| | Commissioning, Engineering Design, Qualification /
Validation and Regulatory Affairs of the cGMP
Biopharmaceutical, Medical Devices, Pharmaceutical and
Food industries. NCS Pharmaceuticals employees have been
greatly involved with the commissioning and validation of
equipment, systems and entire facilities since the inception of
validation by the pharmaceutical industry. We utilize our
cGMP compliance and validation methodology which is
developed by NCS Pharmaceuticals to optimize the execution
of the commissioning and validation phases of a project. This
methodology allows us to generate a cost effective validation
program minimizes overall project execution time. Our
employees are highly qualified in the industry who are
continually trained in the latest developments in the field.
Download NCS Qualification Package/Profile
Download NCS Experience Document
NCS Pharmaceuticals provides validation services
independently or in conjunction with commissioning
operations in order to optimize project cost and time. NCS
Pharmaceuticals will deliver the services required to meet
your specific needs. NCS Pharmaceuticals offers the
following activities:
 | | Design Reviews
|
| | Validation Master Plans
|
| | Commissioning Plans
|
| | User Requirement Specifications (URS)
|
| | Functional Requirement Specifications (FRS)
|
| | Detailed Design Specifications (DDS)
|
| | Factory Acceptance Test (FAT)
|
| | Site Acceptance Test (SAT)
|
| | Commissioning Protocols
|
| | Installation Qualification (IQs) Protocols
|
| | Operational Qualification (OQs) Protocols
|
| | Performance Qualification (PQs) protocols
|
| | Cleaning/Sanitization Validation Protocols
|
| | Computerized Systems Validation
|
| | Standard Operating Procedures (SOPs)
|
| | Employee cGMP Training
|
| | Equipment History Files Analytical Methods Validation
|
| | Site Validation Execution Site
|
| | Commissioning Execution
|
| | Final Reports Scheduling/Estimating and Project Management
|
| | cGMP Auditing Services
|
|
