In the competitive world of pharmaceutical and biotech research and development, regulations and guidelines, such as FDA 21 CFR Part 11, cGxP, GAMP and DEA guidelines, as well as internal standards require proven solutions and tools that meet challenging regulatory compliance standards. Companies that do not meet these standards or requirements can see negative impacts to their businesses and can be subject to fines or other penalties (e.g., even having their operation shut down).

Honeywell has improved our product offerings with the addition of features and functionality specifically targeted at meeting these needs. For examples, Pro-Watch has features that specifically address everything from audit logs to digital signatures and multiple signature approvals. Investing in Honeywell solutions provides the double value of improving both business practices and auditing processes. In addition to supporting the requirements, Honeywell offers a fully integrated solution, so users can not only meet requirements, but also have video proof of what has happened.