Honour Life Sciences offering entire gamut of analytical studies required for crop protection agents and industrial chemicals development to meet the global regulatory requirement as per OECD, EEC, ICH, ABNT NBR, CIPAC, SANCO, OPPTS (OCSPP), EPA, WHO, FAO, CIB_RC, BIS, EU and other guidelines to enable US-EPA, EU, Brazilian, Mexican, Australian, Canadian, Indian CIB registration and other global submissions.
- Active Ingredient
- Relevant Impurity Identification and Quantification
- Analytical Test Report (ATR) – Characterization of Test Substance
- Container content compatibility
- Method Development and Validation
- Residue & Persistence Studies (Soil, Water & Plant)
- Five Batch Analysis
- Pre-screening of 5-batches for impurities including 3D screening
- Impurity identification and structure elucidation in consultation with the sponsor
- Isolation/synthesis of impurities required for 5-batch analysis
- GLP analysis of 5-batches using validated analytical methods for active ingredient content and impurities
- Characterization of 5 commercial batches along with reference standards by UV, IR, NMR, LC-MS/MS and/or GC-MS as applicable
- Storage Stability (0°C, 54 ± 2°C, Ambient conditions, multilocation, etc.)
- Accelerated
- Real time
- Multi-location
- Long term storage stability with corrosion characteristics
- Environmental Fate Studies
- Adsorption / desorption study on soil
- Rate of degradation on soil (aerobic and anaerobic) and metabolism
- Rate of degradation on sediments and metabolism
- Hydrolysis and Photolysis in water
- High Temperature hydrolysis
- Soil microorganisms: Nitrogen transformation test
- Soil microorganisms: Carbon transformation test
- Mobility in soil
- Activated Sludge/Microbial Activity
- Aerobic/Anaerobic Degradation
- Soil, Plant and Animal Metabolism
- Soil Adsorption and Desorption
- Hydrolysis and Photolysis
- Leaching
- Physical and Chemical Properties (Technical / Formulations)
- Physical State, Color & Odour
- Melting Point/Boiling point/Freezing point
- Solubility in Water / Organic Solvents
- UV-Visible absorption spectra
- Dissociation Constant
- pH/Acidity/Alkalinity
- Vapour Pressure
- Spontaneity of Dispersion
- Chemical incompatibility (Oxidation/Reduction)
- Container Content Compatibility
- Corrosively/Corrosiveness
- Suspensibility
- Photolysis characteristics
- Stability to metals, Metal Ions & Elevated Temperature
- Emulsion Stability
- Surface Tension
- Moisture Content
- Pourability
- Suspensibility
- Persistence Foam
- Weight loss on heating
- Residue on Ignition
- Sieve Analysis
- Density/Specific Gravity
- Partition Coefficient
- Viscosity
- Flammability
- Solution Stability
- Molar Absorption Coefficient
- Explodability
Honour Life Sciences offering comprehensive range of analytical testing services in line with the regulatory requirements of DCGI, USFDA, TGA-Australia, and Health Canada (HC) to Pharmaceuticals, Bio Pharma
Analytical-Instrumental
- Dissolution Studies
- Raw Material and Excipient Analysis
- Method Development and Validation
- Particle Size Distribution Determination
- Surface Area Analysis
- Pharmacopeia Compendial Testing
- Solid State Characterization
- Stability Studies
- Extractable and Leachable Studies
- USP & ICH Impurity Profile
- Residual solvents/impurities
- Process impurities
- Degradation products
- Trace metals
- Elemental analysis
- Structure elucidation
- Forced degradation studies
Analytical-Microbiology
- Clean Room Environmental Monitoring
- Hand Sanitizer /Disinfectant Efficacy Evaluation
- Microbial Kill Rate Studies
- Bacterial Endotoxin Test (BET by Gel Clot & Kinetic Methods)
- Sterility Testing
- Microbial Limit Test (MLT)
- Antimicrobial Effectiveness Test (AET)
- Preservative Efficacy Test in cosmetics (PET)
- Water System Validations
At Honour Life Sciences, we are offering analytical testing services to medical device manufactures as per ISO 10993 to submit across the globe.
- Extractable and Leachable Studies (ISO10993, Parts 17 and 18)
- Chemical Characterization (ISO10993, Part 18)
- Phthalate Estimation
- CMR/ED Estimation
- Structure Activity Relationship
- CFR Monograph Testing
Our expertise synthetic chemistry team Synthesis, Isolate, Identify and Characterize any type of impurities/intermediates based on the sponsor/customer requirements.
Custom made Impurities/intermediates are characterised by using NMR, LSMS, GCMS, IR etc. and supplied to clients.
We supply following type of molecules based on client requirements.
- Impurities
- Intermediates
- Standards
- Deteriorated standards