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Pharmaceutical

Pharmaceutical

Supporting pharmaceutical quality in highly regulated environments through testing aligned with global frameworks, using methodologies based on USP, BP, Ph. Eur., and ISO standards.

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Large PNAC Accredited
Testing Scope

Comprehensive analytical solutions for pharmaceutical quality, safety, and compliance

We offer advanced analytical capabilities across pharmaceuticals, nutraceuticals, cosmeceuticals, medical devices, and pharma-grade packaging systems, enabling precise quality control and compliance with both local and international regulatory requirements.

We offer advanced analytical capabilities across pharmaceuticals, nutraceuticals, cosmeceuticals, medical devices, and pharma-grade packaging systems, enabling precise quality control and compliance with both local and international regulatory requirements.

Raw Material, APIs, Finished and R&D Products

Cosmetics, Dermatological and Skincare Products

Herbal Extracts and Nutraceutical Raw Material

Surgical Instruments and Medical Devices

Pharmaceutical Testing and
Analytical Services

Pharmaceutical Testing and Analytical Services

Comprehensive pharmaceutical testing across raw materials, APIs, excipients, and finished dosage forms, designed to support product quality, safety, and regulatory compliance at every stage of development and production.

Our analytical capabilities combine advanced instrumentation with validated methodologies to deliver precise, reproducible, and audit-ready results aligned with global pharmacopeial and regulatory standards.

  • Highly-qualified technical and QA/QC experts

  • Dedicated team for regulatory and technical support

  • Test reports supporting national/international regulatory requirements

Advanced Analytical Instrumentation:
HPLC (UV/Vis, DAD, MS/MS), LC-MS/MS, Single Quads, Triple Quads, GC-FID, GC-MS, HS-GC-MS, AAS, ICP-OES, ICP-MS, UV/Vis, FTIR, ELISA Kits

Comprehensive pharmaceutical testing across raw materials, APIs, excipients, and finished dosage forms, designed to support product quality, safety, and regulatory compliance at every stage of development and production.

Our analytical capabilities combine advanced instrumentation with validated methodologies to deliver precise, reproducible, and audit-ready results aligned with global pharmacopeial and regulatory standards.

  • Highly-qualified technical and QA/QC experts

  • Dedicated team for regulatory and technical support

  • Test reports supporting national/international regulatory requirements

Advanced Analytical Instrumentation:
HPLC (UV/Vis, DAD, MS/MS), LC-MS/MS, Single Quads, Triple Quads, GC-FID, GC-MS, HS-GC-MS, AAS, ICP-OES, ICP-MS, UV/Vis, FTIR, ELISA Kits

API & Product Assay

Verifying active ingredient potency and ensuring precise therapeutic dosing

Accurate quantitative determination of active pharmaceutical ingredients (APls) in raw materials and finished dosage forms to verify label claim, product potency and compliance with pharmacopeial specifications.

  • Assay / Purity

  • Qualitative & Quantitative Analysis based on Liquid and Gas Chromatography

  • Spectrophotometric Identification

  • FTIR Material Identification

API & Product Assay

Verifying active ingredient potency and ensuring precise therapeutic dosing

Accurate quantitative determination of active pharmaceutical ingredients (APls) in raw materials and finished dosage forms to verify label claim, product potency and compliance with pharmacopeial specifications.

  • Assay / Purity

  • Qualitative & Quantitative Analysis based on Liquid and Gas Chromatography

  • Spectrophotometric Identification

  • FTIR Material Identification

API & Product Assay

Verifying active ingredient potency and ensuring precise therapeutic dosing

Accurate quantitative determination of active pharmaceutical ingredients (APls) in raw materials and finished dosage forms to verify label claim, product potency and compliance with pharmacopeial specifications.

  • Assay / Purity

  • Qualitative & Quantitative Analysis based on Liquid and Gas Chromatography

  • Spectrophotometric Identification

  • FTIR Material Identification

Impurities & Contaminant Testing

Identification and quantification of the process-related and degradation-related impurities

  • DEG / EG Detection in Solvents

  • Nitrosamines (NDMA / NDEA) Detection

  • 1-Methyl-4-Nitrosopiperazine (MeNP) Detection

  • Volatile Organic Compounds (VOCs)

  • Organic Impurities of APIs

  • Phthalates 

  • Phenols & Alkylphenols / APEOs

  • Chlorophenols & Chlorinated Compounds

  • Polycyclic Aromatic Hydrocarbons (PAHs)


  • Residual Solvents Analysis, ICH Q3C (R8) compliant

  • Elemental Impurities (Pb, Cd, As, Hg, Sb, Cr, Cr(VI), Co, Cu, Ni, Se, Sn, Zn)

Impurities & Contaminant Testing

Identification and quantification of the process-related and degradation-related impurities

  • DEG / EG Detection in Solvents

  • Nitrosamines (NDMA / NDEA) Detection

  • 1-Methyl-4-Nitrosopiperazine (MeNP) Detection

  • Volatile Organic Compounds (VOCs)

  • Organic Impurities of APIs

  • Phthalates 

  • Phenols & Alkylphenols / APEOs

  • Chlorophenols & Chlorinated Compounds

  • Polycyclic Aromatic Hydrocarbons (PAHs)


  • Residual Solvents Analysis, ICH Q3C (R8) compliant

  • Elemental Impurities (Pb, Cd, As, Hg, Sb, Cr, Cr(VI), Co, Cu, Ni, Se, Sn, Zn)

Impurities & Contaminant Testing

Identification and quantification of the process-related and degradation-related impurities

  • DEG / EG Detection in Solvents

  • Nitrosamines (NDMA / NDEA) Detection

  • 1-Methyl-4-Nitrosopiperazine (MeNP) Detection

  • Volatile Organic Compounds (VOCs)

  • Organic Impurities of APIs

  • Phthalates 

  • Phenols & Alkylphenols / APEOs

  • Chlorophenols & Chlorinated Compounds

  • Polycyclic Aromatic Hydrocarbons (PAHs)


  • Residual Solvents Analysis, ICH Q3C (R8) compliant

  • Elemental Impurities (Pb, Cd, As, Hg, Sb, Cr, Cr(VI), Co, Cu, Ni, Se, Sn, Zn)

Stability & Shelf-Life Studies

ICH-compliant studies to evaluate the physical, chemical, and microbiological stability of pharma products

  • Stability Studies

  • Shelf-Life Determination

  • Real-Time & Accelerated Stability Studies


Stability & Shelf-Life Studies

ICH-compliant studies to evaluate the physical, chemical, and microbiological stability of pharma products

  • Stability Studies

  • Shelf-Life Determination

  • Real-Time & Accelerated Stability Studies


Stability & Shelf-Life Studies

ICH-compliant studies to evaluate the physical, chemical, and microbiological stability of pharma products

  • Stability Studies

  • Shelf-Life Determination

  • Real-Time & Accelerated Stability Studies


Pharmaceutical Microbiological Testing

Comprehensive microbiological quality assessment for sterile & non-sterile pharma products

  • Pathogens Detection

  • Microbial Limit Test

  • Sterility Testing

  • Bacterial Endotoxin Testing (LAL)

  • Bioburden Testing

  • Antimicrobial / Disinfectant Efficacy Testing

  • Preservative Efficacy Testing

  • Environmental Monitoring

  • Swab Testing for Microbial Contamination

Pharmaceutical Microbiological Testing

Comprehensive microbiological quality assessment for sterile & non-sterile pharma products

  • Pathogens Detection

  • Microbial Limit Test

  • Sterility Testing

  • Bacterial Endotoxin Testing (LAL)

  • Bioburden Testing

  • Antimicrobial / Disinfectant Efficacy Testing

  • Preservative Efficacy Testing

  • Environmental Monitoring

  • Swab Testing for Microbial Contamination

Pharmaceutical Microbiological Testing

Comprehensive microbiological quality assessment for sterile & non-sterile pharma products

  • Pathogens Detection

  • Microbial Limit Test

  • Sterility Testing

  • Bacterial Endotoxin Testing (LAL)

  • Bioburden Testing

  • Antimicrobial / Disinfectant Efficacy Testing

  • Preservative Efficacy Testing

  • Environmental Monitoring

  • Swab Testing for Microbial Contamination

Method Development & Validation

Development and validation of robust analytical methods in accordance with ICH and pharmacopoeial guidelines

  • Analytical Method Development

  • Method Verification Studies

  • Method Validation

Method Development & Validation

Development and validation of robust analytical methods in accordance with ICH and pharmacopoeial guidelines

  • Analytical Method Development

  • Method Verification Studies

  • Method Validation

Method Development & Validation

Development and validation of robust analytical methods in accordance with ICH and pharmacopoeial guidelines

  • Analytical Method Development

  • Method Verification Studies

  • Method Validation

Packaging & Container Compatibility

Specialized E&L studies and closure integrity testing to verify primary packaging compatibility

  • Extractables & Leachables Studies

  • Glass Delamination Testing

  • Packaging Interaction Studies

  • Container Closure Integrity Testing (CCIT)

  • Sterile Packing Test

Packaging & Container Compatibility

Specialized E&L studies and closure integrity testing to verify primary packaging compatibility

  • Extractables & Leachables Studies

  • Glass Delamination Testing

  • Packaging Interaction Studies

  • Container Closure Integrity Testing (CCIT)

  • Sterile Packing Test

Packaging & Container Compatibility

Specialized E&L studies and closure integrity testing to verify primary packaging compatibility

  • Extractables & Leachables Studies

  • Glass Delamination Testing

  • Packaging Interaction Studies

  • Container Closure Integrity Testing (CCIT)

  • Sterile Packing Test

Need more details?

Send us a request

Nutraceutical Testing

Comprehensive analytical testing for nutraceuticals, dietary supplements, and herbal products, supporting identity, potency, purity, label claim verification, and product safety using advanced analytical methodologies.

  • Vitamins & Minerals Estimation

  • Fatty Acid Profiling

  • Nutritional Profiling

  • Heavy Metals Detection

  • Pesticide Residues Analysis

  • Herbal Extracts Analysis

  • Analysis of Henna

  • Shilajit Testing

Cosmeceutical Testing

Advanced analytical testing for cosmetics and cosmeceutical products, delivering scientific evidence of product quality, safety, composition, and performance through comprehensive chemical and microbiological evaluation.

Safety & Toxicological Assessment

Evaluation of cosmeceutical products for potential irritation, allergenicity, and toxicological risk

  • Skin Irritants, Allergens & Toxicology

  • IFRA Allergen Testing

  • Phthalates Detection

  • Heavy Metals Analysis

Safety & Toxicological Assessment

Evaluation of cosmeceutical products for potential irritation, allergenicity, and toxicological risk

  • Skin Irritants, Allergens & Toxicology

  • IFRA Allergen Testing

  • Phthalates Detection

  • Heavy Metals Analysis

Safety & Toxicological Assessment

Evaluation of cosmeceutical products for potential irritation, allergenicity, and toxicological risk

  • Skin Irritants, Allergens & Toxicology

  • IFRA Allergen Testing

  • Phthalates Detection

  • Heavy Metals Analysis

Chemical Composition & Actives Analysis

Identification and quantification of active ingredients, fragrances, and formulation components

  • Active Ingredients Analysis (Vitamins, Minerals & Antioxidants)

  • Menthol Analysis

  • Fragrance & Volatile Components (GC-MS for perfumes)

  • Henna & Hair Dye Purity (PPD Content, Heavy Metals)

Chemical Composition & Actives Analysis

Identification and quantification of active ingredients, fragrances, and formulation components

  • Active Ingredients Analysis (Vitamins, Minerals & Antioxidants)

  • Menthol Analysis

  • Fragrance & Volatile Components (GC-MS for perfumes)

  • Henna & Hair Dye Purity (PPD Content, Heavy Metals)

Chemical Composition & Actives Analysis

Identification and quantification of active ingredients, fragrances, and formulation components

  • Active Ingredients Analysis (Vitamins, Minerals & Antioxidants)

  • Menthol Analysis

  • Fragrance & Volatile Components (GC-MS for perfumes)

  • Henna & Hair Dye Purity (PPD Content, Heavy Metals)

Physicochemical Characterization

Evaluation of formulation properties that influence product stability and user experience

  • pH, Viscosity & Texture Analysis

  • Color Stability & Oxidation Testing (Makeup)

Physicochemical Characterization

Evaluation of formulation properties that influence product stability and user experience

  • pH, Viscosity & Texture Analysis

  • Color Stability & Oxidation Testing (Makeup)

Physicochemical Characterization

Evaluation of formulation properties that influence product stability and user experience

  • pH, Viscosity & Texture Analysis

  • Color Stability & Oxidation Testing (Makeup)

Product Performance & Functional Testing

Verification of product claims and performance

  • SPF Testing (Sunscreens & Sunblock)

  • Foaming & Cleansing Efficacy (Soaps, Face Washes)

  • Free Caustic Alkali

Product Performance & Functional Testing

Verification of product claims and performance

  • SPF Testing (Sunscreens & Sunblock)

  • Foaming & Cleansing Efficacy (Soaps, Face Washes)

  • Free Caustic Alkali

Product Performance & Functional Testing

Verification of product claims and performance

  • SPF Testing (Sunscreens & Sunblock)

  • Foaming & Cleansing Efficacy (Soaps, Face Washes)

  • Free Caustic Alkali

Complete Microbiological Testing

Verification of microbial safety of all types of cosmetics and skincare products

  • Pathogen Detection

  • Microbial Limit Testing

  • Preservative Efficacy Testing (PET)

  • Bioburden Testing

  • Environmental Monitoring

  • Stability-Linked Microbial Assessment

Complete Microbiological Testing

Verification of microbial safety of all types of cosmetics and skincare products

  • Pathogen Detection

  • Microbial Limit Testing

  • Preservative Efficacy Testing (PET)

  • Bioburden Testing

  • Environmental Monitoring

  • Stability-Linked Microbial Assessment

Complete Microbiological Testing

Verification of microbial safety of all types of cosmetics and skincare products

  • Pathogen Detection

  • Microbial Limit Testing

  • Preservative Efficacy Testing (PET)

  • Bioburden Testing

  • Environmental Monitoring

  • Stability-Linked Microbial Assessment

Surgical & Medical Devices Testing

Testing to verify the safety, sterility, biocompatibility, and functional performance of medical devices and surgical products, such as: surgical instruments, syringes and needles, catheters, implants, surgical gloves, wound dressings, infusion sets, and diagnostic devices.

Sterility & Microbiological Testing

  • Bacterial Endotoxin (LAL) Testing

  • Bioburden Testing

Material & Chemical Safety

  • Extractables & Leachables Studies

  • Residual Analysis

  • Elemental Impurities Testing

Packaging & Sterile Barrier Testing

  • Sterile Packing Test

  • Container Closure Integrity

Performance & Functional Testing

  • Mechanical Strength Testing

  • Dimensional Verification

PNAC accredited
ISO/IEC 17025 testing lab

PNAC accredited
ISO/IEC 17025 testing lab

PNAC accredited
ISO/IEC 17025 testing lab

U.S. IAC Certified Microbiology Lab

U.S. IAC Certified Microbiology Lab

Pakistan’s first third-party lab, approved for ISO Class 5 & 7 standards

Pakistan’s first third-party lab, approved for ISO Class 5 & 7 standards

How testing works

Five steps from your first message to an accredited report.

Step 01

You

Request

For a quote, include:

The product and quantity

Test standard or buyer requirement

Destination market

Your deadline

Send us a request

Step 02

Tti Labs

Quote

Each test and its charge in writing, with the turnaround confirmed, before any work starts.

Step 03

You

Send sample

Drop off

Our laboratory in Lahore

Collection

Arranged by customer service

Step 04

Tti Labs

Testing

Every sample follows a fully traceable workflow with secure chain-of-custody controls.

~1500

tests a day

600+

samples a day

Step 05

Tti Labs

Report

ISO/IEC 17025 accredited report, within the turnaround in your quotation.

How testing works

Five steps from your first message to an accredited report.

Step 01

You

Request

For a quote, include:

The product and quantity

Test standard or buyer requirement

Destination market

Your deadline

Send us a request

Step 02

Tti Labs

Quote

Each test and its charge in writing, with the turnaround confirmed, before any work starts.

Step 03

You

Send sample

Drop off

Our laboratory in Lahore

Collection

Arranged by customer service

Step 04

Tti Labs

Testing

Every sample follows a fully traceable workflow with secure chain-of-custody controls.

~1500

tests a day

600+

samples a day

Step 05

Tti Labs

Report

ISO/IEC 17025 accredited report, within the turnaround in your quotation.

How testing works

Five steps from your first message to an accredited report.

Step 01

You

Request

For a quote, include:

The product and quantity

Test standard or buyer requirement

Destination market

Your deadline

Send us a request

Step 02

Tti Labs

Quote

Each test and its charge in writing, with the turnaround confirmed, before any work starts.

Step 03

You

Send sample

Drop off

Our laboratory in Lahore

Collection

Arranged by customer service

Step 04

Tti Labs

Testing

Every sample follows a fully traceable workflow with secure chain-of-custody controls.

~1500

tests a day

600+

samples a day

Step 05

Tti Labs

Report

ISO/IEC 17025 accredited report, within the turnaround in your quotation.

Cover of the Tti Labs Pharmaceutical Testing brochure

Pharmaceutical

Pharmaceutical testing services

12 pages · PDF 4.5 MB

Download brochure

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Why choose Tti as your quality partner?

Why choose Tti as your quality partner?

Partnering with Tti means securing your supply chain through an ISO/IEC 17025 accredited authority, trusted by 1500+ global brands.

Partnering with Tti means securing your supply chain through an
ISO/IEC 17025 accredited authority, trusted by 1500+ global brands.

Partnering with Tti means securing your supply chain through an ISO/IEC 17025 accredited authority, trusted by 1500+ global brands.

We eliminate operational bottlenecks by combining advanced analytical infrastructure with the region's fastest turnaround time and an uncompromising sample chain-of-custody. We provide scientific precision required to clear customs rapidly, delivering cost-effective compliance solutions to prevent product recalls.

We eliminate operational bottlenecks by combining advanced analytical infrastructure with the region's fastest turnaround time and an uncompromising sample chain-of-custody. We provide scientific precision required to clear customs rapidly, delivering cost-effective compliance solutions to prevent product recalls.

You get direct access to technical experts who engineer flexible and scalable QA programs designed around your unique processing lines and variable batch sizes.

You get direct access to technical experts who engineer flexible and scalable QA programs designed around your unique processing lines and variable batch sizes.

Is your testing service ISO/IEC 17025 accredited?

Yes. Tti Testing Laboratories is accredited by the Pakistan National Accreditation Council (PNAC) under ISO/IEC 17025.

Can you validate analytical methods?

Yes. We provide method development, validation, and verification studies.

Can you provide urgent sample testing service?

Yes. We can provide an expedited turnaround through our shuttle service within two working days, subject to a 100% surcharge.

What payment methods are accepted?

Payment terms are specified in the quotation, and 100% advance payment is required. You can pay online, deposit cash in a bank, or pay by cheque.

Do you perform microbiological testing?

Yes. We have a fully equipped microbiological laboratory and perform a range of microbial tests according to the client’s requirements.

Can I receive a chromatogram?

Yes. Chromatograms and supporting analytical data may be provided where agreed in the contract or according to the client’s requirements.

Can I discuss my method with your analyst or technical team before testing?

Yes. Our technical and customer service teams can arrange a discussion to review analytical methods, testing requirements, and project feasibility before sample submission.

What is the standard turnaround time?

After receiving the sample, completed test request form, and payment receipt, we can provide the report within four to five working days. Turnaround times may vary for certain tests, including microbiological testing.

What would you like to know more about our services in Pharmaceutical division?

What would you like to know more about our services in Pharmaceutical division?

What service would you like to inquire? *

What service would you like to inquire? *

For a quote, include the product, quantity, test standard or buyer requirement, destination market and your deadline.

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