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Biocompatibility & Safety Testing
Chemical Characterization & Risk Assessment
Regulatory & Performance Testing
Biocompatibility Tests:
Systemic Toxicity (ISO 10993-11)
Irritation & Sensitization (ISO 10993-10 & USP)
Implantation Testing (ISO 10993-6 & USP)
Hemocompatibility Testing (ISO 10993-4)
Reproductive & Developmental Toxicity (ISO 10993-3)
Carcinogenicity Testing (ISO 10993-3)
Pyrogenicity Testing
USP Plastics (USP Class IV)
In-Vitro Cytotoxicity Testing (ISO 10993-5)
In-Vitro Genotoxicity Testing (ISO 10993-5)
Sterility
Bioburden Testing
Bacterial Endotoxin Testing
Alternative to Animal Models
Chemical Characterization (ISO 10993-18)
Comprehensive Biological and Toxicological Risk Assessment (ISO 10993-17)
Extractables & Leachables Studies
Impurity / Degradant Toxicity Assessment
Regulatory Documentation & Performance Testing
Biological Evaluation Plans (BEP) & Reports (BER)
Clinical Testing Support
Performance Testing of Devices
Package Testing (ISO 11607 compliance)
Electronic Safety Testing (EMI/EMC)
Risk Assessment & Compliance Support (ISO 14971)
Edit Template
Discovery Chemistry
Discovery Biology
Regulatory Support
In vivo
In vitro
Toxicology
CMC(Chemistry, Manufacturing & Controls) & Formulation
API process development & scale-up
Solid-state & formulation science
Formulation development
Excipients selection & compatibility
Stability & shelf-life studies
Analytics & Bioanalytical Chemistry
Analytics method development & validation(ICH Q2)
Impurity profiling & quantitation
Residual solvents & elemental impurities (ICH Q3C / Q3D)
Dissolution, content uniformity, assay, potency
Batch release testing, CoA, stability-indicating methods
Specialized Routine Testing
Enzyme activity assays (standardized QC panels)
Heparin potency & purity testing
Low Molecular Weight Heparin (LMWH) assays including Enoxaparin
Non-clinical PK studies PK/PD studies & modelling
Efficacy (disease) models Dose-range finding and proof-of-concept studies
Biodistribution & mass-balance (ADME) studies
In vivo DDI/interaction confirmation t
Target validation & target engagement
Cell-based functional assays
In vitro ADME (DMPK)
Permeability & transporter assays
In vitro mechanistic safety screens
Biomarker & PD assay development
Clinical pathology & biomarker panels
GLP bioanalysis / LC-MS/MS capabilities
Biostatistics, data analysis, PK/PD & modelling teams
Drug-drug interaction (DDI) studies
Non-Clinical Safety Testing
In vitro genotoxicity
GLP toxicology studies
Genotoxicity & carcinogenicity
Reproductive & developmental toxicity
Immunotoxicity, hypersensitivity & local tolerance
Histopathology & toxicologic pathology
Impurity toxicology & metabolite safety assessments
Regulatory strategy & agency interaction support
ICH guideline compliance & CTD compilation
Impurity qualification & safety-related assessments
Environmental Risk Assessment (ERA)
Edit Template
In Vivo Animal Studies
Microbiology Testing
Biopharmaceutical Characterization & Functional Assays
Cellular & Molecular Lab Assays
Acute toxicity studies
Sub-acute and sub-chronic toxicity studies
Chronic toxicity studies
Maximum tolerated dose (MTD) determination
Dose range finding (DRF) studies
Pharmacokinetic (PK) and bioavailability studies
Disease and efficacy models
Repeated dose toxicity assessments
Microbiology & Resistance Studies
Sterility testing (per ISO, USP, or pharmacopeial standards)
Bioburden determination and monitoring
Endotoxin testing (Limulus Amebocyte Lysate, LAL)
Antibacterial and antifungal activity assays
Microbial identification / strain typing
Resistance profile screening
Environmental monitoring (surfaces, air, water)
Preservative efficacy (challenge test)
Cell-based & Functional Bioassays (Potency, Immunogenicity, Cytotoxicity)
Mechanism of Action Studies (Receptor Binding, Signal Transduction)
Molecular & Analytical Characterization (HCP, Residual DNA/RNA, Binding Studies)
In Vitro ADME & Stability Studies (Serum/Plasma Stability, Permeability, Protein Degradation)
Stability & Shelf-life Studies (Accelerated, Real-Time, Forced Degradation)
Immunology & Bioanalytical Platforms (Cytokine Release, Immunophenotyping, PK/PD Analysis)
Pathology, Microbiology & Virology Support (Histopathology, Sterility, Mycoplasma, Endotoxin Testing)
Custom Assay Development & Validation
Cytotoxicity Assays (MTT, XTT, LDH, WST-1, Neutral Red)
Cell Proliferation and Apoptosis Studies
Genetic Toxicology Tests (Ames Test, Micronucleus Assay, Chromosome Aberration)
ADME Cellular Models (Caco-2 Permeability, Hepatocyte Metabolism)
Reporter Gene Assays (Mechanism-of-Action)
Flow Cytometry-based Immunophenotyping
Custom Cell-Based Assay Development
Edit Template
Safety & Toxicological Testing
Clinical, Efficacy, and Mechanistic Studies
Purity & Stability Testing
Skin Irritation and Sensitization (OECD 404, LLNA)
Eye Irritation and Corrosion (BCOP, ICE)
Phototoxicity and Photoallergenicity
Acute and Repeated Dose Toxicity
Mutagenicity and Genotoxicity (Ames test, Micronucleus)
Dermal Absorption Studies
Preservative Efficacy Challenge Test
Microbial Limits and Endotoxin Testing
Heavy Metals and Residual Solvent Analysis
Analysis of Restricted and Prohibited Substances
Dermatological Safety: Patch Tests (HRIPT, Cumulative Irritation)
Clinical Efficacy: Moisturization, Anti-aging, Skin Brightening, Anti-acne, Hair Growth
Discovery Biology: Collagen/Elastin Synthesis, Melanin Inhibition, Anti-inflammatory Assays
Microbiome Modulation and Bioassays
In Vitro ADME & Permeation: Skin Absorption, Barrier Function
Custom Assay Development & Claim Validation
Purity, Impurities & Stability Testing (ICH & USP guidelines)
Physical Properties: pH, Viscosity, Spreadability, Particle Size, Zeta Potential
Ingredient Profiling (HPLC, LC-MS, GC-MS, NMR)
Shelf-life and Photostability Testing
Edit Template
Physicochemical Characterization
Biological Efficacy
Toxicology Studies
Regulatory Support
Purity & Impurity Profiling
Physicochemical Property Testing
Solubility, Vapor Pressure, Partition Coefficient, Stability
Spectroscopic & Analytical Method Development (HPLC, GC, MS, NMR)
Viscosity, Particle Size, Zeta Potential
Microbiology & Resistance Studies
Bioactivity & Efficacy Testing (antibacterial, antifungal, insecticidal, herbicidal)
In Vivo Toxicology Studies
Genotoxicity Testing
Ecotoxicity Testing
Impurity / Degradant Toxicity Assessment
Stability & Shelf-Life Studies
Chemical Risk & Exposure Assessment
Custom Assay Development & Validation
Edit Template
Preclinical Efficacy & Mechanistic Studies
Toxicology & Safety Assessment
Regulatory & Compliance Support
In vivo Nutraceutical Efficacy
Glycemic Index & Glycemic Load Estimation
In vitro Nutraceutical Bioactivity
Probiotics
Custom Study Designs
Acute Oral Toxicity Studies
Sub-chronic Toxicity Studies
Genotoxicity Testing
Reproductive & Developmental Toxicity
Skin & Mucosal Irritation Testing
Toxicological Risk Assessment
Novel Food & Dietary Ingredient Submissions
Nutritional Label Validation & Claims Substantiation
Risk Assessment
Edit Template
Contact Us
Request Quote
Home
About
Services
MEDICAL DEVICES
PHARMACEUTICALS
BIOPHARMACEUTICALS
COSMETICS
AGROCHEMICAL
NUTRACEUTICALS
Biocompatibility & Safety Testing
Chemical Characterization & Risk Assessment
Regulatory & Performance Testing
Biocompatibility Tests:
Systemic Toxicity (ISO 10993-11)
Irritation & Sensitization (ISO 10993-10 & USP)
Implantation Testing (ISO 10993-6 & USP)
Hemocompatibility Testing (ISO 10993-4)
Reproductive & Developmental Toxicity (ISO 10993-3)
Carcinogenicity Testing (ISO 10993-3)
Pyrogenicity Testing
USP Plastics (USP Class IV)
In-Vitro Cytotoxicity Testing (ISO 10993-5)
In-Vitro Genotoxicity Testing (ISO 10993-5)
Sterility
Bioburden Testing
Bacterial Endotoxin Testing
Alternative to Animal Models
Chemical Characterization (ISO 10993-18)
Comprehensive Biological and Toxicological Risk Assessment (ISO 10993-17)
Extractables & Leachables Studies
Impurity / Degradant Toxicity Assessment
Regulatory Documentation & Performance Testing
Biological Evaluation Plans (BEP) & Reports (BER)
Clinical Testing Support
Performance Testing of Devices
Package Testing (ISO 11607 compliance)
Electronic Safety Testing (EMI/EMC)
Risk Assessment & Compliance Support (ISO 14971)
Edit Template
Discovery Chemistry
Discovery Biology
Regulatory Support
In vivo
In vitro
Toxicology
CMC(Chemistry, Manufacturing & Controls) & Formulation
API process development & scale-up
Solid-state & formulation science
Formulation development
Excipients selection & compatibility
Stability & shelf-life studies
Analytics & Bioanalytical Chemistry
Analytics method development & validation(ICH Q2)
Impurity profiling & quantitation
Residual solvents & elemental impurities (ICH Q3C / Q3D)
Dissolution, content uniformity, assay, potency
Batch release testing, CoA, stability-indicating methods
Specialized Routine Testing
Enzyme activity assays (standardized QC panels)
Heparin potency & purity testing
Low Molecular Weight Heparin (LMWH) assays including Enoxaparin
Non-clinical PK studies PK/PD studies & modelling
Efficacy (disease) models Dose-range finding and proof-of-concept studies
Biodistribution & mass-balance (ADME) studies
In vivo DDI/interaction confirmation t
Target validation & target engagement
Cell-based functional assays
In vitro ADME (DMPK)
Permeability & transporter assays
In vitro mechanistic safety screens
Biomarker & PD assay development
Clinical pathology & biomarker panels
GLP bioanalysis / LC-MS/MS capabilities
Biostatistics, data analysis, PK/PD & modelling teams
Drug-drug interaction (DDI) studies
Non-Clinical Safety Testing
In vitro genotoxicity
GLP toxicology studies
Genotoxicity & carcinogenicity
Reproductive & developmental toxicity
Immunotoxicity, hypersensitivity & local tolerance
Histopathology & toxicologic pathology
Impurity toxicology & metabolite safety assessments
Regulatory strategy & agency interaction support
ICH guideline compliance & CTD compilation
Impurity qualification & safety-related assessments
Environmental Risk Assessment (ERA)
Edit Template
In Vivo Animal Studies
Microbiology Testing
Biopharmaceutical Characterization & Functional Assays
Cellular & Molecular Lab Assays
Acute toxicity studies
Sub-acute and sub-chronic toxicity studies
Chronic toxicity studies
Maximum tolerated dose (MTD) determination
Dose range finding (DRF) studies
Pharmacokinetic (PK) and bioavailability studies
Disease and efficacy models
Repeated dose toxicity assessments
Microbiology & Resistance Studies
Sterility testing (per ISO, USP, or pharmacopeial standards)
Bioburden determination and monitoring
Endotoxin testing (Limulus Amebocyte Lysate, LAL)
Antibacterial and antifungal activity assays
Microbial identification / strain typing
Resistance profile screening
Environmental monitoring (surfaces, air, water)
Preservative efficacy (challenge test)
Cell-based & Functional Bioassays (Potency, Immunogenicity, Cytotoxicity)
Mechanism of Action Studies (Receptor Binding, Signal Transduction)
Molecular & Analytical Characterization (HCP, Residual DNA/RNA, Binding Studies)
In Vitro ADME & Stability Studies (Serum/Plasma Stability, Permeability, Protein Degradation)
Stability & Shelf-life Studies (Accelerated, Real-Time, Forced Degradation)
Immunology & Bioanalytical Platforms (Cytokine Release, Immunophenotyping, PK/PD Analysis)
Pathology, Microbiology & Virology Support (Histopathology, Sterility, Mycoplasma, Endotoxin Testing)
Custom Assay Development & Validation
Cytotoxicity Assays (MTT, XTT, LDH, WST-1, Neutral Red)
Cell Proliferation and Apoptosis Studies
Genetic Toxicology Tests (Ames Test, Micronucleus Assay, Chromosome Aberration)
ADME Cellular Models (Caco-2 Permeability, Hepatocyte Metabolism)
Reporter Gene Assays (Mechanism-of-Action)
Flow Cytometry-based Immunophenotyping
Custom Cell-Based Assay Development
Edit Template
Safety & Toxicological Testing
Clinical, Efficacy, and Mechanistic Studies
Purity & Stability Testing
Skin Irritation and Sensitization (OECD 404, LLNA)
Eye Irritation and Corrosion (BCOP, ICE)
Phototoxicity and Photoallergenicity
Acute and Repeated Dose Toxicity
Mutagenicity and Genotoxicity (Ames test, Micronucleus)
Dermal Absorption Studies
Preservative Efficacy Challenge Test
Microbial Limits and Endotoxin Testing
Heavy Metals and Residual Solvent Analysis
Analysis of Restricted and Prohibited Substances
Dermatological Safety: Patch Tests (HRIPT, Cumulative Irritation)
Clinical Efficacy: Moisturization, Anti-aging, Skin Brightening, Anti-acne, Hair Growth
Discovery Biology: Collagen/Elastin Synthesis, Melanin Inhibition, Anti-inflammatory Assays
Microbiome Modulation and Bioassays
In Vitro ADME & Permeation: Skin Absorption, Barrier Function
Custom Assay Development & Claim Validation
Purity, Impurities & Stability Testing (ICH & USP guidelines)
Physical Properties: pH, Viscosity, Spreadability, Particle Size, Zeta Potential
Ingredient Profiling (HPLC, LC-MS, GC-MS, NMR)
Shelf-life and Photostability Testing
Edit Template
Physicochemical Characterization
Biological Efficacy
Toxicology Studies
Regulatory Support
Purity & Impurity Profiling
Physicochemical Property Testing
Solubility, Vapor Pressure, Partition Coefficient, Stability
Spectroscopic & Analytical Method Development (HPLC, GC, MS, NMR)
Viscosity, Particle Size, Zeta Potential
Microbiology & Resistance Studies
Bioactivity & Efficacy Testing (antibacterial, antifungal, insecticidal, herbicidal)
In Vivo Toxicology Studies
Genotoxicity Testing
Ecotoxicity Testing
Impurity / Degradant Toxicity Assessment
Stability & Shelf-Life Studies
Chemical Risk & Exposure Assessment
Custom Assay Development & Validation
Edit Template
Preclinical Efficacy & Mechanistic Studies
Toxicology & Safety Assessment
Regulatory & Compliance Support
In vivo Nutraceutical Efficacy
Glycemic Index & Glycemic Load Estimation
In vitro Nutraceutical Bioactivity
Probiotics
Custom Study Designs
Acute Oral Toxicity Studies
Sub-chronic Toxicity Studies
Genotoxicity Testing
Reproductive & Developmental Toxicity
Skin & Mucosal Irritation Testing
Toxicological Risk Assessment
Novel Food & Dietary Ingredient Submissions
Nutritional Label Validation & Claims Substantiation
Risk Assessment
Edit Template
Contact Us
Request Quote
Home
About
Services
MEDICAL DEVICES
PHARMACEUTICALS
BIOPHARMACEUTICALS
COSMETICS
AGROCHEMICAL
NUTRACEUTICALS
Biocompatibility & Safety Testing
Chemical Characterization & Risk Assessment
Regulatory & Performance Testing
Biocompatibility Tests:
Systemic Toxicity (ISO 10993-11)
Irritation & Sensitization (ISO 10993-10 & USP)
Implantation Testing (ISO 10993-6 & USP)
Hemocompatibility Testing (ISO 10993-4)
Reproductive & Developmental Toxicity (ISO 10993-3)
Carcinogenicity Testing (ISO 10993-3)
Pyrogenicity Testing
USP Plastics (USP Class IV)
In-Vitro Cytotoxicity Testing (ISO 10993-5)
In-Vitro Genotoxicity Testing (ISO 10993-5)
Sterility
Bioburden Testing
Bacterial Endotoxin Testing
Alternative to Animal Models
Chemical Characterization (ISO 10993-18)
Comprehensive Biological and Toxicological Risk Assessment (ISO 10993-17)
Extractables & Leachables Studies
Impurity / Degradant Toxicity Assessment
Regulatory Documentation & Performance Testing
Biological Evaluation Plans (BEP) & Reports (BER)
Clinical Testing Support
Performance Testing of Devices
Package Testing (ISO 11607 compliance)
Electronic Safety Testing (EMI/EMC)
Risk Assessment & Compliance Support (ISO 14971)
Edit Template
Discovery Chemistry
Discovery Biology
Regulatory Support
In vivo
In vitro
Toxicology
CMC(Chemistry, Manufacturing & Controls) & Formulation
API process development & scale-up
Solid-state & formulation science
Formulation development
Excipients selection & compatibility
Stability & shelf-life studies
Analytics & Bioanalytical Chemistry
Analytics method development & validation(ICH Q2)
Impurity profiling & quantitation
Residual solvents & elemental impurities (ICH Q3C / Q3D)
Dissolution, content uniformity, assay, potency
Batch release testing, CoA, stability-indicating methods
Specialized Routine Testing
Enzyme activity assays (standardized QC panels)
Heparin potency & purity testing
Low Molecular Weight Heparin (LMWH) assays including Enoxaparin
Non-clinical PK studies PK/PD studies & modelling
Efficacy (disease) models Dose-range finding and proof-of-concept studies
Biodistribution & mass-balance (ADME) studies
In vivo DDI/interaction confirmation t
Target validation & target engagement
Cell-based functional assays
In vitro ADME (DMPK)
Permeability & transporter assays
In vitro mechanistic safety screens
Biomarker & PD assay development
Clinical pathology & biomarker panels
GLP bioanalysis / LC-MS/MS capabilities
Biostatistics, data analysis, PK/PD & modelling teams
Drug-drug interaction (DDI) studies
Non-Clinical Safety Testing
In vitro genotoxicity
GLP toxicology studies
Genotoxicity & carcinogenicity
Reproductive & developmental toxicity
Immunotoxicity, hypersensitivity & local tolerance
Histopathology & toxicologic pathology
Impurity toxicology & metabolite safety assessments
Regulatory strategy & agency interaction support
ICH guideline compliance & CTD compilation
Impurity qualification & safety-related assessments
Environmental Risk Assessment (ERA)
Edit Template
In Vivo Animal Studies
Microbiology Testing
Biopharmaceutical Characterization & Functional Assays
Cellular & Molecular Lab Assays
Acute toxicity studies
Sub-acute and sub-chronic toxicity studies
Chronic toxicity studies
Maximum tolerated dose (MTD) determination
Dose range finding (DRF) studies
Pharmacokinetic (PK) and bioavailability studies
Disease and efficacy models
Repeated dose toxicity assessments
Microbiology & Resistance Studies
Sterility testing (per ISO, USP, or pharmacopeial standards)
Bioburden determination and monitoring
Endotoxin testing (Limulus Amebocyte Lysate, LAL)
Antibacterial and antifungal activity assays
Microbial identification / strain typing
Resistance profile screening
Environmental monitoring (surfaces, air, water)
Preservative efficacy (challenge test)
Cell-based & Functional Bioassays (Potency, Immunogenicity, Cytotoxicity)
Mechanism of Action Studies (Receptor Binding, Signal Transduction)
Molecular & Analytical Characterization (HCP, Residual DNA/RNA, Binding Studies)
In Vitro ADME & Stability Studies (Serum/Plasma Stability, Permeability, Protein Degradation)
Stability & Shelf-life Studies (Accelerated, Real-Time, Forced Degradation)
Immunology & Bioanalytical Platforms (Cytokine Release, Immunophenotyping, PK/PD Analysis)
Pathology, Microbiology & Virology Support (Histopathology, Sterility, Mycoplasma, Endotoxin Testing)
Custom Assay Development & Validation
Cytotoxicity Assays (MTT, XTT, LDH, WST-1, Neutral Red)
Cell Proliferation and Apoptosis Studies
Genetic Toxicology Tests (Ames Test, Micronucleus Assay, Chromosome Aberration)
ADME Cellular Models (Caco-2 Permeability, Hepatocyte Metabolism)
Reporter Gene Assays (Mechanism-of-Action)
Flow Cytometry-based Immunophenotyping
Custom Cell-Based Assay Development
Edit Template
Safety & Toxicological Testing
Clinical, Efficacy, and Mechanistic Studies
Purity & Stability Testing
Skin Irritation and Sensitization (OECD 404, LLNA)
Eye Irritation and Corrosion (BCOP, ICE)
Phototoxicity and Photoallergenicity
Acute and Repeated Dose Toxicity
Mutagenicity and Genotoxicity (Ames test, Micronucleus)
Dermal Absorption Studies
Preservative Efficacy Challenge Test
Microbial Limits and Endotoxin Testing
Heavy Metals and Residual Solvent Analysis
Analysis of Restricted and Prohibited Substances
Dermatological Safety: Patch Tests (HRIPT, Cumulative Irritation)
Clinical Efficacy: Moisturization, Anti-aging, Skin Brightening, Anti-acne, Hair Growth
Discovery Biology: Collagen/Elastin Synthesis, Melanin Inhibition, Anti-inflammatory Assays
Microbiome Modulation and Bioassays
In Vitro ADME & Permeation: Skin Absorption, Barrier Function
Custom Assay Development & Claim Validation
Purity, Impurities & Stability Testing (ICH & USP guidelines)
Physical Properties: pH, Viscosity, Spreadability, Particle Size, Zeta Potential
Ingredient Profiling (HPLC, LC-MS, GC-MS, NMR)
Shelf-life and Photostability Testing
Edit Template
Physicochemical Characterization
Biological Efficacy
Toxicology Studies
Regulatory Support
Purity & Impurity Profiling
Physicochemical Property Testing
Solubility, Vapor Pressure, Partition Coefficient, Stability
Spectroscopic & Analytical Method Development (HPLC, GC, MS, NMR)
Viscosity, Particle Size, Zeta Potential
Microbiology & Resistance Studies
Bioactivity & Efficacy Testing (antibacterial, antifungal, insecticidal, herbicidal)
In Vivo Toxicology Studies
Genotoxicity Testing
Ecotoxicity Testing
Impurity / Degradant Toxicity Assessment
Stability & Shelf-Life Studies
Chemical Risk & Exposure Assessment
Custom Assay Development & Validation
Edit Template
Preclinical Efficacy & Mechanistic Studies
Toxicology & Safety Assessment
Regulatory & Compliance Support
In vivo Nutraceutical Efficacy
Glycemic Index & Glycemic Load Estimation
In vitro Nutraceutical Bioactivity
Probiotics
Custom Study Designs
Acute Oral Toxicity Studies
Sub-chronic Toxicity Studies
Genotoxicity Testing
Reproductive & Developmental Toxicity
Skin & Mucosal Irritation Testing
Toxicological Risk Assessment
Novel Food & Dietary Ingredient Submissions
Nutritional Label Validation & Claims Substantiation
Risk Assessment
Edit Template
Contact Us
Request Quote
Home
About
Services
MEDICAL DEVICES
PHARMACEUTICALS
BIOPHARMACEUTICALS
COSMETICS
AGROCHEMICAL
NUTRACEUTICALS
Biocompatibility & Safety Testing
Chemical Characterization & Risk Assessment
Regulatory & Performance Testing
Biocompatibility Tests:
Systemic Toxicity (ISO 10993-11)
Irritation & Sensitization (ISO 10993-10 & USP)
Implantation Testing (ISO 10993-6 & USP)
Hemocompatibility Testing (ISO 10993-4)
Reproductive & Developmental Toxicity (ISO 10993-3)
Carcinogenicity Testing (ISO 10993-3)
Pyrogenicity Testing
USP Plastics (USP Class IV)
In-Vitro Cytotoxicity Testing (ISO 10993-5)
In-Vitro Genotoxicity Testing (ISO 10993-5)
Sterility
Bioburden Testing
Bacterial Endotoxin Testing
Alternative to Animal Models
Chemical Characterization (ISO 10993-18)
Comprehensive Biological and Toxicological Risk Assessment (ISO 10993-17)
Extractables & Leachables Studies
Impurity / Degradant Toxicity Assessment
Regulatory Documentation & Performance Testing
Biological Evaluation Plans (BEP) & Reports (BER)
Clinical Testing Support
Performance Testing of Devices
Package Testing (ISO 11607 compliance)
Electronic Safety Testing (EMI/EMC)
Risk Assessment & Compliance Support (ISO 14971)
Edit Template
Discovery Chemistry
Discovery Biology
Regulatory Support
In vivo
In vitro
Toxicology
CMC(Chemistry, Manufacturing & Controls) & Formulation
API process development & scale-up
Solid-state & formulation science
Formulation development
Excipients selection & compatibility
Stability & shelf-life studies
Analytics & Bioanalytical Chemistry
Analytics method development & validation(ICH Q2)
Impurity profiling & quantitation
Residual solvents & elemental impurities (ICH Q3C / Q3D)
Dissolution, content uniformity, assay, potency
Batch release testing, CoA, stability-indicating methods
Specialized Routine Testing
Enzyme activity assays (standardized QC panels)
Heparin potency & purity testing
Low Molecular Weight Heparin (LMWH) assays including Enoxaparin
Non-clinical PK studies PK/PD studies & modelling
Efficacy (disease) models Dose-range finding and proof-of-concept studies
Biodistribution & mass-balance (ADME) studies
In vivo DDI/interaction confirmation t
Target validation & target engagement
Cell-based functional assays
In vitro ADME (DMPK)
Permeability & transporter assays
In vitro mechanistic safety screens
Biomarker & PD assay development
Clinical pathology & biomarker panels
GLP bioanalysis / LC-MS/MS capabilities
Biostatistics, data analysis, PK/PD & modelling teams
Drug-drug interaction (DDI) studies
Non-Clinical Safety Testing
In vitro genotoxicity
GLP toxicology studies
Genotoxicity & carcinogenicity
Reproductive & developmental toxicity
Immunotoxicity, hypersensitivity & local tolerance
Histopathology & toxicologic pathology
Impurity toxicology & metabolite safety assessments
Regulatory strategy & agency interaction support
ICH guideline compliance & CTD compilation
Impurity qualification & safety-related assessments
Environmental Risk Assessment (ERA)
Edit Template
In Vivo Animal Studies
Microbiology Testing
Biopharmaceutical Characterization & Functional Assays
Cellular & Molecular Lab Assays
Acute toxicity studies
Sub-acute and sub-chronic toxicity studies
Chronic toxicity studies
Maximum tolerated dose (MTD) determination
Dose range finding (DRF) studies
Pharmacokinetic (PK) and bioavailability studies
Disease and efficacy models
Repeated dose toxicity assessments
Microbiology & Resistance Studies
Sterility testing (per ISO, USP, or pharmacopeial standards)
Bioburden determination and monitoring
Endotoxin testing (Limulus Amebocyte Lysate, LAL)
Antibacterial and antifungal activity assays
Microbial identification / strain typing
Resistance profile screening
Environmental monitoring (surfaces, air, water)
Preservative efficacy (challenge test)
Cell-based & Functional Bioassays (Potency, Immunogenicity, Cytotoxicity)
Mechanism of Action Studies (Receptor Binding, Signal Transduction)
Molecular & Analytical Characterization (HCP, Residual DNA/RNA, Binding Studies)
In Vitro ADME & Stability Studies (Serum/Plasma Stability, Permeability, Protein Degradation)
Stability & Shelf-life Studies (Accelerated, Real-Time, Forced Degradation)
Immunology & Bioanalytical Platforms (Cytokine Release, Immunophenotyping, PK/PD Analysis)
Pathology, Microbiology & Virology Support (Histopathology, Sterility, Mycoplasma, Endotoxin Testing)
Custom Assay Development & Validation
Cytotoxicity Assays (MTT, XTT, LDH, WST-1, Neutral Red)
Cell Proliferation and Apoptosis Studies
Genetic Toxicology Tests (Ames Test, Micronucleus Assay, Chromosome Aberration)
ADME Cellular Models (Caco-2 Permeability, Hepatocyte Metabolism)
Reporter Gene Assays (Mechanism-of-Action)
Flow Cytometry-based Immunophenotyping
Custom Cell-Based Assay Development
Edit Template
Safety & Toxicological Testing
Clinical, Efficacy, and Mechanistic Studies
Purity & Stability Testing
Skin Irritation and Sensitization (OECD 404, LLNA)
Eye Irritation and Corrosion (BCOP, ICE)
Phototoxicity and Photoallergenicity
Acute and Repeated Dose Toxicity
Mutagenicity and Genotoxicity (Ames test, Micronucleus)
Dermal Absorption Studies
Preservative Efficacy Challenge Test
Microbial Limits and Endotoxin Testing
Heavy Metals and Residual Solvent Analysis
Analysis of Restricted and Prohibited Substances
Dermatological Safety: Patch Tests (HRIPT, Cumulative Irritation)
Clinical Efficacy: Moisturization, Anti-aging, Skin Brightening, Anti-acne, Hair Growth
Discovery Biology: Collagen/Elastin Synthesis, Melanin Inhibition, Anti-inflammatory Assays
Microbiome Modulation and Bioassays
In Vitro ADME & Permeation: Skin Absorption, Barrier Function
Custom Assay Development & Claim Validation
Purity, Impurities & Stability Testing (ICH & USP guidelines)
Physical Properties: pH, Viscosity, Spreadability, Particle Size, Zeta Potential
Ingredient Profiling (HPLC, LC-MS, GC-MS, NMR)
Shelf-life and Photostability Testing
Edit Template
Physicochemical Characterization
Biological Efficacy
Toxicology Studies
Regulatory Support
Purity & Impurity Profiling
Physicochemical Property Testing
Solubility, Vapor Pressure, Partition Coefficient, Stability
Spectroscopic & Analytical Method Development (HPLC, GC, MS, NMR)
Viscosity, Particle Size, Zeta Potential
Microbiology & Resistance Studies
Bioactivity & Efficacy Testing (antibacterial, antifungal, insecticidal, herbicidal)
In Vivo Toxicology Studies
Genotoxicity Testing
Ecotoxicity Testing
Impurity / Degradant Toxicity Assessment
Stability & Shelf-Life Studies
Chemical Risk & Exposure Assessment
Custom Assay Development & Validation
Edit Template
Preclinical Efficacy & Mechanistic Studies
Toxicology & Safety Assessment
Regulatory & Compliance Support
In vivo Nutraceutical Efficacy
Glycemic Index & Glycemic Load Estimation
In vitro Nutraceutical Bioactivity
Probiotics
Custom Study Designs
Acute Oral Toxicity Studies
Sub-chronic Toxicity Studies
Genotoxicity Testing
Reproductive & Developmental Toxicity
Skin & Mucosal Irritation Testing
Toxicological Risk Assessment
Novel Food & Dietary Ingredient Submissions
Nutritional Label Validation & Claims Substantiation
Risk Assessment
Edit Template
Contact Us
Request Quote
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