Pharmaceutical and Healthcare

The focused team of scientific consultants in Cantox's Pharmaceutical and Healthcare (P&H) Group can help develop strategies and provide expert advice on all aspects of product development programs in various areas with offices in the United States, Canada, Europe & Asia.

Whether it is a pharmaceutical product, biotech, natural health, combination, cosmetic & personal care products, or medical devices, our toxicologists and regulatory scientists can help address your needs. The Cantox P&H Group can assist in the following areas:

• Strategic Planning
  cost effective development, integrate nonclinical program with clinical development, anticipate and overcome regulatory hurdles.
   
• Program Management
  design and assist with pharmacology and toxicology programs from protocol development, CRO (Clinical Research Organization) selection and placement/monitoring of studies, study audits, preparation of integrated summaries, review of final reports.
   
• Regulatory Affairs
  regulatory strategies, preparation of CMC (Chemistry Manufacturing and Controls) (including biologic/biotech products), nonclinical and clinical summaries and tables, from pre-meeting packages to filing full submissions to conduct clinical trials or market registration world-wide.
   
• Consulting and Expert Advice
  assistance in lead candidate selection, due diligence activities, third party assessments, interpretation and positioning of date, liaison with regulatory agencies worldwide and responding to questions.

With diverse and in-depth experience in pharmaceutical development, our resourceful and innovative team consists of board-certified toxicologists, regulatory affairs specialists and scientific writers.

We succeed when our clients succeed and we have proven this time and time again!

Contact our Pharmaceutical & Health care Consultants: info@cantox.com