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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This guideline describes a CTD guirelines 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.

REGULATORY DOSSIER- ASEAN COMMON TECHNICAL DOCUMENT (ACTD) FOR ASEM COUNTRIES

Different Regulatory Authority published their Standard format according to country Guidelines. Dossier is a collection or file of documents on the same subject, especially a file containing detailed information about a person or a topic.

Common Pharmaceutical Dossier which is widely used in the Pharmaceutical Industry are: The drug manufacturer has to submit the drug dossier in eCTD format. ACTD format significantly reduce the acts and resources needed to compile applications for registration.

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We can provide these documents as per company requirement. Guidellnes 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. January 1, DOI: Good for startup companies or scale up companies.

Regulatory reviews and communication with the applicant is facilitated guiedlines a standard document of common elements.

A NeeS format submission can normally be started with any initial, variation or renewal MA submission. All versions This version Views Downloads Data volume You can cite all versions by using the DOI January 1, Journal article Open Access.

The eCTD is an interface for the pharmaceutical industry to transfer regulatory information with various regulatory agencies. The attitudes and actions of Regulatory Affairs Professionals will condition the perceptions of the government officials to the company.

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Once the switch to this electronic format is made it is expected that further applications and responses relating to the particular medicinal product are submitted in NeeS format.

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This guideline merely demonstrates an appropriate write-up format for acquired data. This DOI represents all versions, and will always resolve to the latest one. 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. Common Technical Document Consists of the following Modules with the number of the.

Versions Version 1 The Regulatory Affairs department is very often the first point of contact between the government authorities and the company. 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 gudielines reviewer become quickly oriented to the application contents.

Asian Common Technical Documents consists of following parts.