Risk Management: A Brock Hallmark.
Brock builds Risk Management into every project we perform because we know that risk is inherent to all projects undertaken in highly regulated industries. We have established a comprehensive definition of risk, and an effective methodology for managing risk for our clients. Risk factors and associating methods for controlling them are identified as:
 - Risks to Project Completion
 - Risks to Project Success
 - Risks to Project Quality
 - Risks to Project Approval






Overview | Automation Engineering | MES | Manufacturing IT | Simulation & Testing | CSV
Computer System Validation

Brock's pharmaceutical experience includes successful completion of 500+ projects involving the functions of commissioning, qualification, and computer system validation. Qualification methods are based on GAMP 4 and ISPE (International Society for Pharmaceutical Engineering) standards, and include compliance with 21 CFR Parts 11, 210, 211, and 820.

CSV is prescribed for: Benefits include:
  • Qualifying plant-floor automation
  • Integrating automation and CSV
  • Simplifying equipment C&Q
  • Facilitating project cycle control
  • Expedited capital projects
  • Assured CSV compliance
  • Increased speed to market
  • Maximized system operability

For more information please contact our Pharmaceutical Process Division.