Understanding the complexities surrounding the regulatory requirements and how to implement them plays a critical role throughout the development and ongoing maintenance of any new drug.
By getting it right, first time, and having an experienced team to hand to give you high level strategic advice and support to keep you on track, greatly increases your product’s chances of getting to market and reaching patients.
The ANKofis team has hands-on and in-depth experience across all therapeutic areas and all stages of a drugs development. We understand how to incorporate the regulatory requirements into your development plan, taking an impartial and independent view, helping you to focus on the right activities and end-points to assist you in gaining regulatory approval in Turkey.
We understand how the Turkey differs from other regulatory requirements in EU, N.America, Asia and Oceania, and can give you practical support to gain approval for your product.
Our aim is to help you to save time, costs and resources and increase your chances of success.
