Transcat offers a wide variety of validation services that meet FDA, ICH, and many European standards. Although our primary focus is on that of the pharmaceutical and biologics industries, we also perform many required studies for food and beverage, cosmetic, industrial, and medical device companies as well.
Since our customers are regulated by either GMP, ASTM, GLP, or the Code of Federal Regulations, we understand that one off the shelf protocol template would not be enough to satisfy each of our customer's diverse needs. For this reason, we customize our protocol packages to meet the specific quality system of every customer that we service. The quality department is allowed to review our documents before we arrive on site to ensure that there are no gaps and all regulations are met.
In addition to customization of protocols, Transcat also understands the need for flexible scheduling and service options, in order to minimize cost and disruptions. We often work around production schedules, on a second shift, in order to maximize our customer's operational times, which diminishes interruptions of the day to day business. Our services can be protocol generation only, execution of customer protocols, or the full suite of protocol generation and execution.
No matter what service is requested, a technical validation representative will assist our customers in determining the best scope of work for each job and provide a detailed quote that clearly establishes the scope of the job. There is no opportunity too large or too small for our team. We look forward to partnering with you on your next Validation service.
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