Perfect Pharmaceutical Consultants
writes Dossiers / DMFs for Pharmaceutical Formulators, Bulk Drug Manufacturers, Intermediates sellers, Traders, Pharma packaging manufacturers which will enable them to register and export their Products to various countries around the world.

Why choose us?

Over 20 years of Experience Extensive experience with API, Pharmaceutical Dosage Forms ,Excipients , Packaging materials development issues, including Preclinical Pharmacology, Toxicology, Clinical Trials , Manufacturing, QC & QA , Product Development ,Stability studies, HPLC/GC Analysis, Chiral Chemistry, Polymorphism, X Ra Diffraction,


PPC is a professionally managed company with roots back to 1987.
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We can provide the following Patent related services ;

  • Core Regulatory Services

    CTD and eCTD submissions on all
    types of drug products...
  • Other Regulatory Services

    Follow-up with MOH till the registration documents are accepted and approval letter is issued...
  • DCGI - Indian FDA

    PPC can assist Pharmaceuticals / Food / Cosmetic / Medical device companies...
  • CTD - Dossiers

    Dossier is an integral Part of any registration application for Marketing Authorization...
  • Drug Master File - DMF

    Drug Master File is a technical documents containing CMC part...
  • Packaging Material DMF & Excipients

    Primary Packaging material is the material which is directly...
  • Regulatory Submission

    PPC specializes in compilation of
    Drug master file for pharmaceutical products...
  • Regulatory Medical

    Medical writing for pharmaceutical industry involves regulatory documentation ...

    PPC Dossier/ DMF writing service will help you by

  • Savings of Manpower training & Recruitment
  • Reduction of Marketing Authorization Rejection
  • Simplify and systemize your regulatory submissions
  • Save money by avoiding costly mistakes through self submissions
  • Quicker FDA Submission
  • Increase of Exports and reach in various countries

    What our clients saying