Performance Validation has the proven knowledge and experience to support the delivery of your cutting edge medical devices, drug and combination products to market. Whether it’s assistance ith the development/qualification of process parameters for a Bi-Layer tablet press, to providing technical assistance for the design of a pen injection assembly process, PC is your one stop validation provider.
Performance validation provides peace of mind by supporting your project needs from start to finish; from assisting with the delivery of user requirements that ensure the success of your project, to providing the validation documentation needed to address regulatory agency requirements (FDA. EMA, etc…) When working with with combination products, our knowledge and expertise with 21 CFR Part 210/211 and 820 allows us to provide the guidance needed to ensure that you are meeting both device and drug regulatory requirements.
If you are attending the 2016 ISPE annual meeting September 18-20, in Atlanta GA please stop by Booth 818 to meet members of the Performance Validation team to learn about our expertise and how we might be able to help you on your current or future project.
We hope to see you there!