05/31/2017 - Minimizing Risk in Medical Device Material Selection Are you selecting materials for use in a medical device and overwhelmed by the dizzying array of material options? Dr. Brian Ralston shares the process CPG uses to help clients select and test materials to minimize risk and maximize safety, efficacy, and prospects for regulatory approval.  

02/23/2017 - Cleanliness in Medical Devices Learn what happens when cleaning processes are not properly verified and validated, how to establish the number of samples to test, how to test for device cleanliness, and how to establish acceptable residue limits. 

12/08/2016 - Degradable Products in Medical Devices This webinar focuses on techniques to identify and quantify degradation products in in vitro and in vivo environments. Knowledge of the kinetics of degradation products and the degradation pathway will allow researchers to validate simulated in vivo environments and to establish risk profiles for degradable products based on biocompatibility concerns. The techniques are applicable to materials for permanent implants and to biodegradable materials.