Analytical Services

Experienced partner for physical, chemical, analytical and bioanalytical sample testing. Modern labs
support strict quality control testing of chemicals, generic drugs, new APIs,
biopharmaceuticals and phytocostinuents.
Incorrect or wrong analytical methods can routine batch release-related analytical services, stability testing, formulation development, and technology transfer are accessible under one. The development of Roburst and a transferrable analytical method is key to any technical experiment or study whether it is formulation R & D or preclinical or clinical sample analysis. High-quality data and rapid turnaround time are key in lead drug selection and life cycle management programs. Our aim is to design, develop and validate fast, robust, transferrable regulatory complaint analytical methods for your samples.
The complementary expertise of Re8 facilitates analytical testing for
  • Generic drugs
  • New APIs
  • Biopharmaceuticals e.g. mRNA, vaccines
  • Phytoconstituents
  • Chemical entities
Our strong network of state-of-the-art laboratories and skilled chemists are happy to support you with cost-effective analytical testing, contaminants identification, and preclinical/clinical-related bioanalysis. Other related services like bioanalytical testing, routine batch release-related analytical services, stability testing, formulation development, and technology transfer are accessible under one umbrella.

Overview of Testing

  • Raw material testing and release
  • Standardization of reference materials
  • In-vitro testing
  • Stability studies
  • Packaging interaction testing
  • Microbial testing
  • Method transfer
  • Physical testing
  • Mycotoxins testing
  • Contaminant testing
  • Dioxin or pollutant testing
  • GMO status testing
  • Pesticide residue testing
  • Allergen testing
  • 3-MCPD and glycidyl esters
  • Pyrrolizidine alkaloids (PAs) are naturally occurring toxins
  • Veterinary drug residues
  •  Biopharmaceutical testing
  • Residual solvent testing
  • Active pharmaceuticals ingredients
  • Pharmaceutical dosage forms
  • Liquid samples
  • Tissue sample
  • Plasma samples
  • Urine samples
  • Excipients
  • Finished products
  • Personal care products
  • Medical devices
  • Packaging materials
  • Extractable -leachable
  • Air
  • Flavors-fragrances
  • Water
  • Soil
  • Waste
  • Building materials
  • Microbiological
  • Heavy metals
  • Veterinary drug residues 
  • Active substances identification
  • Quantification Assay
  • Impurity profiling
  • Drug release
  • Residual solvents
  • Elemental impurities (heavy metals)
  • Titration / Water (by Karl-Fisher) 
  • pH
  • Conductivity
  • Total organic carbon
  • Viscosity
  • Density
  • Specific gravity
  •  Refractive index
  •  Water activity
  • Disintegration melting point
  • Particle size distribution (wet/dry)
  • Particulate matter
  • Particulate
  • Osmolality and osmolality
  • Flash point
  • Moisture determination/LoD
  • Spectroscopy
          – UV/Vis
          – FT-IR
          – Atomic absorption spectroscopy – flame/graphite
  • ICP-OES and ICP-MS
  • Chromatographic tests
          – TLC
          – HPLC/UPLC (with UV, PDA, FLD,
          – GC/HS (with TCD/FID/MS – Detectors)
          – Gas chromatography-mass spectrometry/mass spectrometry (GC-MS/MS)
          – High resolution-gas chromatography/mass spectrometry (HR-GC/MS)
  • Electron microscopy
          – Scanning
          – Transmission
  • AFM microscopy
  • Fluorescence microscopy
  • Optical Microscopy and image analysis
  • Electron microprobe analysis (EMPA)
  • X-Ray Diffraction (XRD)
  • Heavy metals
  • Allergens
  • Preservatives
  • UV filters
  • Formaldehyde content
  • Nitrosamines
  • Phthalates
  • Pesticides & preservatives
  • 1,4 dioxane
  • Glycol ether
  • Polycyclic aromatic hydrocarbons (PAHs)
  • Volatile organic compounds (VOCs)
  • Substances of very high concern (SVHC)
  • Endocrine disruptors
  • Phenols (NP, OP, NPEO, OPEO)
  • Absorbable organic halides (AOX)
  • Biodegradability
  • Sterility testing
  • Microbial contaminant identification
  • Antimicrobial effectiveness testing
  • Microbial challenge tests
  • Mycoplasma testing
  • Microbiological assessment of antibiotics
  • Bacterial endotoxins testing
  • Testing for packaging, medical gloves, rubbers
  • Antibacterial testing for contact lenses, personal care products
  • Non-viable particulate testing
  • Total plate count
  • Yeast and mold – identification
  • Pathogens – identification
You can benefit from our network of chemical testing laboratories which has compliance against GLP, GCP, and FDA or alternatively, you can opt for USP, EP, ICH, FDA and EMA or monographically testing requirements.

We also support routine and non-GLP analytics.
We provide services to companies worldwide, faster, flexible and customized.
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