Comprehensive free webinars on 21st century approach to attaining quality objectives, statistical trending and increasing efficiency from Novatek International
Compliance has become a critical mission for many organizations.
The proliferation of regulations such as Title 21 of the US Code of Federal Regulations Part 11, cGMP, various international guidelines, as well as increased inspection from internal and external auditing agencies have impacted all areas of operations.
Problems associated with laboratory information management, documentation, reporting and personnel training are among those most commonly cited as objectionable during FDA inspections of pharmaceutical manufacturing facilities.
In today's competitive pharmaceutical market, Fortune 500 companies are constantly striving to reach higher levels of process maturity and compliance by adopting high-tech tools.
Novatek's process-based solutions have helped companies meet those objectives.
During these technical webinars, we will present you with a demonstration of Novatek's 21 CFR Part 11 compliant software solutions, the only specialised solutions in the modern pharmaceutical-IT marketplace.
Each webinar will be followed by a 30-minute discussion session featuring a highly respected expert in the field.
