[email protected] Overview of Dossier Requirements and Guidelines for Generic Product Muhammad Ali email: [email protected] ACTD: ASEAN COMMON TECHNICAL DOCUMENT AND . b) Sections of ASEAN Common technical dossier c) ACTD Guideline; 3. the discussion of existing technical guidelines and regulatory requirements;; the study of harmonised procedures and regulatory systems currently implemented.
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Common Technical Document Consists of the following Modules with the number of the. January 1, Journal article Open Access.
ASEAN Common Technical Dossier (ACTD)
Sravanthi The Regulatory Act department is very often the first point of contact between the government authorities and the company. However,applicants can modify, if needed, to provide the best possible presentation of the technical information, in order to facilitate the understanding and evaluation of the results upon pharmaceutical registration.
The drug manufacturer has to submit the drug dossier in eCTD format. Regulatory reviews and communication with the applicant is facilitated by a standard document of common elements. January 1, DOI: Once the switch to this electronic format is made it is guidelijes that further applications and responses relating to the particular medicinal product are submitted in NeeS format.
ACTD/ATR Drug Registration Requirements
This guideline merely demonstrates an appropriate write-up format for acquired data. Throughout the ACTD, the display of information should be unambiguous and transparent, in order to facilitate the review of the basic data and to help a reviewer become quickly oriented to the application contents. Different Regulatory Authority published their Standard format according to country Guidelines.
This guideline describes a CTD format that will significantly reduce the time and resources needed to compile applications for registration and in the future, will ease the yuidelines of electronic documental submissions. Asian Common Technical Documents consists of following parts.
This DOI represents all versions, and will always resolve to the latest one. A NeeS format submission can normally be yuidelines with any initial, variation or renewal MA submission.
This guideline merely demonstrates an appropriate write-up format for acquired data. ACTD format significantly reduce the time and resources needed to compile applications for registration.
The attitudes and acttd of Regulatory Affairs Professionals will condition the perceptions of the government officials to the company. Versions Version 1 You can cite all versions by using the DOI Dossier is a collection or file of documents on the same subject, especially a file containing detailed information about a person or a topic. Good for startup companies or scale up companies.
Common Pharmaceutical Dossier which is guidelins used in the Pharmaceutical Industry are: The eCTD is an interface for the pharmaceutical industry to transfer regulatory information with various regulatory agencies. All versions This version Views Downloads Data volume The Regulatory Affairs department is very often the first point of contact between the government authorities and the company.
We can provide these documents as per company requirement.