About Us
Our Mission
“Provide a wide range of specialized services covering all regulatory needs from discovery to commercialization of a drug or medical device.”
Our Mission
“Provide a wide range of specialized services covering all regulatory needs from discovery to commercialization of a drug or medical device.”
Our Expertise | Our Values
Validapro has international compliance expertise including FDA, EMA, ANSM, ANVISA, Japan and Health Canada, which closely combines Quality and industrial approach. The approach developed for each project is focused on meeting regulatory expectations and on the effectiveness of solutions proposed and developed with respect and transparency in partnership with our customers.
Engineering
Our approach, applied from R & D to industrial manufacturing, covers the design of premises, the choice of equipment and utilities for manufacturing and packaging (primary and secondary) of oral products, sterile and non-sterile, dry forms, semi -liquids and liquids in the pharmaceutical, cosmetics, natural health products, medical devices and biotechnology areas.
Compliance
Validapro’s regulatory expertise underpins all the projects carried out and allows the application of the “Lean” and “GMP” concepts to ensure compliance with regulatory expectations while optimizing operational performance.
Our History
Validapro is present on both side of the Atlantic with an European base in Toulouse, France and an American base in Montreal, Canada.
Founded in 1993 by Compliance Services Managers of major pharmaceutical companies, Validapro began by offering its services in validation and qualification and then broaden its expertise to the overall compliance projects.
Present in France since 1998, we can offer our expertise on the specific regulatory requirements of the FDA.
The Validapro’s team is made up of professionals offering a wide range of expertise, enabling them to get involved in the heart of your processes by offering lean management in project management approach combining the profitability of your production processes and your regulatory requirements.
Our Expertise | Our Values
Validapro has international compliance expertise including FDA, EMA, ANSM, ANVISA, Japan and Health Canada, which closely combines Quality and industrial approach. The approach developed for each project is focused on meeting regulatory expectations and on the effectiveness of solutions proposed and developed with respect and transparency in partnership with our customers.
Engineering
Our approach, applied from R & D to industrial manufacturing, covers the design of premises, the choice of equipment and utilities for manufacturing and packaging (primary and secondary) of oral products, sterile and non-sterile, dry forms, semi -liquids and liquids in the pharmaceutical, cosmetics, natural health products, medical devices and biotechnology areas.
Compliance
Validapro’s regulatory expertise underpins all the projects carried out and allows the application of the “Lean” and “GMP” concepts to ensure compliance with regulatory expectations while optimizing operational performance.
Our History
Validapro is present on both side of the Atlantic with an European base in Toulouse, France and an American base in Montreal, Canada.
Founded in 1993 by Compliance Services Managers of major pharmaceutical companies, Validapro began by offering its services in validation and qualification and then broaden its expertise to the overall compliance projects.
Present in France since 1998, we can offer our expertise on the specific regulatory requirements of the FDA.
The Validapro’s team is made up of professionals offering a wide range of expertise, enabling them to get involved in the heart of your processes by offering lean management in project management approach combining the profitability of your production processes and your regulatory requirements.
Our Leaders
Luc Dubois
Luc has more than 30 years of experience in the pharmaceutical and biotechnology industry. He founded Validapro in 1993 in Quebec and opened a satellite office in Europe in the spring of 1998 in Toulouse, France.
Before founding Validapro, Luc worked for companies such as Glaxo Wellcome and Bristol Myers Squibb.
He is recognized as a leading expert in international inspection preparation and has accompanied our clients on over 70 FDA inspections, all of which have been successfully completed.
Our Clients
