A project that fails to meet approval of governing bodies who mandate
regulatory compliance requirements is not only a failure, but also a burden
that necessitates unnecessary backtracking and associating time and money
expenditures. Brock's proven Project Methodology and Computer System Validation
and Automated Systems experience combine to assure that regulatory compliance
is built into the design and development of the lifecycle process. With Brock,
conformity to compliance mandates such as 21 CFR Parts 11, 210, 211, and 820
is built into the development cycle, with no backtracking required.
For more information please contact the Pharmaceutical Process Division.
