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],
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 |
Charges for |
Charges: |
Charges: |
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 |
HPLC- |
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 |
HPLC- |
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 |
Charges: |
Charges: |
Charges: More |
Identification and |
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 |
GC |
0-30min. |
1500 |
- |
- |
Nitrogen Content |
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 |
Charges: 1 |
Charges: |
Charges: More |
Identification and |
MASS |
|
2500 |
- |
- |
MS-MS |
0-60min. |
5000 per hour of |
- |
- |
|
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 |
Charges: 1 |
Charges: |
Charges: More |
Identification and |
TLC |
- |
500 |
750 |
250 per |
HPTLC |
0-30min. |
2500 |
4000 |
1500 per |
|
Preparative |
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 |
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 |
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 |
List of Test Parameters: Ayurvedic/Homeopathic Medicine
S.N. |
Sample Name |
Test Parameters |
Cost in INR |
1 |
Mother |
Determination of Alcohol Content in % |
1500 |
pH value |
150 |
||
Specific gravity |
350 |
||
Total Solids in % |
500 |
||
X — max by UV Spectrophotometer |
Method & Std. |
||
Identification of Active Principle present in the Drug (By |
700 each content |
||
2 |
Potencies/ |
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 |
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 |
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, |
|
|
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