formurex presentation
DESCRIPTION
TRANSCRIPT
- 1.
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- Welcome
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2.
- Formurex is a contract research organization that serves the pharmaceutical industry in drugformulation development .
- We also manufacture drug materials to supportPhase I clinical trialsunder GMP environment.
The Company & Values 3.
- Our Values
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- Quality
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- Professionalism
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- Respect
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- Innovation
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4.
- Mission Statement
- Our mission is to serve the pharmaceutical and biotech industry to advance medicine frombench to bedsideusing cutting edge technologies in drug formulation and delivery.
5.
- SERVICES
6. FormulationDevelopment AnalyticalServices GMPManufacturing Pre-Formulation StabilityStudies 7.
- Preformulation Services
8.
- Solubility Testing & Enhancement
- Permeation Testing & Enhancement
- Drug-Excipient Compatibility Studies
- Moisture Uptake / Hygroscopicity
- Density and Compressibility
- Surface Morphology and Particle Size Analysis
- Thermal Analysis
- Nano-sizing
9.
- Formulation Development
10.
- Direct compression
- Dry Granulation / Roller Compaction
- Spray Granulation
- Fluidized Bed Coating / Air-Suspension Coating
- High Shear Mixing / Granulation
- Multilayer Tableting
- Spray Drying
- Freeze Drying
- Extrusion & Spheronization
- Hot Melt Extrusion
Development of Oral Tablets, Capsules, Dry Powders 11. Direct Compression High Shear Mixing / Granulation 12. Dry Granulation / Roller Compaction Dry Granulation / Roller Compaction 13. Fluid Bed Processing: Granulation / Drying / Coating Spray Drying 14. Nano-Suspensions 15. Analytical Services 16.
- UV-VISSpectroscopy
- RP-HPLC
- SEC-HPLC
- Ion Exchange-HPLC
- Moisture content
- Loss on Drying
- pH measurement
- Density
- Viscosity
- Osmolarity
Routine QC Testing of Drugs and Pharmaceuticals 17.
- Single componentanalysis
- Multi-componentanalysis
- RP-HPLC and UV /PDA / RI /Fluorescenceanalysis
- Chiral separations
Analytical Method Development for Drugs and Pharmaceuticals 18.
- Accuracy
- Precision
- Specificity
- LOD
- LOQ
- Linearity Range
- Robustness
Analytical Method Validation for Drugs and Pharmaceuticals 19. Dissolution Testing & Method Development 20. Stability Services 21. Stability testing for APIs, and formulations at different T/H conditions as per ICH / FDA guidelines 22. GMP Manufacturing 23.
- Capacity:
- 3000-15000tablets / h
- 6000 capsules /day
24. Quality Management 25.
- Visit us at: www.formurex.com
Contact:[email_address] (510) 206-4667 26. Thanks!!