Since 2001, Tanis Technical has been helping a wide range of international Life Sciences companies and equipment manufacturers document, test and validate their systems to ensure GMP compliance. In addition to equipment qualification services (facility, utilities, packaging, process and lab equipment) we specialize in IT validation services, including hardware, servers, software and networks--we are your one-stop shop for Validation services!
Our customers include regulated companies and those who supply them:
- Pharmaceutical
- Nutraceutical
- Medical Device
- Alcoholic Beverage
- Packaging and Process Equipment Manufacturers
President Ken Woychesko has combined his more than 16 years of experience in the pharmaceutical, information technology, and software testing fields to lead Tanis Technical's team of cGMP compliance professionals.
In today's complex regulatory environment, GMP requirements are often changing and Quality Assurance and Validation resources are stretched. Maintaining compliance is a difficult task for many manufacturing facilities. Increasingly, pharmaceutical, biopharm and nutraceutical companies are outsourcing their qualification and validation services activities. An outside validation supplier encounters new equipment on a regular basis, and will be able to augment your resources should you have an experience or availability gap. This results in shorter and more efficient validation cycles, allowing you to increase compliance and decrease production delays.
Let us help augment your pharma QA and Validation program to increase compliance, sales, internal controls, and efficiency by using our Validation Services Team to develop Qualification Protocols, SOP's, specification documents, best practices and guidelines.
Contact us to find out how Tanis Technical can streamline your validation process.
