Adico Laboratory

ABOUT US

Oniosome Health Care (P) Ltd. was established by a group of pharmaceutical scientist in the year 2010, at Mohali.

The organization was set up with a inputs from industry representatives, Scientists and renowned academicians with a vision to make advancements in the field of formulation development and Analytical Testing.

Target of organization is to develop innovative drug products & delivery systems, Technology transfer and to fulfill all analytical testing requirements of all Pharma, Food, Bio, Agriculture and API industry.

Projects in association with various reputed organizations: BIRAC/SBIRI/DBT/DST, Punjab University, NRDC, IMTECH, NIPER, ICT, Mumbai, IIT etc.

Product Pipeline : Successfully completed or ongoing Nano Particles, Liposomes, Ophthalmic, Oral & Topical Dosage Form etc.

INDUSTRIAL SUPPORT

Formulation & Development

·Conventional & Novel dosage form development: Tablet (Immediate Release, Sustained Release, Multilayered, FDT, Orodispersible, etc.); Capsule (SR), Creams, Gel, Lotion, Ointment, Patch, eye drop,

Nanoparticle, Liposome, Nanofiber Patch, etc.

·In-vitro Studies: All IPQC parameter, Dissolution / permeation studies.

·Technology Transfer, Reverse Engineering of existing products, Tailor made formulations to improve the half-life, solubility, bioavailability and stability of the drug in formulations.

·Regulatory Support: IPR, Copyrights, Trademarks, Dossier, Patent & Patent Evaluation etc.

·Act as an expert consultancy for all stages of product development, scale-up, manufacturing, medical, science-based marketing. Intellectual property support to identify potential drugs & strategic delivery system for development.

Application of Quality by Design (QbD)

Formulation Analytical Lab / Advance Synthesis Lab

HPLC (UV, PDA, RI, UPLC)

Fuming Cupboards

Mass Spectroscopy

Rotatory Evaporators ..

LCMS/Mass/LCMS-MS, BET (Surface Analyzer), Particle Size Analyzer, Spray Dryer, FBD

Hydrogenator,Master size analyzer (Dry & Wet Method)

Lyophilizer, TEM,FESEM, Dissolution type 4 apparatus

GCMS/GC-Head space, Stirrers

XRF, DVS, DSC, TGA, FTIR, XRD, SEM, NMR (C-NMR/HNMR), ICPMS, CHSNO analyzer

Diffusion cell assembly, Hot stage microscope,Milli­Q Water Purifier

Capillary Electrophoresis

Autoclave Portable

Advance Weighing Balance etc.

Laboratory  Homogenizer etc

Analytical Services Provider = 6

Partner Synthesis Labs = 5

THIRD PARTY MANUFACTURING

We are engaged in third party manufacturing and supplying a wide range of formulations such as tablets, capsules, injections, ear & eye drops, ointments and new drugs that are DCGI approved. This range includes Analgesics, Antibiotics, Anti-inflammatory, Anti-bacterial, Anti­microbial, Anti-allergies, Anti-helmintics, Anti-ulcerant and supplements.

We have well developed infrastructure as well as team of qualified and experienced professional to meet the bulk requirements of client. All products are subsequently manufactured and packed in strict accordance to Good manufacturing practice.

HERBAL PRODUCT DEV. & TESTING

  • Extraction, isolation, phytochemical screening,
  • Total phenolic assay, Determination of steroid,
  • Heavy metals analysis, Antioxidant analysis.
  • Essential oil analysis, Quantitative analysis of
    phytoconstituents,
  • Chromatographic finger printing

 

 

COSMETICS PRODUCT DEV. & TESTING

  • Testing as per Bureau of Indian Standards (BIS) requirement.
  • Safety tests like heavy metals in cosmetics, banned colors and banned chemicals.
  • Microbiology testing for microbial counts and pathogens
  • Estimation of active ingredients
  • Functional tests like viscosity, spread-ability, scratch test, pay-off test
  • Skin irritation studies
  • Stability studies for shelf life estimation
  • Complaints investigation and troubleshooting

ANALYTICAL SERVICES

Tested as per USP/BP/EP/IP & Customers Requirements.

Preformulation/Phy./Chem. Parameters :

Solubility, Stability, Melting point, Refractive index, Partition coefficient, Dissociation constant, LOD, viscosity, ash value determi-nation, content uniformity, acid value, peroxide value, optical rotation, etc.

(a)   Analytical method development & validation

(b)   Uniformity of content, Assay, RS analysis of API and Formulation.

(c)   Crystal geometry and Polymorphism analysis, Thermal Analysis, Heavy metals analysis & Element analysis

(f)     Impurity quantification & Residual solvent analysis

(g)    BET surface area & Average porosity analysis

(h)    Particle characterization with D10, D50 & D90 value

Stability Studies: Short term, long term, Accelerated Stability Studies as per ICH guideline (40°C/75% RH; 25°C/60% RH)

Impurities Synthesis & Profile

 

MICROBIOLOGICAL TESTING

  • Identification and characterization of microorganism
  • Antibiotic assay, Microbial limit test
  • Microbiological testing of API, finished dosage form
  • Detection & Identification of Pathogens
  • Total Microbial Count, Pathogen Detection, In vitro MIC Screening

Website : www.oniosome.com

Oniosome Healthcare Private Limited Infrastructure

Analytical Lab

Advance Synthesis Lab

HPLC (UV, PDA, RI)

Fuming Cupboards

Mass Spectroscopy

Rotatory Evaporators

LCMS/Mass/LCMS-MS, BET (surface analyzer)

Hydrogenator, Master size analyzer (Dry & Wet Method)

Lyophilizer, TEM, FESEM, Dissolution type 4 apparatus

GCMS/GC-Head space, Stirrers

UPLC, DVS, DSC, TGA, FTIR, XRD, SEM, NMR (C-NMR/HNMR), ICPMS, CHSNO analyzer

Diffusion cell assembly, Hot stage microscope, Milli-Q Water Purifier

Capillary Electrophoresis

Autoclave Portable

Advance Weighing Balance etc.

Laboratory Homogenizer etc

Analytical Services Provider = 6      Partner Synthesis Labs = 5

Microbiological Testing

  • Identification and characterization of
    microorganism
  • Antibiotic assay, Microbial limit test
  • Microbiological testing of API, finished dosage form
  • Detection & Identification of Pathogens
  • Total Microbial Count, Pathogen Detection, In vitro MIC Screening

Food & Safety Analysis

  • Analysis of Food as & Agricultural products as per FSSA (Food Safety and Standards Act).
  • Microbiological analysis,   detection  and
    identification of pathogens.
  • Proximate analysis and nutritional labeling of food
  • Shelf life estimation of packed food.
  • Fatty acids composition and trans-fat content.
  • Spices & Condiments analysis

 

Oniosome Healthcare Private Limited

Water Testing

  • Packaged Drinking Water, Drinking Water, Portable & Domestic Analysis
  • Organic and Inorganic Constituent Profile
  • Total Organic Carbon (TOC analysis)
  • Microbiological Quality of Water
  • Water for swimming pools
  • Water for paper and pulp industry
  • Sea water and brines as per customer specifications

Cosmetics

  • Testing as per Bureau of Indian Standards (BIS)
  • Safety tests like heavy metals in cosmetics, banned colors and banned chemicals.
  • Microbiology testing for microbial counts and pathogens
  • Estimation of active ingredients
  • Functional tests like viscosity, spread-ability, scratch test, pay-off test
  • Skin irritation studies
  • Stability studies for shelf life estimation
  • Complaints investigation and troubleshooting

Dairy Products

  • Raw Milk Testing: Protein profile, antibiotics profile, casein and butterfat profile, free fatty acid, pesticide profile.
  • Pasteurized milk testing services: Protein profile, antibiotics profile, casein and butterfat profile and total viable count.

Oniosome Healthcare Private Limited Industrial Training

  • Instrumental Training: Exposure to analytical instruments such   as  HPLC,  UV-Vis
    spectrophotometer, etc. as well as formulation equipment including electrospinner, lyophilizer, etc.
  • Summer Training: Industrial training provided for UG/PG students of Pharmaceutical, Biotechnology, Microbiology and dietetics regime.
  • IPR Training: Introduction to IPR fundamentals, operation of IPR tools and literature mining.
  • QA/QC Training for UG/PG/Ph.D students

Accreditations

We are a DSIR certified organization; with our own Laboratories and partner Laboratories being subjected to the Rigorous and Stringent Standards & Benchmarks.

Please feel free to contact us with any question or comments regarding our services and product.

Contact Us:

Oniosome Healthcare Pvt. Ltd.
Plot: F-103, Industrial Area, Phase 7, SAS Nagar, Mohali —
160055

Tel: +91-9041601909, 9781859505
Email: [email protected],

[email protected]

Website: www.oniosome.com

Kindly send all queries related to dossier, formulation, analytical, validation and other technical services as well as related to training programs at email address provided above.

Oniosome Healthcare Private Limited

ABOUT US

  • Oniosome Health Care (p) Ltd. was established by a group of pharmaceutical scientist in the year 2010, at Mohali.
  • The organization was set up with a inputs from industry representatives, Scientists and renowned academicians with a vision to make advancements in the field of formulation development and Analytical Testing.
  • Target of organization is to develop innovative drug products & delivery systems, Technology transfer and to fulfill all analytical testing requirements of all pharmaceutical and API industry.
  • Projects in association with various reputed organizations: BIRAC/SBIRI/DBT/DST, Punjab
    University, NRDC, IMTECH, NIPER, ICT, Mumbai, IIT etc.
  • Product Pipeline
  • Working model of Oniosome healthcare Pvt. Ltd.

Oniosome Healthcare Private Limited

RESEARCH AND ACADEMIC SUPPORT — PHARMA,
BIOTECH & ALLIED SECTORS

  • Enriching & Facilitating Project and Research work pertaining to PG/Ph.D level — facilities of our organization for carrying out their research work and this is at concessional rates for Research Scholar, Lab facilities with our expert to the Research Scholar to Complete their research projects pertaining to their research work during masters and Ph.D degrees/Industrial Projects.
  • Scientific and Industrial, instrumental training for UG/PG/Ph.D Level.
  • Collaborative Projects with Funding Agency &
  • Assistance in           Placement,     jointly      organizing
    Conference, Seminars and Symposiums.

INDUSTRIAL SUPPORT

Formulation Research & Development

  • Conventional & Novel dosage form development: Tablet (Immediate Release, Sustained Release, Multilayered, FDT, Orodispersible, etc.); Capsule (SR), Creams, Gel, Lotion, Ointment, Patch, eye drop Nanoparticle, Liposome, Nanofiber Patch, etc.
  • Formulation Equipment: Tablet punching machine, Spray dryer, FBD, Rota evaporator, Homogenizer, stirrer, Electrospinner, Lyophilizer etc.
  • In-vitro Studies:       All        IPQC          parameter,
    Dissolution/permeation studies, Stability studies (40°C/75% RH; 25°C/60% RH; short term, long term and accelerated).
  • Technology Transfer, Reverse Engineering of existing products.
  • Regulatory Support: IPR, Copyrights, Trademarks, Dossier
  • Act as an expert consultancy for all stages of product development, scale-up, manufacturing, medical, science-based marketing.
  • Intellectual property support to identify potential drugs & strategic delivery system for development

Oniosome Healthcare Private Limited Herbal Testing

  • Extraction, isolation, phytochemical screening,
  • Total phenolic assay, Determination of steroid,
  • Heavy metals analysis, Antioxidant analysis.
  • Essential oil analysis, Quantitative analysis of phytoconstituents,
  • Chromatographic fingerprinting
  • Development of herbal formulation.

Analytical Research & Services

Products Tested as per USP, BP, EP, IP Methods and Customers

Requirements.

  • Preformulation/Physical chemistry Parameter: Solubility, Stability, Melting point, Refractive index, Partition coefficient, Dissociation constant, LOD, viscosity, ash value determination, content uniformity, acid value, peroxide value, optical rotation, etc.
  • Analytical method development & validation
  • Uniformity of content, Assay, RS analysis of API and Formulation.
  • Crystal geometry and polymorphism analysis
  • Thermal Analysis
  • Heavy metals analysis & Element analysis
  • Impurity quantification
  • BET surface area & average porosity analysis
  • Particle characterization with D10, D50 & D90 value
  • Residual solvent analysis
  • Stability Studies: Short term, long term,
    Accelerated Stability Studies as per ICH guideline (40°C/75% RH; 25°C/60% RH)

List of Test Parameters: Pharmaceuticals

1. HPLC

Parameter

Instrument

Run time of
injection

Charges for
1 molecule

Charges:
Combination of
two molecule

Charges:
Combination of
Three molecule

Identification of

HPLC-UV

0-30min.

500

800

1000.

API/Raw

HPLC-PDA

0-30min.

500

800

1000

material/Finished

HPLC-RI

0-30min.

600

900

1000

product/RS

HPLC-

0-30min.

600

900

1000

 

Fluorescence

 

 

 

 

Assay of API/Raw

HPLC-UV

0-30min.

500

800

1200

material/Finished

HPLC-PDA

0-30min.

500

800

1200

product/RS

HPLC-RI

0-30min.

600

900

1400

Single point
determination

HPLC-
Fluorescence

0-30min.

1000

1000

1500

 

For extra 30min. Per injection would be charges as per above rates of each injection

Preparation of

HPLC-UV

0-30min.

3000

4800

6000

Linearity curve

HPLC-PDA

0-30min.

3000

4800

6000

(Concentration

HPLC-RI

0-30min.

3600

5400

6000

points =6)

HPLC-

0-30min.

3600

5400

6000

 

Fluorescence

 

 

 

 

 

For extra 30min. Per injection would be charges as per above rates of each injection

Uniformity of

HPLC-UV

0-30min.

700

1200

1500

content

HPLC-PDA

0-30min. •

700

1200

1500

 

HPLC-RI

0-30min.

800

1500

1800

 

HPLC-

0-30min.

900

1600

2000

 

Fluorescence

 

 

 

 

 

For extra 30min. Per injection would be charges as per above rates of each injection

 

 

 

 

 

 

Dissolution (Single

HPLC-UV

0-30min.

500

800

1000

point)

HPLC-PDA

0-30min.

500

800

1000

Fran

HPLC-RI

0-30min.

600

900

1000

diffusion(Single
point)

HPLC-
Fluorescence

0-30min.

600

900

1000

 

For extra 30min. Per injection would be charges as per above rates of each injection

·        HPLC method development &validation as per ICH guideline (Depend on the method / Case to Case

variations)

·        Impurity should be provided by Sponcer

·        Dissolution and Franz diffusion only include charges for analysis only

·        Forced Degradation as per ICH guideline quotation shall be offer upon request

2. GC

Parameter

Instrument

Run time of
injection

Charges:
API/Raw
material/Residual
solvent
/RS/Volatile
solvent

Charges:
Residual solvent
/RS/Volatile
solvent upto 4

Charges: More
than 4
API/Raw
material/Residual
solvent
/RS/Volatile
solvent

Identification and
Assay of API/Raw
material/Residual
solvent /RSNolatile
solvent

GC

0-30min.

1000

2000

700per solvent

GCMS

0-30min.

3500

4000

2000 per solvent

GCMS-HS

0-30min.

3500

5000

3000 per solvent

 

 

 

 

 

Benzene & Related
substance

GC

0-30min.

1500

-

-

Nitrogen Content
Assay

GC

0-30min.

1500

-

-

Ethanol content

GC

0-30min.

2000

,               -

-

·        For extra 30min. Per injection would be charges as per above rates of each injection

·        Method development &validation as per ICH guideline (Depend on the method / Case to Case variations)

·        Forced Degradation as per ICH guideline quotation shall be offer upon request

 

3. MASS and LCMS

Parameter

Instrument

Run time of
injection

Charges: 1
API/Raw
material /RS/

Charges:
API/Raw
material /RS upto
2

Charges: More
than 2
API/Raw
material /RS

Identification and
Assay of API/Raw
material/Residual
solvent /RS/Volatile
solvent

MASS
(+ &- mode)

 

2500

-

-

MS-MS

0-60min.

5000 per hour of
Instrument time

-

-

LCMS

0-30min.

3500

5000

1000 per solvent

LCMS-MS

0-30min.

Quotation upon request

·        For extra 30min. Per injection would be charges as per above rates of each injection

·        Method development &validation as per ICH guideline (Depend on the method / Case to Case variations)

·        Forced Degradation as per ICH guideline quotation shall be offer upon request

4. TLC & HPTLC

Parameter

Instrument

Run time of
injection

Charges: 1
AP1/Raw
material /RS/

Charges:
API/Raw material
/RS upto 2

Charges: More
than 2
API/Raw
material /RS

Identification and
Assay of API/Raw
material/RS
Single point
determination

TLC

-

500

750

250 per
compound

HPTLC

0-30min.

2500

4000

1500 per
compound

Preparative
HPLC/Semi-
Preparative HPLC

0-60min.

4000 per hr

-

-

·        For extra 30min. Per injection would be charges as per above rates of each injection

·        Method development &validation as per ICH guideline (Depend on the method / Case to Case variations)

·        Linearity curve preparation extra cost would be shared upon request

·        Forced Degradation as per ICH guideline quotation shall be offer upon request

 

S.No.

Name of Instrument

Charges

5

Instrumentation

 

5.1

Scanning & identification by UV/VIS spectrophotometer

250

5.2

Assay by UV( blank+ standard sample)

1000

5.3

Uniformity of content by UV

1500

5.4

Dissolution study as per time point (8pt.)

3000

5.5

In vitro permeation study (Franz diffusion study)

2500

5.6

Method development and Validation as per ICH guideline

Case to Case Variation

5.7

Scanning &Identification by F.T.I.R

200

5.8

Identification by Raman Spectroscopy

5000

5.9

Identification by Circular Dichroism

2500

5.10

Identification OF specific rotation by Polarimeter

1000

5.11

Identification OF specific rotation by refractive index

300

5.12

Identification by Florescence Spectrophotometer

Rs. 2000 / sample For Plate
reader Rs. 4000per plate

5.13

NMR Spectrometer 1H,13C,15N,31P (With solvent CDCI3)

2500

5.14

NMR Spectrometer 1H,13C,15N,31P (With solvent DMSO, CDC13)

3000

5.15

X ray Diffractometer XRD-(Powder)*, 2 theta (10-60 degree)

2000

5.16

X ray Fluorescence XRF

2500

 

 

 

6.

Titration

 

6.1

Aqueous     titration     /   Potentiometer  titration     /Titanium chloride  titration /Argentometric titration/ Non aqueous titration

400/Each

6.2

Assay by Chemically

400

6.3

Ceric ammonium Suphate/chloride

400

6.4

Uniformity of content by Titrimetry

600

 

 

 

7

Thermogram

 

7.1

Loss of Drying/MP-BP/Moisture content

500

7.2

DSC (Room temperature to 450°C)

2500

7.3

DSC (-40°C to 450°C)

4000

7.4

TGA

2500

7.5

Vacuum LOD

300

7.6

Loss on ignition

300

 

 

 

8.   

Microscopy

 

8.1

Optical Microscopy

500

8.2

Particle Size by Sieve

400

8.3

HOT stage microscopy/Polarizing microscope (Identification of shape and Determination of size, D10, D50 and D90 value)

5000

8.4

Mastersizer analysis of API using dry method/Wet Method

1500

8.5

Nano Particle size analysis

1500

8.6

Nano Particle size analysis with Zeta Potential

2500

8.7

Confocal laser scanning microscope*

Rs4000/-sample 2000/-per
slide Fixed sample

8.8

SEM (Scanning Electron Microscopy)

4000

8.9

FESEM

6000

8.10

HRTEM

5000

8.11

CRY() TEM

30000

9.   

Element analysis

 

9.1

Atomic Absorption Spectrometer

(As, Ba,Cd ,Cr ,Hg, Mg, Ni, Pb, Sb, Se, etc...)

Rs 500 per element

9.2

Elemental Analysis * (C,H,N,S)

5000

9.3

Elemental Analysis * (0,F)

5000

9.4

Single element per sample (ICPMS)

1500/-

9.5

Method development and validation

50,0000 /-

9.6

Inorganic elements by ICP-OES

1000

9.7

Method development & validation

3,00,000/

 

 

 

10

In vitro cell line study

 

10.1

MTT assay & Cellular Uptake Assay

Depend upon the no. and cell line

10.2

Apoptosis assay

'

Depend upon the no. and cell line

 

 

 

11

Ultracentrifuge

2000

12

Dissolution/ Franz diffusion Without analysis upto 8hr.

1500

13

Steroid assay and Enzyme Assay

500 each

14

Identification by Chemically

200

15

Viscosity ( Brookfield viscometer)

400

16

Rheometer

1000

17

Texture analyzer

4000

18

Electrospinner for preparation of Nanofiber

8000 per hr.

19

Spray dryer

5000 per hr.

20

Freeze drying and Lyophilisation

3500 per 24hr per 100m1

21

Degree of polymerization

500

22

Ether soluble substance

500

23

Boiling range /distilling range

200

24

Clarity and Color of solution

300

25

Congealing range or temperature

300

26

Density

200

27

Disintegration time/ Friability test /Hardness/Content uniformity- tab/caps/ Bulk Density and Tapped density, Average net content of capsule/injection /tubes

200/Each

28

Carbohydrate/ Fat/ Calories /Energy/ Protein

450/Each

29

Fiber

1500

30

Freezing Point

200

31

Fatty acid Composition (by Gas Chromatography )

2500

32

Paper Chromatography

600

33

Steroids identification

400

34

Nitrogen Content using Kjeldahl method

1500

35

Pyrogen Testing /Abnormal Testing

5000/Each

36

Peroxide Value, Hydroxyl Value, Iodine Value, Saponification Value, K-Value, PH Value

500/Each

37

Solubility test as per IP/BP/USP

500

38

Sulphated ash

400

39

Water Content by KF Titrator

200

40

Weight per ml/ Relative density

200

41

Suspended solids

400

42

Pesticide Group testing

8000

43

Pathogen testing in water (Four Pathogen )

400

44

TVC/ TFC

500/Each

45

Sterility test

1500

46

BET

1500

47

BET Surface Area Analyser

10000

48

Porosity meter

15000

49

Water Analysis

 

 

 

 

49.1

Complete testing of Raw Water /Drinking Water /R.O Water / Bore well water / potable Water as Per IS 10500 (with Radio activity ,Pesticide and Micro &Chemicals)

2000

49.2

Raw Water /Drinking Water /R.O. Water /Bore Well Water (Without P.C.B,P.A.H,)as per IS 10500

12000

49.3

Drinking Water (Essential Test ) as per IS; 10500

3500

49.4

Raw Water /Drinking Water /R.O.Water /Bore Well Water (Without radio)

10000

49.5

Purified Water I.P. 2018

5000

49.6

Effluent Water Compulsory Test (Without Bioassay )The Environment (Protection )Rules , 1986

4000

49.7

Pesticides in water ARE : 1453 (Required qty. of Sample 4 Lts )

8000

 

 

 

50

Microbiological testing

 

50.1

Anti-Microbial, Testing (Identification) E.Coli, Pseudomonas, Bacillus etc.

1000

50.2

Anti-Microbial, Testing (Determination of MIC) E.Coli, Pseudomonas, Bacillus etc.

 

50.3

Anti-Fungal Testing (Identification)

1000

50.4

Anti-Oxidant Testing (DPPH assay)

 

 

 

 

51

Stability study (As per ICHGuideline)

15000

51.1

1) 25 °C ± 2 °C/60% RH ± 5% RH

2) 30 °C ± 2 °C/65% RH ± 5% RH or 30 °C ± 2 °C/75% RH ± 5%

3) 40°C / 75% ( 6 months)

4) Photo stability study (7 days, 15 days and 20 days)

Stability studies as per
regulatory Requirements

List of Test Parameters: Ayurvedic/Homeopathic Medicine

S.N.

Sample Name

Test Parameters

Cost in INR

1

Mother
Tinctures

Determination of Alcohol Content in %

1500

pH value

150

Specific gravity

350

Total Solids in %

500

X — max by UV Spectrophotometer

Method & Std.
Required

Identification of Active Principle present in the Drug (By
TLC) (Please specify the drug name)

700 each content

2

Potencies/
Dilution

Determination of Alcohol Content in %

1500

Absence of Fusel Oil

Method Required

Absence of aldehydes & ketones

Method Required

Drug content up to 3x Level

700 per potency

3

Biochemic
Tablet

Determination of Disintegration / Dissolution time

350

Test for lactose by HPLC

2500

Percentage of Ash value w/w

500

Identification of Drugs up to 3x

700 per potency

4

Ointments

Determination of Consistency & Homogenicity

Method Required

Base material

Method Required

Drug Content (Please specify the drug name)

Required Standard

Identification of claimed drug by TLC (Please specify the drug
name)

700 each content

'    5

Hair Oil

Determination of Test for base oil

Method required

Identification of drug by TLC (Please specify the drug name)

700 each content

Determination of Acid value

500

Determination of Iodine value

500

Determination of Saponification value

500

 

List of Formulation: Cosmetic

S. N.

Test Parameters

Cost in INR

 

1

Baby oils and lotions

 

 

2

Face scrub, Fairness creams, Bleach

 

 

3

Shampoos and conditioners, Soaps,
Shaving creams

 

 

4

Hair colours and dyes

 

 

5

Hair gel

 

 

6

Henna and Mehndi

 

 

7

Kajal, Lipsticks, Lotion, Mascara

 

 

8

Nail polish,

 

 

9

Perfumes and deodorants, Powders

 

 

10

Sunscreens, Tooth paste

 

 

 

  • Analysis of raw materials and active ingredients
  • Cosmetic testing as per buyer or manufacturer specifications
  • Complaints investigation and troubleshooting
  • Development of cosmetic testing protocols for private label products
  • Estimation of active ingredients
  • Microbiology testing for microbial counts and pathogens
  • Safety tests like heavy metals in cosmetics, banned colours and banned chemicals
  • Functional tests like viscosity, spread-ability, scratch test, pay-off testStability studies for shelf life
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