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Vitacorp International

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Review C of A and MSDS. Samples tested on Mass Spec & HPLC ... Capsule, tablet, chewable/sublingual, soft gel, liquid or powder for best delivery method ... – PowerPoint PPT presentation

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Title: Vitacorp International


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  • Manufacturing
  • and
  • Quality Control Processes

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Vitacorp Formulation Process
  • Health condition Selection
  • Best Ingredients for health condition
  • Contraindications with medications
  • FDA or other warnings

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Sourcing Process
  • Highest quality raw material available
  • Studies/Research/Clinical/Validation
  • Review C of A and MSDS
  • Samples tested on Mass Spec HPLC
  • Visual, pH, density and solubility testing
  • Near Infrared blueprint validation

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Sourcing Process
  • Capsule, tablet, chewable/sublingual, soft gel,
    liquid or powder for best delivery method
  • Best bioavailable/absorption delivery method
  • Packaging and shelf stability
  • Master formula documentation

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Quality ControlQuality Assurance Division
  • NIR/HPLC/Mass Spec/Microbiological

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HPLCHigh Pressure Liquid Chromatography
  • Quantitative ingredient analysis
  • Elemental potency and activity
  • Label claim compliance
  • Source assurance method

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Mass Spectrometer
  • Molecular density validation
  • Occurance of elements and compounds on the
    periodic chart
  • Mostly used for mineral content ID
  • Capable of measuring to 1-ppt
  • Also used for urinary spectrographic analysis

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NIRNear Infrared Spectrometer
  • Qualitative ingredient analysis
  • Identifies 450 viewpoints within a compound that
    is generated on a graph
  • Blueprint Validation
  • Tests before and after completion of a product
  • Stores the info for future comparison

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Microbiological Lab
  • Test for contamination and impurities
  • Yeast Mold
  • Coliforms
  • E.coli
  • Staphylococci
  • Aerobic Plate Counts

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Manufacturing and QC
  • GMP/SOP Dedication to quality consistency
  • All ingredients must match blueprint analysis
    on the NIR
  • Stored in temp/climate controlled area
  • Particle sizing
  • Microbiology/QC/QA

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Blending
  • Each ingredient is pre-measured into pre-blend
    containers
  • QC verifies all pre-blend weights
  • Pre-blend is put into the V-Blender system for
    thorough mixing Nitrogen flushing
  • Batch then moves through QC verification to
    tablet, capsule or powder dept.

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Liquid Blending
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Tablating
  • Compression is set on the tablet press
  • Powder is compressed into specific weight
    variations
  • QC weight verified in 10 minute intervals
  • Batch moves from tablating to coating for
    finishing

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Coating
  • QC Validation
  • Tablets are coated in coating pan
  • Drying time
  • Stored in polyethylene lined boxes awaiting QC
    approval and package scheduling

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Capsules
  • Machine is set up for required fill weight and
    capsule specifications
  • QC weight verified in 10 minute intervals
  • Capsules are sent for inspection and polishing

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Capsule Inspection
  • Completed capsules are put into the polisher to
    remove dust and any broken capsules
  • Entire batch is visually inspected and QC
    verified for weight, closure and appearance
  • Capsules are stored in temp/climate controlled
    area until ready to bottle

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Packaging
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Laser Counting
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Digital Cot toner
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Capping Station
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Torque Station
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Foil Induction Sealer
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Labeling Station
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Neck Bandar
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Neck Body Shrink Tunnel
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Powder Filling Station
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