Risk Of Mix Up And Cross Contamination

Risk Of Mix Up And Cross Contamination

A Mix–Up may be defined as:

  • An unplanned combination of various compounds.
  • A mistake brought about wrongly identifying one material for another.

A mix-up can be caused by bad judgement or lack of attention to detail, i.e., human error. It can also occur though poor communication between personnel.

More specific causes that may give rise to a mix-up include:

  • The close proximity or location of similar items
  • Items having the same colour or combination of colours
  • Multiple products handled at the same time/packaging
  • Use of the same apparatus or equipment for multiple products
  • Improper storage of sterile and non-sterile products
  • Care not being taken during packaging and/or repackaging of products
  • Mistakes made when dispensing
  • No proper line clearance procedure
  • Unused labels or earlier production left in the production area
  • Improper documentation and labelling
  • No ID code on materials or products
  • Inadequate training of personnel
  • Failure of the processing equipment
  • Manual packaging and repacking
  • Inadequate control or procedures
  • Rejection of handling
  • Improper affixing of labels
  • Reprocessing
  • Vendor’s Location, for example the printer may be located some distance from the PC or device that sends the output to the printer. The wrong person may mistakenly use the wrong printout e.g., for labels.
  • Improper or lack of proper communication
  • Same personnel handling two machines or equipment at the same time
  • Lack of proper validation


Contamination happens when there is a presence of and impurity or impurities in the material either in pre-production, during production or after production procedures. Impurities can be chemical, biological or microbiological by nature.

Cross Contamination is defined as the contamination of the material before, during or after the production starts with another product material.

Contamination of products can be caused by:

  • Contaminated clothing/attire
  • Contaminated equipment
  • Contaminated or faulty HVAC system
  • People, e.g., carrying harmful bacteria
  • Contaminated Premises
  • Processing Operations
  • Utilities/Services

Risk of Cross-Contamination

The level of the risk depends on the contaminant type and the contaminated product. High risk arises with

  • Biological preparations with living organism
  • Cytotoxic agents (i.e., materials that are toxic to cells and are generally used for the treatment of malignant and other diseases. They are designed to destroy rapidly growing cancer cells, and have been shown to be mutagenic, carcinogenic and/or teratogenic, either in treatment doses or animal and bacterial assays.
  • Use of highly sensitizing materials
  • Manufacture and processing of hormones

Contaminants in products become very significant when they are:

  • Applied to an open wound
  • Given in large doses
  • Injected
  • Administered over a long period of time

There are very serious consequences from contaminated products, both for the company and the individual employees. Companies may:

  • Suffer from adverse publicity
  • Be given compulsory closure notice
  • Suffer a significant loss of profit
  • Be subject to increasing and regular audits by the regulatory board
  • Be required to issue a show cause letter
  • Have their license to operate/manufacture suspended or withdrawn
  • Be issued with a warning letter

In addition to the serious adverse effects that contamination issues may have on companies. Employees may also suffer personally, e.g.:

  • Be temporarily suspended to allow investigation of the contamination issue
  • Suffer loss of income during suspension
  • Be required to supply a show cause letter
  • Face legal penalty – a fine or term of imprisonment
  • Have their employment suspended for a prolonged period or,
  • Face termination of employment

Related Articles

Contaminants Caused By Humans And Methods Of Control

Contaminantes Causados Por Humanos Y Métodos de Control

La contaminación es un problema importante en la fabricación de productos estériles y uno de los mas importantes que controlar. Las salas blancas son necesarias para mantener un entorno siempre libre de contaminación, pero son zonas difíciles de mantener. La sala blanca también puede ser una fuente importante de contaminación de no mantenerse limpia y estéril en todo momento. Sin embargo, la principal fuente de contaminación son los humanos que trabajan con los productos.

Different Types Of Contamination, Causes And Prevention For Pharmaceutical Industry

Diferentes Tipos de Contaminación, sus Causas y su Prevención para la Industria Farmacéutica

La presencia de materiales no deseados como polvo y partículas durante la manufactura y transporte se llama contaminación. El término contaminante incluye cualquier materia no deseada que se encuentre en el producto. Estos contaminantes afectan la calidad del producto o del proceso.<

Preventing Cross Contamination In Pharmaceutical Production Process

Evitando la Contaminación Cruzada en Procesos de Producción Farmacéuticos

Existen diferentes maneras de evitar que ocurran casos de contaminación cruzada durante la producción de productos farmacéuticos. A continuación encontrarás una guía que te ayudará a minimizar las posibilidades de que esto ocurra entre tus productos.

© 2024 LFA Machines Oxford LTD. Todos los derechos reservados.