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.

Longueuil, Quebec SYLLA CONSEILS INC. 2018-01-30
Laval, Quebec Hay Pharma Consulting 2018-05-01
Montreal, Quebec Access Pharma Group 2018-01-30
Montreal, Quebec Canadex Laboratories inc 2018-01-30
Montreal, Quebec Product Life Group 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

Release of Proposed IMDRF Document: Definitions for Personalized Medical Devices

Release of Proposed IMDRF Document: Definitions for Personalized Medical Devices

The International Medical Device Regulators Forum (IMDRF) recently published a Proposed Guidance Document titled Definitions for Personalized Medical Devices (the “Guidance”). The Document is open for public consultation and has been posted on the IMDRF website for comments from the public.

Health Canada Continues to Tweak Requirements for MDSAP Transition

Health Canada Continues to Tweak Requirements for MDSAP Transition

Manufacturers who sell medical devices in the Canadian market are required to submit MDSAP certificates by December 31, 2018. The Medical Device Single Audit Program (MDSAP) is an international harmonization initiative that allows a single audit to meet the regulatory requirements of five jurisdictions (Canada, United States, Brazil, Australia and Japan).

Health Canada Notice on ICH Selection and Justification of Starting Materials for the Manufacture of Drug Substances

Health Canada Notice on ICH Selection and Justification of Starting Materials for the Manufacture of Drug Substances

On April 4th, 2018 Heath Canada issued a Notice to announce its implementation of the ICH Q11 final guidance document on Questions and Answers: Selection and Justification of Starting Materials for the Manufacture of Drug Substances. This version of ICH Q11 Question and Answers was initially published in August 23, 2017 by the ICH Expert Working Group.