Drug Formulation Procedures

The drug subjected to drug development undergo number of trials and are screened at different stages to produce a final potent drug for the treatment of various diseases. During this process different properties are checked to see whether the drug is non-toxic to living system and is therapeutic or not. Using suitable excipients and technological preparations the active substances are formulated into final dosage form. The final product is the Actual composition of preparation, manufacturing specification.

A detailed analysis of the industry structure of contract manufacturing, contract research and contract packaging has been conducted. Revenues are broken down by type of industry. Sales figures are estimated for the five-year period from 2013 through 2018. The United States is currently spending almost $250 billion a year for prescription drugs. If drugs were sold in a competitive market, without government-imposed patent monopolies, this might achieve savings up to $200 billion a year.

  • Types of coating and coating procedures
  • Sterile filtration, Aseptic filling
  • Lyophilized dosage forms
  • Development of parenteral dosage form
  • Validation process
  • Advanced formulation techniques
  • Developing a preparation of the drug
  • Formulation from plant sources
  • Rational vs. empirical approach to the formulation development
  • Chemical stability of drug in solid state and in solution
  • Drug absorption and permeability
  • Formulation development of peptides and proteins
  • Analytical methodologies in the formulation development

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