Contact
ValMan™
The ValMan™
module is used to manage the
creation, review, approval, correction, completion and archiving of your
VMP, SQ, DQ, IQ, OQ, PQ protocols and test plans.
The module also has a validation deviation management process for
tracking changes to protocols and unexpected results when executing
protocols.
Good Products has a database of some 15,000 validation template
documents covering manufacturing equipment, lab equipment, computerised
systems for BioPharma, Laboratory and Clinical organisations.
Your existing templates, responsibility matrix, protocol review
and approval document workflows can be configured quickly into this
module, or you can use our pre-configured process.
ValMan™ documents are stored on
g-docs™ and can easily integrate with the
g-SOPs™ module,
g-train™ (or your
LMS), Documents and deviation forms can be signed
in the digital environment using
CoSign® or your digital signatures
package.
For more information contact ValMan@goodproductsEU.com