McCarthy Consultant Services Inc. (MCSI) provides expert regulatory affairs consulting. As a global industry leader, MCSI understands the importance of sound regulatory management and client satisfaction.

Regulatory affairs services for the pharmaceutical and medical industries

Our ability to tackle difficult and complex regulatory issues quickly and efficiently has made MCSI a trusted and valued provider of regulatory affairs services to the biotechnology, pharmaceutical, medical device, natural health product, food and cosmetic industries.

MCSI is considered a major asset by Canadian, foreign and virtual organisations conducting business in Canada, the US and EU. With our regulatory capabilities, we can successfully guide your products through complicated regulations.

MCSI has built worldwide, strategic alliances with organisations, allowing us to offer our clients access to the UK, Australia, Japan, the Nordic countries, Russia and Eastern Europe.

Expert opinions and outsourcing of regulatory affairs

We can provide a range of services, from offering well-established, multinational companies an expert opinion, to outsourcing all regulatory affairs for small startup firms.

Whether it is regulatory strategic planning or a full product submission, MCSI has an expert team of regulatory associates who can get your project completed.

Regulatory affairs and quality assurance services

Along with regulatory strategic planning and preparation and filing of product applications for drugs, medical devices, natural health products, MCSI also offers a wide range of other regulatory affairs and assurance services, including:

  • Preparation of applications for drug establishment licences, medical device establishment licences and site licences
  • Preparation of drug master files
  • GMP design, audits and training
  • SOP writing and training
  • Design and management of quality assurance / quality control systems
  • Validation
  • Due diligence
  • Government liaison

Regulatory and quality assurance projects

MCSI has worked on various regulatory and quality assurance projects, including:

  • New Drug Submissions and New Drug Applications
  • Abbreviated New Drug Submissions and Abbreviated New Drug Applications
  • Supplemental New Drug Submissions and Supplemental New Drug Applications
  • Investigational Testing Application and Investigational New Drug Application
  • Drug Identification Number Applications (DIN)
  • Natural Product Number Applications (NPN)
  • Medical Device License Applications
  • Good manufacturing practices (GMP) system design and management
  • Standard operating procedures (SOP) writing
  • Drug Master Files
  • Rx-to-OTC switches
  • Labeling and advertising review

To discuss your regulatory outsourcing needs, please get in touch with us using the enquiry form below.