CTD is now more easy with eCTD
      What we Do:
    • We Write Dossier/DMF
    • We Convert it in eCTD Format
    • We Submitt the same to Authority

    Be carefull Many money grabers are now threatning Industry that eCTD is something very different and you are going to be in trouble and starts grabing money from your pocket,don't be in their words they are just misguiding you,its a esiest and very simple procedure wich is less complicated than paper submission.

    eCTD is not a rocket science it's regular Digital technology in PDF form which you have to submitt instead of Paper Copy.

    Go through this detailed guideline of eCTD and if you do not understand ask for guidence till if there is any confusion just ask us to do this work by CPPL expert team for you and they will do it in regulor cost and not with additional cost.eCTD Guideline

    In your all kind of regulatory compilations,creation of documents and submission Cyclone Pharmaceuticals Pvt Ltd,the Pharmaceutical Consultants of India will help at every stage.Unlike other consultants we have team with QA,QC ,Production and Regulatory sector so review of documents ,compilation of dossiers and Query answering is ultimately easiest task for CPPL

    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

      Why to Choose CPPL as your Regulatory and Dossier Partner
    • Knowledge of Pharmaceutical Technologies
    • Knowledge about formulation and analytical techniques
    • Minimises time of registration with it's Perfect dossier service
    • Complete Support for Generating documents like PV,AMV,Stability
    • Comparativelly very Low Cost (Do not compaire with computor operators who provide Dossiers free of cost)
    • Honest servives ,we says yes if it is possible and no if having any difficulties
AIM
  • To serve Pharmaceutical Industry with best quality services and to bring a Quality culture in Documentation and regulatory services
  • Note : CPPL The best regulatory service providers of India do not compete with any other service providers because we know we are best