The ValSource Consulting Group offers high level consulting services in the areas
of CGMP compliance, validation and pharmaceutical technology. We also offer program
management for large-scale engineering, construction and validation projects.
ValSource philosophy holds that a true “life-cycle” approach is necessary to implement
and validate projects in full compliance with CGMP regulations. The successful project
involves the integration of function, structure and test considerations and requires the
efforts of diverse groups. ValSource Consulting Group can bring the entire team together
and will manage their activities to ensure a project validated in a timely manner and for
a reasonable cost.
Services are not limited to new projects. We can apply our experience to continuing
operations, as well. In all cases, or consultants are geared not merely toward uncovering
problems, but toward providing solutions.
Consulting services include:
-
Validation program
development
-
Validation master
planning
-
Computer system validation
planning
-
CGMP operational
audits
-
CGMP design
audits
-
Pharmaceutical technology
and equipment
-
CGMP recovery
plans
-
Process and facility troubleshooting
Program Management services include:
-
Estimating
-
Scheduling/tracking
-
Resource management,
including procurement and management of sub-contracts
-
Turnover, commissioning and
start-up
-
Consent decree management
ValSource Consulting Group can help you achieve the most direct and cost-effective route
to CGMP compliance.
For more information contact:
David Calvaresi
Phone: (610) 269-2808
FAX: (610) 269-4069
