Validation Services

Effective Validation must be planned from the beginning of the Project and integrated throughout each phase. We can enhance this effort by utilizing our Experience, Expertise, and Quality attitude.

A key to providing value in the Validation Phase is to supply our Clients with input regarding the extent of the Validation Requirements. Our goal is to meet the Regulatory requirements in a practical and economical manner.

Design Services

The Design Documents are the only link between the needs of the Client and what the Contractor builds. We understand our Clients' needs and create Design Documents that clearly communicate the requirements through well coordinated, thorough details. We focus on Attention to Detail. In Design or Validation this means integrating all applicable aspects of the project to create Documents that are accurate, coordinated and will enhance the Construction or Validation Execution Services.

Process Improvement Services

The Process Operations are the "Life Blood" of any Pharmaceutical Company. Trident Engineering believes that the implementation of methods to Baseline, Monitor, Improve, and Maintain these systems can have an extreme positive impact on Product Quality and System Performance.

Trident's Services integrate these methods with the FDA's initiative of a Risk Based Approach and the trend to Process Analytical Methods to improve the Operational Productivity and Regulatory Compliance aspects of the Pharmaceutical Manufacturing or Packaging Operations.