Our GMP Deviation Management software helps companies track all deviations, errors and other recordable events including follow-up corrective and preventive actions to be taken.
It enables engineers and experts to investigate and determine root causes of deviations. It is compliant with industry regulations, including Title 21 Code of Federal Regulations Part 11, Part 210 and 211.
GMP Deviation Management runs on Microsoft IIS and uses ASP.NET 2.0.

Price: 2.990 €
What is GMP?
GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration. These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective.
Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
In the long run, it is more expensive finding mistakes after they have been made than preventing them in the first place. GMP is designed to ensure that mistakes do not occur. Implementation of GMP is an investment in good quality medicines. This will improve the health of the individual patient and the community, as well as benefiting the pharmaceutical industry and health professionals.
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