Cyclone Pharma has experts for eCTD Compilation and conversion servcies,CPPL had developed first eCTD software when eCTD Draft guidelines have been declared for Industry.Cyclone team have deep knowledge and understanding of eCTD Compilation and conversion.
What we offer is a comprehensive range of services to assist in regulatory compliance. Our team at Cyclone Pharmaceuticals Pvt Ltd, a leading pharmaceutical consultancy in India, specializes in writing dossiers and converting them into eCTD format. We also handle the submission process to the appropriate regulatory authorities. Our eCTD conversion software, developed by our expert consultants at CPPL, simplifies the process and significantly reduces submission costs compared to market standards.
For all your regulatory compilations, document creation, and submission needs, our team at CPPL is here to assist you at every stage. Unlike other consultants, we have a dedicated team with expertise in QA, QC, Production, and Regulatory sectors, ensuring thorough document review, dossier compilation, and prompt query responses.
Our regulatory consultancy services at Cyclone Pharmaceuticals have a proven track record of delivering high-quality solutions at the lowest cost. Many times, our compiled documents have been accepted by regulatory authorities without any queries. We are always updated with the latest regulations and can provide accurate compilation in various formats, including Drug Dossier, DMF, CTD, ACTD, KDMF, USDMF, eCTD, EUDMF, USDMF, and more.
Regulatory consultancy services of Cyclone Pharmaceuticals are proven services with highest Quality and Lowest cost.
Our compiled documents many times are being accepted by regulatory authorities without single query. CPPL team is always
alert for new updations in regulations provides perfect Drug Dossier, DMF, CTD, ACTD, KDMF, USDMF. eCTD, EUDMF, USDMF and
other format compilation.