DMF Cyclone Pharma is highly regarded as the preferred Regulatory Consultant in India, with a proven record of successfully writing over 3000 dossiers. The trust of our clients is of utmost importance to us, and we have earned that trust over a considerable period of time.
Cyclone Pharmaceuticals Private Limited, the Dossier consultant of India, boasts extensive experience in writing over 3000 distinct dossiers for various clients and countries. Our expertise in dossier writing has led to the development of numerous products, and we possess ready dossiers and technologies for manufacturing, with complete validation support at your manufacturing unit. Through our meticulous compilation and review process, we aim to minimize queries on documents, ensuring that our dossiers are readily accepted by regulatory authorities
Our experts, well-versed in ground-level challenges associated with dossier and drug master files, frequently field inquiries from authorities. Cyclone Pharmaceuticals Pvt Ltd, as the Pharmaceutical Consultants of India, offers comprehensive assistance throughout all stages of regulatory compliance, document creation, and submission. Unlike other consultants, our team comprises professionals from the QA, QC, Production, and Regulatory sectors, making document review, dossier compilation, and query answering effortless for CPPL.
Our regulatory consultancy services have been proven to deliver the highest quality at the lowest cost. Many of our compiled documents have been accepted by regulatory authorities without a single query. At CPPL, we stay up-to-date with regulatory updates and provide flawless compilation of Drug Dossiers, DMF, CTD, ACTD, KDMF, USDMF, eCTD, EUDMF, USDMF, and other formats.