This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

September 21-24, 2020
Proudly part of BioPharm AmericaDelivered Digitally | US Eastern Daylight Time

Liliana Omar
Regulatory and Quality Project Director at Covance


Liliana Omar is a Regulatory and Quality Project Director at Covance Medical Device and Diagnostic Solutions with experience in medical device and pharmaceutical industries focusing in areas of product development, manufacturing, quality systems, regulatory affairs and regulatory compliance.

Liliana supports client regulatory and quality system needs, provides advice to the client, and works with the regulatory authorities and Notified Body representatives to obtain product clearance or approval. Liliana has experience with medical devices, drugs, drug-device combination products and metal components for medical devices. She has worked for organizations with different operational models including virtual companies, manufacturers and contract manufacturers.

Agenda Sessions

  • EU/MDR/IVDR Combination Product and Companion Product Considerations