This Seminar will focus on the forms of data generated and the associated challenges in the pharmaceutical/biopharmaceutical GMP regulated Quality Control laboratory environment and will examine the impact of the MHRA Guidance for Industry regarding the maintenance of GMP data integrity throughout its lifetime.
The views of industry and vendors of major laboratory systems / software used in the generation, storage and retrieval of data throughout its lifetime will be explored
to establish how the major laboratory system / software vendors are helping industry to come into / maintain compliance with the regulations. The use of the latest data handling technology and, going forward - cloud storage will be reviewed.
The seminar will be of interest to Laboratory Managers and Scientists, QA / IT Personnel and QPs working in these regulated areas.
The views of industry and vendors of major laboratory systems / software used in the generation, storage and retrieval of data throughout its lifetime will be explored
to establish how the major laboratory system / software vendors are helping industry to come into / maintain compliance with the regulations. The use of the latest data handling technology and, going forward - cloud storage will be reviewed.
The seminar will be of interest to Laboratory Managers and Scientists, QA / IT Personnel and QPs working in these regulated areas.
