CAPRA BENEFITS

The Canadian Association of Professionals in Regulatory Affairs (CAPRA) is an organization dedicated to providing its members with opportunities to enhance their professional development and maximize career opportunities. Whether you are a student, an entry-level associate or an experienced executive, a membership with CAPRA is a must.

We foster learning, networking and professional excellence of our members. We will build and strengthen relationships with governmental agencies, scientific experts and industry educators in order to create an affordable, professionally fulfilling and academically enriching environment for our members.

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WHY JOIN CAPRA AS A STUDENT?

Introduction to Regulatory Affairs and the Regulatory Affairs Profession

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CONSULTANTS

A listing on the CAPRA website is available to consulting companies whose primary focus is Regulatory Affairs, Clinical Research, Quality Control or Compliance (GCP, GLP, GMP) for pharmaceuticals, biologics, veterinary drugs, medical devices, cosmetics, over-the-counter products, or natural health products.

Dundas, Ontario Mapi 2018-01-30
Airdrie, Alberta TJS Technical Services Inc. 2018-11-13
Laval, Quebec Grieb Consulting / VG Solutions Inc. 2018-01-30
Longueuil, Quebec SYLLA CONSEILS INC. 2018-01-30
Barrie, Ontario SMI Solutions 2018-01-30

ADVERTISE WITH CAPRA

Reach CAPRA members through the NOC (News of Course), or place an employment ad in our listings.

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EMPLOYMENT LISTINGS

Available to CAPRA Members

Planning to place an employment advertisement through CAPRA/ACRP? Looking for a new career opportunity? If so, you have come to the right place! CAPRA now has over 900 members in the regulatory affairs field!

Job Seekers: Scroll through our most recent postings, your dream job maybe at your fingers tips!

Employers: Regulatory professionals are difficult to find. Win the competition for talent, by advertising in CAPRA. Our email employment notice service brings you access to hundreds of top class, experienced professionals. One of them may be just whom you are looking for!

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CAPRA BLOG

Device Advice: Health Canada Launching a New Pilot Project to Formalize Regulatory Advice Framework for Medical Device Manufacturers

Device Advice: Health Canada Launching a New Pilot Project to Formalize Regulatory Advice Framework for Medical Device Manufacturers

Health Canada recently announced it is the process of formalizing a meeting framework called "Device Advice: Pre-Clinical Meetings", where medical device manufacturers will be able to receive advice and recommendations for investigational testing protocols.

Health Canada Update on Investigational Testing Authorizations for Medical Devices

Health Canada Update on Investigational Testing Authorizations for Medical Devices

Investigational Testing Authorization (ITA) issued by Health Canada, allows for the testing of Class II, III, and IV medical devices with human subjects. For unlicensed devices, the submission of an ITA is required to establish new safety and effectiveness data, however, ITAs are also required for licenced medical devices when establishing safety and effectiveness for new indications.

Toward Global Harmonization - Health Canada to Adopt IMDRF Table of Contents Format for Class III and IV Applications

Toward Global Harmonization - Health Canada to Adopt IMDRF Table of Contents Format for Class III and IV Applications

In another move toward global harmonization, by April 1, 2019, medical device manufacturers will be required to submit premarket applications for Class III and Class IV applications in Canada in either the International Medical Device Regulators Forum (IMDRF) table of contents (ToC) format or Health Canada format.