ACTD GUIDELINES PDF
[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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You can cite all versions by using the DOI This guideline merely demonstrates an appropriate write-up format for acquired data.
ACTD/ATR Drug Registration Requirements
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. Common Technical Document Consists of the following Modules with the number of the. January 1, Journal article Open Access. The attitudes and actions of Regulatory Affairs Professionals will condition the perceptions of the government officials to the company.
January 1, DOI: Common Pharmaceutical Dossier which is widely used in the Pharmaceutical Industry are: Versions Version 1 Dossier is a collection or file of documents on the same subject, especially a file containing detailed information about a person or a topic.
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 preparation of electronic documental submissions. This DOI represents all versions, and will always resolve to the latest one.
ACTD format significantly reduce the time and resources needed to compile applications for registration. The guudelines manufacturer has to submit the drug dossier in eCTD format. The eCTD is an interface for the pharmaceutical industry to transfer regulatory information with various regulatory agencies.
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 Regulatory Affairs department is very often the first point of contact between the government authorities and the company.
Once the switch to this electronic guidelinse is made it is expected that further applications and responses relating to the particular medicinal product are submitted in NeeS format. Sravanthi The Regulatory Affairs department is very often the first point of contact between the government authorities and the company. This guideline merely demonstrates an appropriate write-up format for acquired data. All versions This version Views Downloads Data volume Good for startup companies or scale up companies.
Different Regulatory Authority published their Standard format according to country Guidelines.
Regulatory reviews and communication with the applicant is facilitated by a standard document of common elements. A NeeS format submission can normally be started with any initial, variation or renewal MA submission. We can provide these documents as per company requirement. Asian Common Technical Documents consists of following parts.