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Welcome to the Ontario community site, part of RAPS’ global online community, Regulatory Exchange or “RegEx.” By being a member of RAPS, not only are you connected to 30,000+ regulatory professionals worldwide, but you also have access to a vibrant regulatory community right here in your geographic region. If you are a RAPS member, log in for full access to the member directory and the discussion board.

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REGULATORY JOB OPENINGS

Regulatory Affairs Specialist | University of Pennsylvania Healthcare System

6 days ago

Philadelphia, Pennsylvania, Regulatory Affairs Specialist-The UPENN Coordinating Center for the RadComp trial, a national multi-site randomized clinical trial (www. Radcomp.org) seeks an experienced...
Director of Quality Management | Kindred Hospitals

7 hours ago

Philadelphia, Pennsylvania, What makes Kindred Healthcare a great place to work? Our people, of course! Our clinicians answer this special calling because they have a fundamental, internal drive...
Quality Clinical Outcomes Manager | Inspira Health

one month ago

Mullica Hill, New Jersey, Quality Clinical Outcomes Manager Inspira Health Mullica Hill, New Jersey One of the region’s leading networks of healthcare providers, Inspira Health is seeking a...
Quality Coordinator, Peer Review | Inspira Health

one month ago

Mullica Hill, New Jersey, Quality Coordinator, Peer Review Inspira Health Mullica Hill, New Jersey One of the region’s leading networks of healthcare providers, Inspira Health is seeking a...
Kavo Senior Regulatory Affairs Specialist (Hatfield, PA) | Envista

10 months ago

Hatfield, Pennsylvania, KaVo Kerr is a cohesive organization comprised of two global leaders, united to provide dental excellence and serve as a single premier partner for the dental community. KaVo...

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Upcoming Events List

Biologics CMC: Regulatory Challenges and Trends

1/20/2022 9:00:00 AM

Receive an overview of chemistry, manufacturing and control (CMC) regulatory requirements and best practices associated with biologic and biosimilar products...
Software as a Medical Device

1/25/2022 9:00:00 AM

Member: $970 |Nonmember: $1,150 Join regulatory experts to explore evolving global regulatory requirements affecting SaMD, including determining when...
Dangerous Documents: Avoiding Land Mines in Your Records and Emails

1/27/2022 8:00:00 AM

Members: $175 | Nonmembers: $200 Learn to analyze and revise written documents to protect yourself and your organization from unwelcome surprises....