(CPVP) Certified Process Validation Professional™

Ensure Excellence With Our Certified Process Validation Professional Program

Companies in the pharmaceutical, biotech, medical and cosmetics industries are required to abide by FDA compliance standards. At CfPIE, our FDA process validation training ensures your team maintains a level of excellence in process validation, keeping your facility compliant. CfPIE is dedicated to providing high-quality pharmaceutical validation certification training, enabling your team to master the process of end-to-end process validation. 

Key Skills You Can Gain Through Our CPVP Program

If you are tasked with process validation in the pharmaceutical, biotech and cosmetics industry, you already know that FDA compliance is a crucial part of the process. When you invest in the CfPIE process validation professional certification, you are making sure your teams are trained, educated and consistently up to date with compliance standards. Here are a few of the key skills you can gain through FDA process validation training with CfPIE:

• Equipment and system qualification
• Complete validation documentation
• Continuous process verification (CPV)
• Validation protocol execution

When you commit to the CfPIE Certified Process Validation Professional (CPVP) program, you are giving your teams the top education in process validation for the pharmaceutical, biotech and cosmetics industry. Our teams are thorough, consistent and reliable with their training, ensuring a complete, customized process for your teams and their specific workflows.

Why Our CPVP Certification Works

The CfPIE certified process validation professional program is designed with excellence in mind, providing high-quality FDA process validation training for your team. By offering a thorough and detailed approach to process validation, the CPVP certification covers all aspects of the work, guiding you through every stage in extreme detail. Upon completing the course, you can experience benefits such as:

• Improved product quality and manufacturing.
• Up-to-date approach with FDA compliance.
• A method-driven application approach.
• Strengthened understanding of practices.

For pharmaceutical teams and manufacturers, staying compliant is beyond important, it is critical. Without compliance, entire batches of product can be rendered unusable and people can be put in danger. Not only does the CPVP program ensure compliance, it elevates product quality to an excellent level.