Preformulation, or the physicochemical characterization of your Active Pharmaceutical Ingredient (API) in light of the intended route of administration and dosage form, is an important phase pharmaceutical development.
We have the combination of development expertise, manufacturing equipment and state-of-the-art facilities to be your strategic partner for reliable, cost effective long term supplies of your intermediates and API.
Apnar's Validation Solutions group strives daily to provide superior service and support in a consistent, cost-effective manner
As an integral part of product development, Apnar Pharma provides an analytical method development service. Additionally, Apnar Pharma also provides a standalone method development service, a method validation service, routine testing, and stability testing services in compliance with FDA/EMA and ICH guidelines. Apnar Pharma has experience in providing analytical services for regulatory submissions. We provide timely support for regulatory submissions and responding to regulatory deficiencies.