Regulatory Compliance

CapsCanada’s range of capsules are fully compliant with global regulations for pharmaceuticals and dietary supplements, but we also provide dedicated support to guide you through the complexities of the regulatory process and fast-track your products to approval.

With CapsCanada as your development and manufacturing partner, you benefit from personalized, streamlined support across the full scope of your project, which is especially valuable when it comes to regulatory affairs. By working continuously with the team that has helped to create your product, starting with the reference material, you can be confident of the accuracy of the required regulatory documentation, and that it is properly filed with the relevant agencies on time.

Whether you are submitting a New Drug Application (NDA), Abbreviated New Drug Application (ANDA) or international equivalent, CapsCanada provides seamless access to all the documentation you need, including Certificates of Analysis (COAs) and Certificates of Composition, and will help prepare your documents for regulatory submission. Our compliance experts will advise you every step of the way as you navigate the process.