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  • USP Monographs: Glutaral Concentrate

    2014-9-5 · » Glutaral Concentrate is a solution of glutaraldehyde in Purified Water. It contains not less than 100.0 percent and not more than 104.0 percent of the labeled amount, the labeled amount being 50.0 g of C 5 H 8 O 2 per 100 g of Concentrate.

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  • NF Monographs: Glutaral Disinfectant Solution

    2014-9-5 · Standard preparation— Transfer an accurately weighed quantity of Glutaral Concentrate, previously assayed as directed in the Assay under Glutaral Concentrate, equivalent to about 2.5 g of glutaraldehyde, to a 100-mL volumetric flask, dilute with water to volume, and mix. Dilute an accurately measured volume of this solution quantitatively and stepwise with water to …

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  • General Information <1121> Nomenclature - USP–NF

    2011-10-7 · Glutaral Concentrate (used to prepare Glutaral Disinfectant Solution) For products intended for parenteral administration, the use of the word ‘‘Concentrate’’ in the monograph title is restricted to one specific monograph, Potassium Chloride for Injection Concentrate. The word ‘‘Concentrate’’ should not appear in the monograph title

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  • <1121> NOMENCLATURE - DrugFuture

    Glutaral Concentrate (used to prepare Glutaral Disinfectant Solution) For products intended for parenteral administration, the use of the word “Concentrate” in the monograph title is restricted to one specific monograph, Potassium Chloride for Injection Concentrate.

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  • USP29-NF24

    2221 USP Monographs: Glutamine. 2222 USP Monographs: Glutaral Concentrate. 2223 NF Monographs: Glutaral Disinfectant Solution. 2224 USP Monographs: Glyburide. 2225 USP Monographs: Glyburide Tablets. 2226 USP Monographs: Glycerin.

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  • This document is referenced in USP General Chapter <1121 ...

    2020-8-5 · This document is referenced in USP General Chapter <1121> ... Guideline for Assigning Titles to USP Dietary Supplements Monographs, which is also used as a basis for decisions by the Nomenclature and ... Concentrate (used to prepare Isosorbide Oral Solution) and Glutaral Concentrate (used to prepare Glutaral Disinfectant Solution).

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  • USP

    2017-6-29 · chemical medicines monographs 2 ticlopidine hydrochloride tablets tiletamine and zolazepam for injection ... glutaral concentrate glutaral disinfectant solution glutethimide glutethimide capsules glutethimide tablets ... general notices to usp-nf volumetric solutions <1230> water for hemodialysis applications

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  • Nomenclature Guideline Outline - USP–NF | USP-NF

    2018-2-1 · “Concentrate” nomenclature Some drug substances are available as concentrated solutions or mixture of solids (dispersions), and are intended to be used as intermediates for final formulations, e.g., Isosorbide Concentrate (used to prepare Isosorbide Oral Solution), and Glutaral Concentrate (used to prepare Glutaral Disinfectant Solution).

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  • Accessed from 128.83.63.20 by nEwp0rt1 on Tue Nov 29 21:45 ...

    2011-11-30 · 4 ·HCl 183.59 tity of Glutaral Concentrate, previously assayed as directed in L-2-Aminoglutaric acid, hydrochloride; the Assay under Glutaral Concentrate, equivalent to about 2.5 g 2-Aminopentanedioic acid, hydrochloride [138-15-8]. of glutaraldehyde, to a 100-mL volumetric flask, dilute with DEFINITION water to volume, and mix. Dilute an accurately measured vol-

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  • FCSD Chemicals and Lubricants

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  • Hand sanitizer information for compounders - USP

    2021-5-21 · WHO. The WHO provides a practical guide for use at the pharmacy bench during the actual preparation of the hand sanitizer formulations. Information in the guide includes materials required for small volume production and 10-liter preparations. Formulations include starting material of ethanol 96% for final product concentration of ethanol 80% (v/v) or starting material …

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  • Pharmaceutical Water Treatment | Systems & Services ...

    Water is one of the major commodities used by the pharmaceutical industry. It is widely used as a raw material, ingredient and solvent in the processing, formulation and manufacture of pharmaceutical products, active pharmaceutical ingredients (API’s) and intermediates, and analytical reagents.

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  • The Regulated Dietary Supplement Industry: Myths of an ...

    2021-2-6 · Compendial standards established by USP have legal effect under the FDCA and are enforceable by FDA. Under the DSHEA amendments to the FDCA, a dietary supplement will be deemed misbranded if it is falsely represented as conforming to the specifications of an official compendium (such as USP monographs). 43. In 1995, USP members adopted a ...

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  • according to 29 CFR 1910.1200 and GHS Page 1/10 Companion™

    2019-5-23 · Monographs, Volumes 1-112. Reproductive toxicity No data available. STOT-single exposure Inhalation may cause coughing, tightness of the chest and irritation of the respiratory system. STOT-repeated exposureNo data available. Aspiration hazard No data available. Repeated or prolonged exposure Avoid prolonged or repeated exposure.

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  • Purified Water - Pharmaceutical Guidance

    2020-8-17 · Purified Water systems must be validated. Purified Water systems that produce,store,and circulate water under ambient conditions are susceptible to the establishment of tenacious biofilms of microorganisms,which can be the source of undesirable levels of viable microorganisms or endotoxins in the effluent water.

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  • FIR No. CASRN Designated List(s) Link to the Ford US SDS

    2019-12-11 · Glutaral 111-30-8 Component of Surfactant 8, 20 Cyclotetrasiloxane 556-67-2 Component of Antifoam 6, 7, 21 Sulfuric acid 7664-93-9 Component of Surfactant 9,15, 20

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  • Albuterol Monograph for Professionals - Drugs.com

    2021-5-9 · Aldehydes Stephen A. Kelly Sean P. Gorman Brendan F. Gilmore Aldehydes (from the Latin alcohol dehydrogenatum, alcohol deprived of hydrogen) are compounds containing the functional group—CHO formed as a result of oxidation of primary alcohols, where the carbonyl group is bonded to at least one hydrogen atom. The general formula for an aldehyde and the…

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  • Aldehydes | Basicmedical Key

    USP-NF is a combination of two compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). Monographs for drug substances, dosage forms, and compounded preparations are featured in the USP. Monographs for dietary supplements and ingredients appear in a separate section of the USP. Excipient monographs are in the NF 27.01.

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  • 3.2 TEST FOR STERILITY - WHO

    Japanese Pharmacopoeia (JP) and United States Pharmacopeia (USP). This internationally harmonized test replaces the current method 3.2.1 Test for sterility of non-injectable preparations and 3.2.2 Sterility testing of antibiotics. As a consequence, all references to 3.2.1 and 3.2.2 in Ph.Int. monographs will be changed.

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  • The Regulated Dietary Supplement Industry: Myths of an ...

    2021-2-6 · Compendial standards established by USP have legal effect under the FDCA and are enforceable by FDA. Under the DSHEA amendments to the FDCA, a dietary supplement will be deemed misbranded if it is falsely represented as conforming to the specifications of an official compendium (such as USP monographs). 43. In 1995, USP members adopted a ...

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  • USP 31 General Information h1121i Nomenclature | Topical ...

    2014-3-29 · 1121 Nomenclature - Free download as PDF File (.pdf), Text File (.txt) or read online for free. 1121 Nomenclature

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  • guide to master formulae final 2012 - WHO

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  • Material Safety Data Sheet U.S. Department of Labor

    2017-11-14 · ST. Gabriel Organics BurnOut II Concentrate Active ingredient: Clove Oil 18%, Citric Acid 30% Inert ingredients: Mineral oil, (USP), Water, Gum Arabic Total other 52% Total 100% Note: Blank spaces are not permitted. If any item is not applicable, or no information is available, the space must be marked to indicate this. Section I

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  • Usp34 Nf29 Index | Assay | Calcium - Scribd

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  • Formulations | Cadila Pharmaceuticals

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  • (PDF) Handbook of Analytical Techniques, 2 Volume

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  • USP - als alleinstellungsmerkmal ( englisch unique selling ...

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  • 3.2 TEST FOR STERILITY - WHO

    Japanese Pharmacopoeia (JP) and United States Pharmacopeia (USP). This internationally harmonized test replaces the current method 3.2.1 Test for sterility of non-injectable preparations and 3.2.2 Sterility testing of antibiotics. As a consequence, all references to 3.2.1 and 3.2.2 in Ph.Int. monographs will be changed.

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  • Ashland | Products

    Guide to Master Formulae Guidance Document 1 This guidance document GUIDE TO MASTER FORMULAE is one of a series developed by WHO/FWC/IVB Quality, Safety & Standards team upon request from the manufacturers’ members of the Developing Countries …

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  • guide to master formulae final 2012 - WHO

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  • Our Products | Pfizer Canada

    2021-1-15 · Factor IX (human) and factor IX complex (human) are prepared from pooled human plasma; different methods (e.g., murine monoclonal antibody, chromatography, nanofiltration) are used to isolate and purify factor IX. Undergoes viral inactivation processes (e.g., heat, solvent/detergent) to reduce risk of viral transmission.

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  • Factor IX (Human), Factor IX Complex (Human) - Drugs

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  • (PDF) INDIAN PHARMACOPOEIA 2007 Volume 1 | Sai

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  • Drug Register - National Drug Authority

    In the final monographs, Health Canada approved the oral use of aloe latex as a stimulant laxative for relief of occasional constipation 8 and the topical use of the leaf gel to help relieve minor burns including sunburn and to assist healing of minor wounds such as cuts, burns, and minor skin irritations. 9 In the United States, aloe was ...

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  • Aloe - American Botanical Council

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  • APVMA Risk Assessment Manual

    2018-4-25 · If the method of analysis is a compendial method (BP, EP, USP) or CIPAC method, the APVMA will forward the relevant methodology to the analytical laboratory. In this instance a reduced validation may be required to ensure that the analytical laboratory is …

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  • TMEP Chapter 1200

    2021-2-19 · Chapter 1200. Substantive Examination of Applications. 1201 Ownership of Mark 1201.01 Claim of Ownership May Be Based on Use By Related Companies 1201.02 Identifying the Applicant in the Application 1201.02(a) Identifying the Applicant Properly 1201.02(b) Application Void if Wrong Party Identified as the Applicant 1201.02(c) Correcting Errors in How the Applicant …

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  • Printing Processes and Printing Inks - Printing Processes ...

    The origins of printing can be traced back several centuries. Pictorial prints were produced from cut wood blocks in Japan during the tenth century and probably earlier in China. The first movable type, moulded in clay, can be traced to China in the eleventh century, and wooden type appeared in China in the fourteenth century. In Europe, book production from wood blocks was seen early in …

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  • Journal of Radiological Protection, Volume 21, Number 2 ...

    In his early years in the Factory Inspectorate, Peter was involved in enforcement of the 1961 Sealed Sources Regulations and the formulation, as well as subsequent enforcement, of the 1968 Unsealed Radioactive Substances and 1969 Sealed Sources Regulations.

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    37 Full PDFs related to this paper. READ PAPER. 44091608-Pharmaceutical-Coating-Technol

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  • Analytical Chemist Resume Samples | Velvet Jobs

    2013-4-27 · Pharmaceutical Wate112 - Free download as Word Doc (.doc .docx), PDF File (.pdf), Text File (.txt) or read online for free. Purified Water for Pharmaceutical uses are tested according USP BP/EP or IP

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  • TMEP Chapter 1200

    2021-2-19 · Chapter 1200. Substantive Examination of Applications. 1201 Ownership of Mark 1201.01 Claim of Ownership May Be Based on Use By Related Companies 1201.02 Identifying the Applicant in the Application 1201.02(a) Identifying the Applicant Properly 1201.02(b) Application Void if Wrong Party Identified as the Applicant 1201.02(c) Correcting Errors in How the Applicant …

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  • Register with FDA | Registrar

    To register with the United States FDA, click 'Previous' and select 'United States FDA.' You indicated that your facility handles . A Regulatory Advisor will contact you for more information about these products. You Indicated that your facility …

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  • Gattefossé | Ingrédients cosmétiques & excipients ...

    Fournisseur d'ingrédients cosmétiques et d'excipients pharmaceutiques, Gattefossé explore ce que la nature et la science ont de meilleur depuis1880.

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  • 1231 Water for Pharmaceutical Purposes Usp35 | Purified ...

    2018-11-30 · The Water for Hemodialysis monograph includes total aero- bic microbial count (TAMC) limits of 100 cfu/mL and endo- toxin limits of 1 USP Endotoxin Unit/mL. In addition, the absence of Pseudomonas aeruginosa should be routinely de- termined because this is an opportunistic pathogen hazard- ous to acutely ill hemodialysis patients. Both the high mi- crobial …

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  • Speakers | Food Safety Summit SA

    He participated in International Agency for Research on Cancer Monographs 56 and 86, and a panel leading to an IARC publication on mycotoxins and public health (Scientific Publication 158). He was a member of the drafting committee of the World Health Organization IPCS …

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  • FORMALDEHYDE CASRN 50-00-0 - Lindane

    2020-1-16 · Formaldehyde is one of the volatile compounds formed in the early stages of decomposition of plant residues in the soil (1). Formaldehyde occurs naturally in fruits and other foods (1). Other sources are forest fires, animal wastes, microbial products of biological systems, and plant volatiles (2,3).

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  • My Pharma Blog: July 2016

    2016-7-24 · PROCEDURE. 1. Prepare 0.9% saline solution and dispense 10 ml quantity in test tube and put one sterile cotton swab in it and sterilize in autoclave at 15 lbs pressure and 121°C for 15 minutes or use pre sterilized swab tubes and fill with 10 ml sterile 0.9% saline solution. 2.

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  • Speakers | Food Safety Summit SA

    He participated in International Agency for Research on Cancer Monographs 56 and 86, and a panel leading to an IARC publication on mycotoxins and public health (Scientific Publication 158). He was a member of the drafting committee of the World Health Organization IPCS …

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  • Register with FDA | Registrar

    To register with the United States FDA, click 'Previous' and select 'United States FDA.' You indicated that your facility handles . A Regulatory Advisor will contact you for more information about these products. You Indicated that your facility …

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  • #739 COLON Clear Cleanse Formula Natural Detox

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  • My Pharma Blog: July 2016

    2016-7-24 · PROCEDURE. 1. Prepare 0.9% saline solution and dispense 10 ml quantity in test tube and put one sterile cotton swab in it and sterilize in autoclave at 15 lbs pressure and 121°C for 15 minutes or use pre sterilized swab tubes and fill with 10 ml sterile 0.9% saline solution. 2.

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  • US6335365B1 - Fireproof, non-exploding nitroglycerine

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    2021-2-9 · Monographs. 1. Alexander, R. (1995), “Security, women, and tuna: a look at Fiji”, in Fishing for answers: women and fisheries in the Pacific islands, edited by Elizabeth Matthews for the Women and Fisheries Network, Oceania Printers Ltd, Suva (Fiji): 91-100. The paper offers a model to approach security, women and tuna and goes through the description of two local industries, a …

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    Fournisseur d'ingrédients cosmétiques et d'excipients pharmaceutiques, Gattefossé explore ce que la nature et la science ont de meilleur depuis1880.

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  • DDT (PIM 127) - INCHEM

    2020-12-10 · DDT is a central nervous system stimulant, acting chiefly on the cerebellum and motor cortex. The liver is the only other organ significantly affected by DDT. 2.2 Summary of clinical effects The earliest symptom of poisoning by DDT is hyperaesthesia of the mouth and lower part of …

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  • Pharmacy Practice and the Law Exam 1 Flashcards | Quizlet

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  • FDA Regulatory Affairs | Pisano, Douglas J. | download

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  • Selected Medicinal Plant

    2021-3-6 · Following extensive discussion, 31 of the 33 draft monographs were adopted for inclusion. At the subsequent tenth International Conference of Drug Regulatory Authorities held in China, Hong Kong Special Administrative Region in June 2002, the 31 draft monographs adopted for volume 3 of the WHO monographs on selected medicinal plants were presented.

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    1994-1-3 · (5) The threshold check solution consists of 0.83 grams of sodium saccharin USP in 1 cc of warm water. It can be prepared by putting 1 cc of the fit test solution (see (b)(5) below) in 100 cc of distilled water.

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  • Medical Glove Guidance Manual - Latex Allergy Info

    1999-7-30 · The USP-NF is a standards setting body in the United States. The USP-NF is officially recognized in the Federal Food, Drug and Cosmetic Act (Act). Under section 502(g) of the Act, if a product is claimed to be the same as one named in an official compendium, including the USP-NF, it must be packaged and labeled in accordance with the ...

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  • Selected Medicinal Plant

    2021-3-6 · Following extensive discussion, 31 of the 33 draft monographs were adopted for inclusion. At the subsequent tenth International Conference of Drug Regulatory Authorities held in China, Hong Kong Special Administrative Region in June 2002, the 31 draft monographs adopted for volume 3 of the WHO monographs on selected medicinal plants were presented.

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  • Hopi | Encyclopedia.com

    2018-6-11 · An undergarment factory was established in Winslow, Arizona, in partnership with the Hopis in 1971 but failed in only a few years. By the late twentieth century, the Hopis had a diverse economy of small-scale farming and livestock grazing, various small businesses, mineral development royalty payments, government subsidies for community ...

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  • Pharmaceutical Coating Technol | Tablet (Pharmacy) |

    2021-5-7 · Table 2.2 shows that the USP and JP recognize definite substitution types in separate monographs. The first two digits of the four-digit designation specify the nominal percentage of methoxyl groups while the final two specify the nominal. Fig. …

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  • EUCALYPTUS ONLINE BOOK

    2021-1-22 · Ultimately, our Eucalyptus Newsletter is also oriented to offer, free-of-charge and to all interested people, the 'Eucalyptus Online Book' chapters, launched as a digital book about the many aspects of the Eucalyptus , totally written by Celso Foelkel. We invite you all to visit our 2005/2011 archives and to access our technical production ...

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  • Pharmacy News Online: LIST OF PHARMACEUTICAL

    2013-1-25 · Aboseldehyde limited Address: Plot C20, LSDPC Amuwo Odofin Scheme, Commercial Layout, Apapa/Oshodi E/Way, Lagos. Phone: +234 1 496 7251, 493 1811; Fax: +234 1 967 251 Afrab-Chem Limited Address: 22, Abimbola Street, Isolo Industrial Estate, Isolo, Lagos. Phone: +234 1 452 2571, 452 2777;

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  • BNNK Tana Toraja Rakor Pelaksanaan Penguatan ...

    2020-9-15 · TODAY, MAKALE – BNNK Tana Toraja mengikuti kegiatan Rapat Koordinasi Pelaksanaan Penguatan Ketahanan Keluarga Berbasis Sumber Daya Pembangunan Desa secara virtual, Selasa 15 September 2020. Rapat koordinasi diikuti Kepala BNNK Tana Toraja AKBP Natalya Dewi, Plt Kasi P2M Juanedi Bara’padang dan juga melibatkan Dinas DPML, Lembang Ratte …

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