|Lotus Notes is
a world standard for collaborative applications. It is
a robust platform for development and maintanance of efficient web
and intranet applications for business workflow. With advanced use
of e-mail and instant messaging Lotus Notes enables faster and more
efficient communication amongst employees within company as well
as with other company partners. Lotus Notes is a very adaptable
information framework for every company and can be used by
thousands of users on different continents.
Usage of Lotus Notes applications enables faster and more comfortable
work in modern business environment where time saving, cost
effectiveness and well-organized documentation are essential. The
highest degree of data security is ensured. Software sollutions for
workflow and decision support will be a great help for managers and
team leaders in company. Intuitive interfaces are fully adaptable to
methods already in use in client's environment and require little or no
time for learning new tools. Connection between employees, business
processes and data sources in company or on web is improved when
using Lotus Notes tools.
|- system analysis,
management and supervising, prototyping, advising
- application design, implementing and documenting
- software design
and programming (web and intranet)
|- software and hardware consulting|
Portal is intended
for distance education on the Internet. It is designed in
|Application is designed for
monitoring and controlling projects and their
supporting documentation. Project terminology is fully configurable. All
time based events and components of a project can be graphically
represented (the Gantt diagram).
Application is designed
in Lotus Notes 5. It is designed for monitoring
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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