Validation Services
Are you implementing a new system or responding to an FDA 483 Warning Letter?
Given the complexity of the product development process, postponing the upgrade of facilities, equipment and software applications are not surprising in the life sciences industry. However, due to the vast and ever-changing regulatory standards, it is critical to remain in compliance to avoid the risk of major setbacks. Additionally, making the required functionality and performance improvements helps you advance through the product development process more efficiently.
Clovis’s Life Sciences Consulting provides validation services to many of the nations premier pharmaceutical, biotechnology and medical device companies. By combining strategic consulting with project based services, we deliver the talent and resources you need to address the validation challenges your organization is currently facing.
Practice Areas
- Equipment Validation
- Process Validation
- Test Method Validation
- New Facility Validation
Whether you need a short-term resolution or a strategic solution we will provide the expertise and resources you need to advance your product to the market safely and effectively.
Areas of Expertise
- Sterilization Validation
- Packaging Validation
- Servicing Validation
- Equipment Validation
- Process Validation
- Software Validation