Working directly with experts and regulatory authorities around the world, our experienced in-house regulatory affairs team finds the most advantageous routes for our products in the various markets in which we operate.
By familiarising ourselves with national requirements, we ensure that we gain timely approvals for our products and that we comply with the directives and guidelines for the quality, safety and efficacy of our products prior to placement in the key global markets.
Our regulatory affairs team works in close collaboration with our global external business partners to secure regulatory approvals by the relevant authority prior to placement of our products for these markets.
The evolving and dynamic regulatory environment has resulted in legislation changes across many of the countries in which InQpharm has a commercial interest. Based on the research data generated, the team provides advice and guidance to internal and external partners to ensure successful and timely regulatory approvals with maximum product label claims.