g-docs™ GLP

An extremely important part of GMP is the documentation of every aspect of the manufacturing process, support activities, and operations involved with drug and medical device manufacture. If the documentation showing how the product was made and tested (which includes full traceability) is not correct and in order, then the product does not meet the required specification.  Traditional methods for managing these documents and data are cumbersome and expensive and are not designed for users.  g-docs™ GMP manages documents in a compliant manner and gives users a good experience.

 

Click here> to see the GMP process video


 

 

g-docs™ GMP can help you manage the quality documentation, templates and workflows, versions and revisions, and full audit trail of all of your GMP documents. Functional modules like ValMan™ can help you manage  computer systems facility, cleaning and equipment validation, g-SOPs™ can control the document templates and published SOP’s, changes and deviation managed by g-change™ and g-dev™ respectively, and training records and training can be delivered using g-train™.

 

If you are managing requirements on a large computer systems project then g-tracker™ can be used to co-ordinate that process.

 

Finally PDF rendering is delivered by our partners at Adlib and digital signatures by CoSign™ and these are fully integrated into g-docs™.