Weist EDV | complete IT-Solutions from one source

Our estbalished SDLC

Weist EDV uses for its Development of Software in the GxP fields a numerous established SDLC (System Development LifeCycle) as a Developmentlifecycle.
We assign all Validation- and Developmentjobs to our SDLC. Within the liefcycle Weist EDV makes several methodical test of the given specifications, design and the development itself.

Softwaredevelopment for the pharmaceutical and medical industry based upon:

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	Home Portfolio Postvalidation

You faced with the challengue of validating your newly developed software against the GMP-field.

We can help you through our validation experience and take care of the post validation of your product.

Weist EDV can certify that your software has complied with all quality characteristics needed for Standards GAMP 5 and 21 CFR Part 11.

We support you with creating all necessary GxP Compliancy Documentation. The documentation holds all effeciency and many validation rules in a clear simple format.

We take into consideration the requirements for FDA as well as as the Code of Ferderal Regulations 21 Part 11.


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	GxP (Good x Practice)

Weist EDV has a long time experience in Softwarevalidation for the pharmaceutical industry as like as for the medical fields.

Our business activities include also the fast and precise creation of your User- and Inventory Specifications.

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