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DRAFT 5 APPENDIX 13: DRUG MASTER FILES AND CERTIFICATES OF SUITABILITY 1. GENERAL OVERVIEW 1.1. Who should submit the document? The applicant of the product registration shall submit the DMF or the
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Individuals or businesses seeking to obtain certification or approval from SIRIM (Standard and Industrial Research Institute of Malaysia).
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mys17-text - sirim is a form required by SIRIM (Standards and Industrial Research Institute of Malaysia) for reporting specific information.
Certain companies and manufacturers in Malaysia are required to file mys17-text - sirim.
mys17-text - sirim can be filled out electronically on the SIRIM website or manually by submitting a physical form.
The purpose of mys17-text - sirim is to ensure compliance with regulations and standards set by SIRIM.
Information such as product details, manufacturing processes, materials used, and quality control measures must be reported on mys17-text - sirim.
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