The goal of validation is to acquire data that demonstrates how your system, process and/or equipment will perform to expectations while ensuring product purity, safety, and efficacy on a consistent basis. In preparation for validation, we can write a protocol ‚ a detailed plan of how the validation will take place and what equipment will be used. Prior to validation, an FDA Qualification of your equipment and/or systems may also be performed. A validation service package from Transcat could include installation, operational and performance qualifications on the equipment used in pharmaceutical practices.
Documentation of FDA Compliance
Our teams of experts stand ready to support your organization in achieving critical FDA compliance and your specific quality system. By partnering with a reliable validation services provider, companies can obtain scientific evidence demonstrating that the equipment utilized in their facility operates as prescribed and therefore generates quality products consistently. Validation proves that there is control over your equipment that could potentially jeopardize quality.
Transcat's proven record of expertise will help you comply with a full range of cGMP and regulatory requirements. Request a quote to experience flexibility in scheduling, as well as service options that consider your budget and scheduling demands.
