The electronic common technical document dossier is needed in the eCTD submissions for Pharma. MasterControl provides a solution to make this process and collection of documents easier for your company.
Pharma regulatory strategy Dossier preparation Compilation of dossier (eCTD/eDMF) Submission to regulatory authorities Product life cycle management Regulatory medical writing Regulatory guidelines consulting More Regulatory Information Management System (RIMS) ...
21DRUGS IN DEVELOPMENT DRUG PRODUCT COMPOSITIONS REF. STANDARDS OR IMPURITIES 0 EDQM 0 USP 0 JP 8 Others PATENTS & EXCLUSIVITIES 85 US Patents 0 US Exclusivities 15 Health Canada Patents DIGITAL CONTENT 3 Data Compilation #PharmaFlow 0
DATA COMPILATION #PharmaFlow NEWS #PharmaBuzz US Medicaid Prescriptions Finished Drug Prices Annual Reports APIs FDF DOSSIERS EDQM USP Others ABOUT THIS PAGE Dalteparin sodium Manufacturers ADalteparin sodium manufactureris defined as any person or entity involved in the manufacture, preparation, processing...
NEWS #PharmaBuzz US Medicaid Prescriptions Finished Drug Prices APIs FDF DOSSIERS EDQM USP Others ABOUT THIS PAGE Pethidine Manufacturers APethidine manufactureris defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pethidine, including repackag...
DATA COMPILATION #PharmaFlow APIs EXCIPIENTS ABOUT THIS PAGE STARCH API Manufacturers ASTARCH API manufactureris defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of STARCH API, including repackagers and relabelers. TheFDA regulates STARCH ...
NEWS #PharmaBuzz US Medicaid Prescriptions Finished Drug Prices Annual Reports APIs FDF DOSSIERS Patents & EXCLUSIVITIES US Patents Health Canada Patents ABOUT THIS PAGE Pirfenidone Manufacturers APirfenidone manufactureris defined as any person or entity involved in the manufacture, preparation, processing...
AEdurant manufactureris defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edurant, including repackagers and relabelers. TheFDA regulates Edurant manufacturersto ensure that their products comply with relevant laws and regulations and are ...
AMucaine manufactureris defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mucaine, including repackagers and relabelers. TheFDA regulates Mucaine manufacturersto ensure that their products comply with relevant laws and regulations and are...
0 DRUGS IN DEVELOPMENT DRUG PRODUCT COMPOSITIONS REF. STANDARDS OR IMPURITIES 0 EDQM 0 USP 0 JP 2 Others PATENTS & EXCLUSIVITIES 0 US Patents 0 US Exclusivities 0 Health Canada Patents DIGITAL CONTENT 0 Data Compilation #PharmaFlow 0