Registration dossier” of the pharmaceutical product is a document that contains all the technical data (administrative, quality, nonclinical and clinical) of a pharmaceutical product to be approved registered marketed in a country....
Technical Dossier Services provide comprehensive documentation for regulatory approval of chemical substances, pharmaceuticals, and agrochemicals. These services include data compilation, safety assessments, toxicological studies, and efficacy...
Services offered by PHARMA HOUSE Dossiers (CTD, e-CTD, ANDA and ANVISA) (All Country Specific, As per client request) DMFs(CTD, e-CTD)(Open &Closed part) (All Regions and Country regulations) Technology transfers(API'S &Formulations), ( Paper technology & Product...
Deeply rooted in Gomti Nagar, Lucknow, Uttar Pradesh, we are an organization that renders excellent CTD and ECTD dossier preparation services to the clients at competitive charges. ECTD means an electronic common technical document that is required...
Headquartered in Gomti Nagar, Lucknow, Uttar Pradesh, we are a company that is engaged in offering dependable Drug dossier preparation services to the clients at affordable charges. For the preparation of the drug dossier, ECTD and CTD are important...
Dossiers (ctd) compilation for submissions in: asia africa middle east central america south america north america dossier compilation in common technical dossier (ctd) format and conversion to ectd for: us fda saudi fda european counties dmf (drug...
Sarims provides consulting and dossier solution for product registration. We write and review dossier as per European CTD / ASEAN CTD / non-CTD (country specific guideline). Administrative Documentation (writing and review): Registration Application...
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