helping your
business with

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  • Preliminary & Conceptual Design Review
  • Validation Strategy Master Planning 
  • Validation Protocol Development & Execution
  • Computer System & Automation Validation

  • Utility & Equipment Validation
  • ERP System Validation
  • Commissioning Activities

Our proprietary methodologies optimize commissioning & validation phases to keep projects on schedule & under budget.

Areas we have successfully addressed include:

Let Vantage keep your line productivity and management of your systems and facilities simple and cost effective. Our cGMP engineering & technical staff has experience in regulatory validation back to inception of regulations in the 1970s – with several helping to develop them.

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scope development lines/site/enterprise/support systems/clients

team designation/gap identification

as is/to be

project capital budget

program roadmap/approach summary

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vendor recommendations

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detailed project lifecycle/approach for bid

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recommendation on IT & network solutions

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Vendor Selection URS/RFP/FS

documentation development

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engineering installation/testing

training

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project monitoring/consulting (PM support)

customer briefs.

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additional services

validation.

streamlined serialization.

packaging line efficiency.

We’ve been involved with the validation of equipment, systems and entire facilities since the inception of validation regulations in the mid 1970’s. Our executive team has an average of over twenty five years hands-on experience in the Life Science industry.

Vantage Consulting helps our customers examine the immediate cost benefits of product serialization and product tracking through their specific manufacturing and distribution processes.

At Vantage, we take a holistic view of the entire packaging line – treating it as a single entity. In doing so, with a keen focus on a standardized, seamless integration of each piece of equipment, we realize a significant increase in the OEE.