Unit

GLP compliant pathology and histopathology services for toxicology and biocompatibility assessment under OECD GLP standards.

Necropsy and organ weight analysis
Histotechnology and tissue processing
Histopathology evaluation
Clinical pathology testing
Tissue reaction grading

Physico-Chemical Test Unit

GLP compliant analytical testing for identity, purity, potency and impurity profiling under ICH and ISO 10993 frameworks.

Active ingredient assay
Impurity profiling (HPLC / GC-MS / LC-MS)
Physical characterisation (pH / viscosity / particle size)
Extractables & leachables studies
Method validation (ICH Q2)

Genetic Toxicology Unit

GLP compliant genotoxicity testing for regulatory safety assessment of pharmaceuticals, chemicals and medical device extracts under OECD and ICH guidelines.

Ames bacterial reverse mutation test
In vitro micronucleus test
Chromosomal aberration test
Gene mutation assays (HPRT / MLA)
In vivo micronucleus test

Microbiology Unit

GLP and GMP compliant microbiological testing of pharmaceuticals, medical devices and cosmetics for sterility, bioburden and contamination control.

Bioburden testing
Sterility testing
Endotoxin testing (LAL / rFC)
Specified organism detection
Antimicrobial effectiveness testing

In Vitro Cell Culture Unit

GLP and ISO 10993 compliant in vitro biological evaluation for cytotoxicity, irritation and sensitisation testing using validated mammalian cell systems.

Cytotoxicity testing (MTT / NRU / XTT)
Skin irritation (RhE models)
Skin corrosion testing
Eye irritation assays
Skin sensitisation assays

WE OFFER SEAMLESS AND SUSTAINABLE SOLUTIONS PARTNERSHIPS ACROSS CONTINENTS

A global standard in analytical excellence, combining science, quality, and compliance to deliver results you can rely on worldwide.

⭐️⭐️⭐️⭐️⭐️- Scope

⭐️⭐️⭐️⭐️⭐️- Price

⭐️⭐️⭐️⭐️⭐️- Customer Satisfaction

⭐️⭐️⭐️⭐️⭐️- Impact Communication

UNITED BY SCIENCE, CONNECTED THROUGH INNOVATION WORLDWIDE LABORATORY PARTNERSHIPS

OUR ADVANTAGE

We demonstrate OECD GLP compliance with accreditation certificates and offer uninterrupted solutions with testing services authorized by the necessary legal authorities.

Accredited Lab

Comprehensive Scope

OECD Compliance

Quality Assured

Active Data Integrity

Globally Compliant FDA & EA Reporting

ACCREDITATIONS & COMPLIANCE

High Quality Lab Services

We are all the team experts and specialists of particular branches falls into
researches and diagnosis, ready to serve you at their best.

Request

Easy Accessibility

Customers can easily reach us and submit their requests through multiple channels, including e-mail, telephone, live support, face-to-face communication, and social media.

Feasibility & Quotation

Scientific & Regulatory Scoping

Each enquiry is reviewed by our scientific team to confirm test-item suitability, applicable regulatory framework (OECD, ICH, ISO, FDA, EMA), and study feasibility. A detailed technical and commercial proposal is then issued.

Order

Contract & Sponsor Agreement

We offer cost-effective solutions with competitive pricing, supported by our wide service scope and solution-oriented approach.

Study Plan & Protocol Approval

GXP-Compliant Study Design

A study-specific protocol is prepared by the Study Director, reviewed by the QAU, and approved by the Sponsor before initiation, in accordance with OECD GLP and 21 CFR Part 58.120 / 58.130 and GXP guidelines.

Services

Conduct of the Study

In addition to analysis methods validated according to national and international methods, we provide quality service with TS EN ISO/IEC 17025 standard accreditation and OECD GLP and 21 CFR Part 58.120 / 58.130 and GXP guidelines.

Quality Assurance & Audit

Independent QAU Oversight

Every GXP study is independently monitored by our Quality Assurance Unit through facility-, process- and study-based audits, ensuring data integrity (ALCOA+) and full compliance with OECD GLP, ISO/IEC 17025 and 21 CFR Part 58 and GXP guidance.

Final Report & Archiving

Regulator-Ready Deliverable

A signed Final Report including the Study Director's GLP Compliance Statement and QAU Statement is issued to the Sponsor. All raw data, specimens and records are securely archived in line with OECD GLP and 21 CFR §58.190 retention requirements.

Support After Sale / Measuring Customer Satisfaction

Effective communication/Evaluation

We have customer representatives who deal with our customers' requests and questions after the service. Customer satisfaction data is evaluated statistically with the help of a post-service survey.