CSV: MORE than writing test scripts
Join us Wednesday, May 20th at 2:00pm EST
When you think of validating a computer system, what comes to mind? For many, it’s testing to verify the system performs as needed, and maybe a test plan, but not much else. There’s a lot more to consider when validating a computer system than configuration, functional, and requirements testing (aka IQ, OQ, and PQ, respectively). Has a risk assessment been performed? Does your testing team have the time and/or experience (regulatory, domain, system) to create and execute test scripts? Has the appropriate documentation (validation plan, configuration/design specification, etc.) been developed and reviewed? Are your SOPs complete and up to date? Thinking you can get by with using a generic validation plan or just the vendor’s provided scripts could put your company at risk during an FDA audit. Did you know that a great number of 483s are currently issued for lack of or poorly documented validation of the intended use of the system and undocumented validation processes?
In this one hour webinar, we will review critical success factors to streamline your validation process, saving you time and money. We will also go over recommended validation documentation that satisfies any FDA audit. Lastly, we will explore what it takes to ensure validation success. So join us for an hour and learn why successful Computer System Validations are more than just writing and executing test scripts.
Who Should Attend:
Register Here: http://goo.gl/6GrnNy
You will have the opportunity to speak directly with a Computer System Validation expert and receive real-time answers. Take home ideas and checklists to ensure that your CSV project is a success.
This is a complimentary hour long presentation including a Q & A section.
131 Continental Drive, Suite 303
Newark, DE 19713
302-731-5290 | www.csolsinc.com