Life Sciences Leadership Team

Wendy has worked with leading pharmaceutical companies and global regulatory bodies in coordinating the compilation, production and distribution of compliant FDA and EMA submissions utilizing electronic document technologies. She has also developed, trained, supported and maintained global systems and processes in order to submit compliant drug submissions electronically to health authorities. Wendy holds a bachelor’s degree in international mass communications with a dual minor in international business administration and Chinese Studies from Pennsylvania State University.

John Lorenc directs electronic submission and regulatory requirement initiatives that impact the medical device industry. He has advanced experience with machine-to-machine submission requirements to global UDI databases, including US FDA GUDID, EU EUDAMED, and China NMPA UDID. John represents Reed Tech in membership with MedTech Europe, and actively participates in electronic submission pilots to regulator UDI databases.

Gary Saner is a subject matter expert on medical device Unique Device Identification and other structured content reporting to regulatory agencies and commercial organizations. He has over 30 years of experience in software development, process management and data administration with the last 15 years focused on the life sciences industry. He serves as Co-Chair of the industry’s Structured Product Labeling Technical Team and on the Advisory Board of the Medical Devices Group.

Andrew Ethridge currently leads the product group focused on the needs of pharmaceutical companies in the areas of regulatory compliance and product data management for US FDA and emerging requirements from Health Canada and other health authorities. He received his MBA from Keller Graduate School of Management at DeVry University, a BS in Criminal Justice from Chestnut Hill College.