Medisca Medisca
     United States   
 
Thursday, December 04, 2008
 
   
 
Quality Control
 

All of Medisca’s Active Pharmaceutical Ingredients (APIs) and Fine Chemicals are manufactured in FDA registered and inspected factories that conform to current cGMPs.

We adhere to Current Good Manufacturing Practices (cGMP) and our Quality Control Department tests all chemicals to meet the latest requirements of the United States Pharmacopeia/Natural Formulary (USP/NF) and British Pharmacopeia (BP). We guarantee the products you receive are of the highest quality.

At Medisca, Excellence is our Standard!

To further meet your needs, Certificates of Analysis, Material Safety Data Sheets (MSDS), and Technical Specifications for all APIs and Fine Chemicals are available both online and on request.

We offer a full range of testing from independent outside FDA inspected laboratories.

Quality Testing

  • Chromatographic Purity
  • Color of Solution
  • Completeness of Solution
  • GC Assay, Heavy Metals
  • Heavy Metals II
  • Infrared Absorption
  • Loss on Drying
  • Loss on Ignition
  • Melting Range
  • Ordinary Impurities
  • Organic Volatile Impurities
  • Particle Size
  • pH Determination
  • Related Compounds
  • Residual Solvents
  • Residue on Ignition
  • Specific Rotation
  • Thin Layer Chromatography (TLC)
  • Titration
  • Ultraviolet Absorption
  • Viscosity Test
  • Water Method

Quality Testing on Demand

  • Bacterial ID (per identified organism)
  • Endotoxin
  • Fungal Testing
  • Species Identification
  • Sterility, ppt Test (Precipitate Test)
  • Rf Match

 


Privacy Policy  |  Terms & Conditions  |  Website Use Agreement Copyright ©1986-2008 Medisca Inc. All rights reserved