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.

Toronto, Ontario dicentra 2018-01-30
Brampton, Ontario Abaci Regulatory & Quality Consulting Inc. 2018-01-30
Laval, Quebec Consultpharm Inc. 2018-02-01
Montreal, Quebec Proficio Scientific Affairs 2018-02-21
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

Validation Rules for Regulatory Transactions Submitted in the electronic Common Technical Document (eCTD) Format

Validation Rules for Regulatory Transactions Submitted in the electronic Common Technical Document (eCTD) Format

Late last year, Health Canada announced the revised validation rules for regulatory transactions in the electronic Common Technical Document (“eCTD”) format.

Health Canada’s Guidance on Applications for Medical Device Investigational Testing Authorizations

Health Canada’s Guidance on Applications for Medical Device Investigational Testing Authorizations

In late 2017, Health Canada released a draft guidance document to assist sponsors, manufacturers, and importers on the authorization process for investigational testing of medical devices. The draft guidance, titled “Applications for Medical Device Investigational Testing Authorizations”, is open for consultation and supersedes the previous guidance document from 1999 (“Preparation of an Application for Investigational Testing – Medical Devices”).

Guidance Document - Guidance for Manufacturers of Human Immunodeficiency Virus (HIV) Rapid Diagnostic Tests (RDTs) for use at the Point of Care or for Self-Testing

Guidance Document - Guidance for Manufacturers of Human Immunodeficiency Virus (HIV) Rapid Diagnostic Tests (RDTs) for use at the Point of Care or for Self-Testing

In late 2017, Health Canada published a new guidance document concerning HIV RDTs, titled “Guidance for Manufacturers of Human Immunodeficiency Virus (HIV) Rapid Diagnostic Tests (RDTs) for use at the Point of Care or for Self-Testing” (the “Guidance Documents”). The Guidance Document provides manufacturers of Class IV HIV RDTs for point of care or self-testing applications with specific guidance on the analytical and clinical data as well as labelling considerations as part of the device application process.