Cyclone Pharma has support for carrying out analytical development and validation from numerous authorised and approved laboratories in India.We assume responsibility for assisting clients with regulatory matters, keeping a careful eye on your project, and completing the necessary tasks.We are renowned for our accuracy and fineness.
The Analytical Method Validation (AMV) is a crucial part of any Dossier or DMF, yet many manufacturers tend to neglect it, resulting in delays in the registration of pharmaceutical products. CPPL recommends that manufacturers concentrate on the AMV while compiling DMF, CTD, ACTD, KDMF, USDMF, eCTD, EUDMF, USDMF, and other format of dossiers. We provide services to perform analytical development and AMV and suggest appropriate ways to do s.
There is often confusion among technocrats about the necessity of AMV in a dossier, leading to myths. However, our technocrats at CPPL can advise you about the technical input of AMV and save your efforts and money. It is crucial to ensure technical perfection in AMV, as some consultants may offer low-cost AMVs without any knowledge of Analytical Method Validation. Therefore, it is important to be cautious when dealing with such consultants and raise questions if necessary.