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SMB Group Inc. has a extensive expertise in:
  • The Pharmaceutical, Medical Devices and Biotech Industries
  • Equipment Design and Construction
  • Validation Master Plans
  • cGMP Training
  • GAMP 4 documentation
  • Qualification documentation and implementation
  • Developing Standard Operating Procedures
  • Development of User Requirement Specifications (URS)
  • Detailed Design Specifications (DDS)
  • Factory Acceptance Tests
  • Site Acceptance Tests
  • Pharmaceutical production and packaging
  • Pharmaceutical production environment and physical facilities
  • Operator and Maintenance personnel training
  • Project Management
  • Quality auditing.

This experience provides a competitive advantage over other validation providers. Few equipment suppliers employ personnel that offer the training and experience of the SMB Group. On the other hand, few professional providers can profess to possess an equally in-depth knowledge of equipment design and assembly as SMB does. Therein lies the competitive edge; SMB Group Inc. offers a wider range of services than the competition along with significant practical “hands on” experience both from our customers’ perspective as well as that of the regulatory agencies.

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