WHO Basic Training Modules on Good Manufacturing Practices (GMP) - Basic Principles of GMP: Module 1 (Part 14): Sterile Pharmaceutical Products
(2006; 62 pages)
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Sterile Production

Sanitation

  • Frequent, thorough cleaning of areas necessary

  • Written programme

  • Regular monitoring to detect resistant strains of microorganisms

  • Chemical disinfection

  • Monitoring of disinfectants and detergents

  • Dilutions

    - clean containers, stored for defined periods of time

    - Sterilized before use, when used in Grade A or B areas

A high level of cleanliness is required in clean areas. Frequent, thorough cleaning of areas necessary according to a written program should be done.

Regular monitoring to detect resistant strains of micro-organisms should be done. A program for chemical disinfection and corresponding records should be available. Manufacturers also have to monitor disinfectants and detergents for effectiveness.

Preparation of dilutions should be done in accordance with a program and SOP - and records should be available. Disinfectants should be kept in clean containers and stored only for defined periods of time. These should be sterilized before use, when used in Grade A or B areas

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Última actualización: le 3 mayo 2013