Canada Operations

MetaPharm Inc. has gathered many years of experience in clinical research with local CROs in Canada, before the company, in response to increasing requests by its clients, decided to establish its own Canada business. It is managed by a highly educated and committed local team with expertise in drugs, biologics, and devices (Class I-III).

For you as a Global client, MetaPharm Inc. project management and operations teams based in Canada bring clear advantages: with your main contact person based in Canada, communication and collaboration are streamlined to meet different requirements and expectations. Standard operating procedures and working procedures are harmonized; the high MetaPharm Inc. standard of quality data is ensured at all times.

MetaPharm Inc.’s experts will accompany you through all stages of your product’s journey. Your clinical trial will benefit from our experience in developing regulatory strategies for Health Canada and the FDA, in addition to our expertise with NIH and DoD federal grants.

Our experienced Canada team will give you regulatory support during pre-IND, IDE, de novo, and other formal meetings, as well as scientific advice. Our experts will accompany your complete submission process in Canada and the US.

“We strive to build collaborative long-term relationships with our partners to optimize the path to market approval.”