APPENDIX 9: LABELLING REQUIREMENTS
(if applicable) * NA 22. The words “Controlled Medicine/ Ubat Terkawal” (For scheduled poison only) * NA 23. Security Label (Hologram) # - NA NA : Not Applicable * Exempted for small labels (i.e. 5ml and less) used for ampoules/ cartridge, vials, eye drops, ear drops, and nose drops.
Download APPENDIX 9: LABELLING REQUIREMENTS
Information
Domain:
Source:
Link to this page:
Documents from same domain
GUIDELINE FOR STABILITY DATA
www.npra.gov.my(e.g., Efficacy of Antimicrobial Preservation of the BP or Antimicrobial Preservative Effectiveness Test of the USP) and by performing chemical assays for the preservatives during the regular stability testing schedules. If a lack of or low levels are found, testing for sterility should be carried out. iv) Dissolution testing
DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD)
www.npra.gov.myPREAMBLE This “DRUG ... *EXPLANATORY NOTES FOR REPACKERS 1. Introduction This chapter is intended to provide guidance to those engaged in repackaging of finished products with the aim to provide information to any person/ establishments who removes finished products from their original container-closure system and repackages ...
MINISTRY OF HEALTH MALAYSIA MICROBIAL …
www.npra.gov.my90ml of Buffered NaCl Peptone Solution + ≤100 cfu S. aureus Enrichment: 90ml of Tryptone Soya Broth (TSB), 30 - 35ºC, 18 – 24hrs 10 ml Selective Agar: Mannitol Salt Agar (MSA) Subculture on 30 -35ºC, 18 – 72hrs ≤100 cfu Ps. aeruginosa Cetrimide Agar (CETA)
Guidelines for Control of Cosmetic Products in Malaysia
www.npra.gov.myGUIDELINES FOR CONTROL OF COSMETIC PRODUCTS IN MALAYSIA NATIONAL PHARMACEUTICAL REGULATORY AGENCY MINISTRY OF HEALTH, MALAYSIA 1st Revision – February 2017 Please visit the NPRA website for the latest updates
Overview on ASEAN Guideline on PV Requirements
www.npra.gov.mythe effect that the same pre-approval dossier pertaining to process validation that have been submitted to the reference regulatory agency are submitted to DRA for evaluation. Under certain circumstances where validation documents may ... The …
BACTERIAL ENDOTOXIN TEST
www.npra.gov.myNPCB MOH e. Test methods • Describe how the test is performed in detail • Gel clot method: European Pharmacopeia 5.0, 2.6.14 Bacterial endotoxins, Gel clot technique (Method A and B) 1. Preparatory Testing i. Confirmation of labeled lysate sensitivity
HALAL PHARMACEUTICALS
www.npra.gov.my•The pharmaceuticals are designed and develop in a way that comply with the ... Cleaning Procedures and Validations Right Formula . NPCB 46 Validation The documented act of proving that any procedure, process, equipment, material, activity, or system actually leads to the
General Guidelines on Good Manufacturing Practices
www.npra.gov.my1.3 Good Manufacturing Practice is that part of Quality Assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the Product Registration or product specification. Good Manufacturing Practice is concerned with both production and quality control.
APPENDIX 8: LIST OF PERMITTED, PROHIBITED AND …
www.npra.gov.my32. Menthol External Preparations >16% 33. Mestranol Oral Contraceptives 34. Methylene Blue Oral Preparations 35. Midazolam All oral preparations, except 7.5mg coated tablet 36. Morphine Cough Mixtures 37. Neomycin Oral Antidiarrhoeal, Vaginal Tablets, Topical Powders, Aerosols, Nasal Preparations 38. Noradrenaline Dental Preparations 39.
Related documents
GCP INSPECTION CHECKLIST - ClinRegs
clinregs.niaid.nih.govIP Investigational Product NA not checked or not applicable PI Principal Investigator RA Regulatory Authority ... training that this could be not applicable in the case of field sites ... 3.1 Is the pharmacy access controlled, temperature and humidity
SAFETY DATA SHEET Klean Strip Paint Thinner Revision ...
content.interlinebrands.comcontainer where applicable. Large spills: Dike far ahead of spill for later disposal. Waste Disposal: Dispose in accordance with applicable local, state and federal regulations. Steps To Be Taken In Case Material Is Released Or Spilled: 7. HANDLING AND STORAGE Read carefully all cautions and directions on product label before use. Since empty ...
KX-HDV130 Operating Instructions - Panasonic North …
na.panasonic.comThis product meets the applicable Industry Canada technical specifications. Note RThis Class B digital apparatus complies with Canadian ICES-003. CAUTION Any changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate this product. Compliance with TIA-1083 standard: T ...
MATERIAL SAFETY DATA SHEET
pgproductsafety.comSECTION I - PRODUCT IDENTIFICATION ... contains all information required by the Controlled Products Regulations. Tide Pods Pg 5/5 . SECTION XVI - OTHER INFORMATION ... *N/A. - Not Applicable *N/K. – Not Known . Data supplied is for use only in connection with occupational safety and health.
Centerfire Rifle and Pistol Ammunition
www.federalpremium.comAfter the fire is controlled, heated products can still re-ignite and project pieces of metal posing risk to fire-fighters. Full PPE including respiratory protection should be worn during salvage, overhaul and fire investigation. Do not disturb the involved area until the fire is completely extinguished and the product and packaging are allowed
ANNEX A1 GUIDANCE ON PROCESS VALIDATION SCHEME …
www.hsa.gov.sgDB denotes applicable for Dry Blending only WG denotes applicable for Wet Granulation only denotes applicable (if required) NA denotes Not Applicable The product owner / applicant will determine the level of process information to be registered. Where process parameters are deemed critical but not well defined in the submission, the DRA