KAY RELEASE AGENT

Informasi Utama

  • Nama dagang:
  • KAY RELEASE AGENT
  • Digunakan untuk:
  • manusia
  • Jenis Obat:
  • Perangkat medis

Dokumen

  • untuk masyarakat umum:
  • Informasi leaflet untuk produk ini saat ini tidak tersedia, Anda dapat mengirim permintaan untuk layanan pelanggan kami dan kami akan memberitahu Anda segera setelah kami mampu mendapatkannya.


    Meminta selebaran informasi untuk masyarakat umum.

Lokalisasi

  • Tersedia di:
  • KAY RELEASE AGENT
    Indonesia
  • Bahasa:
  • Bahasa Indonesia

Informasi lainnya

Status

  • Sumber:
  • Ecolab
  • Nomor Otorisasi:
  • 911803-02
  • Pembaharuan Terakhir:
  • 12-03-2018

Ringkasan karakteristik Produk: dosis, interaksi, efek samping

LEMBAR DATA KESELAMATAN BAHAN KIMIA

Keterangan Dasar Halaman 1

dari 5 halaman Tanggal

Dibuat: 24 Juli 2007

BAGIAN 1 : PRODUK BAHAN KIMIA DAN IDENTIFIKASI PERUSAHAAN

1.1

Keterangan Produk

Nama produk :

KAY

RELEASE AGENT

Kegunaan :

Larutan pembersih

Jenis produk :

Larutan

1.2 Identifikasi Perusahaan

Nama dan alamat pabrik pembuat :

Kay Chemical Company

8300 Capital Drive

Greensboro, NC 27409

1-800-529-5458 (Layanan Pelanggan)

Nama dan alamat importir/distributor

PT. ECOLAB INDONESIA

Mid Plaza II, Lantai 7

Jl. Jend. Sudirman Kav. 10-11

Jakarta 10220

Indonesia

Nomor telpon darurat :

(1) Sambungan bebas pulsa dari Indonesia

(Pusat Pemantauan Racun Amerika Serikat)

1.3 Kontak Tujuan

Jika terjadi keracunan, hubungi 001-803-011-3848

Jika tersambung, tekan "5"

Beritahu penjawab “Kay Chemical Company” dari

negara mana Anda menelpon.

Tunggu untuk penerjemah bahasa (bilamana perlu).

(2) Collect calling (biaya dibebankan ke penerima telpon)

(001) 303-592-1709

Jabatan :

Field Service Manager

Nomor telpon :

+(603) 5891-1857

BAGIAN 2 : KOMPOSISI / INFORMASI BAHAN

Bahan/preparat :

Preparat

Produk ini tidak mengandung bahan atau bahan tambahan yang, sepengetahuan pemasok dan dalam kadar yang dapat

diterapkan, tergolong sebagai bahan yang berbahaya bagi kesehatan atau lingkungan sehingga perlu dilaporkan pada

bagian ini.

Batas(batas) pemajanan di tempat kerja, jika ada, tercantum pada bagian 9.

* Informasi toksikologis, jika ada, tercantum pada bagian 11.

Produk :

KAY

RELEASE AGENT

Halaman 2 dari 5 halaman

BAGIAN 3: SIFAT FISIKA DAN KIMIA

Informasi umum

Tampilan

Bentuk fisik :

Cairan

Warna :

Putih

Bau :

Tidak berbau

Informasi penting berkaitan dengan kesehatan, keselamatan dan lingkungan

pH :

Titik nyala :

> 93,3°C (cawan tertutup)

Kepadatan relatif :

0,995 (air = 1)

Daya larut :

Mudah larut dalam bahan-bahan berikut: air dingin dan air panas.

BAGIAN 4 : IDENTIFIKASI BAHAYA

Preparat ini tidak tergolong berbahaya menurut Petunjuk 1999/45/EC dan amandemennya.

Penggolongan :

Tidak digolongkan

Lihat bagian 11 untuk informasi lebih terperinci tentang pengaruh pada kesehatan dan gejala kesehatan.

BAGIAN 5 : LANGKAH-LANGKAH PERTOLONGAN PERTAMA

Terhirup :

Jika terhirup, pindahkan ke tempat berudara segar. Cari pertolongan medis jika

timbul gejala.

Tertelan :

Berkumurlah dengan air. Jangan dipaksa untuk dimuntahkan kecuali atas petunjuk

petugas medis. Jika muntah, bungkukkan kepala sehingga cairan muntahan tidak

memasuki paru-paru. Cari pertolongan medis jika timbul gejala.

Terkena kulit :

Basuh kulit yang terkena dengan air dalam jumlah banyak. Lepaskan pakaian dan

sepatu yang terkontaminasi. Cari pertolongan medis jika timbul gejala.

Terkena mata :

Jika terkena mata, segera basuh dengan air dalam jumlah banyak. Cari pertolongan

medis jika terjadi iritasi.

BAGIAN 6 : TINDAKAN PENANGGULANGAN KEBAKARAN

Titik nyala :

>93,3°C (cawan tertutup)

Bahan pemadam :

Sesuai :

Gunakan bahan pemadam yang sesuai untuk api yang menjalar.

Tidak sesuai :

Tidak diketahui

Bahaya khusus :

Tidak ada bahaya tertentu.

Produk berbahaya penyebab :

Produk pengurai mungkin termasuk bahan berikut: karbon oksida.

kebakaran

BAGIAN 7 : TINDAKAN MENGATASI KEBOCORAN DAN TUMPAH

Pencegahan diri :

Tidak diperlukan tindakan khusus.

Pencegahan lingkungan :

Ceceran bahan jangan sampai menyebar , mengalir ke dalam dan jatuh ke

tanah, saluran air, pipa pembuangan dan pipa riol.

Produk :

KAY

RELEASE AGENT

Halaman 3 dari 5 halaman

cecer :

Untuk ceceran, taburkan bahan penyerap di atasnya (jika tidak tersedia bahan

penyerap yang sesuai dapat menggunakan tanah), serok lalu masukkan ke

dalam wadah tahan-cairan yang dapat disegel untuk dibuang.

Catatan: lihat bagian 9 untuk peralatan perlindungan diri dan bagian 13 untuk pembuangan limbah.

BAGIAN 8 : PENANGANAN DAN PENYIMPANAN

Penanganan :

Cuci bersih setelah penanganan.

Penyimpanan :

Simpan wadah dalam keadaan tertutup rapat. Simpan wadah di dalam ruangan

yang sejuk dan berventilasi baik.

Bahan kemasan

Penggunaan yang dianjurkan:

Gunakan wadah asli.

BAGIAN 9 : PENGENDALIAN PEMAJANAN DAN ALAT PERLINDUNGAN DIRI

Nilai batas pemajanan :

Tidak tersedia

Pengendalian pemajanan

Pelindung pernapasan:

Tidak diperlukan respirator selama digunakan secara normal dan sesuai dengan

tujuan penggunaan produk.

Pelindung tangan:

Tidak diperlukan pelindung khusus.

Pelindung mata:

Tidak diperlukan pelindung mata

Pelindung kulit:

Tidak diperlukan pakaian pelindung khusus.

BAGIAN 10 : STABILITAS DAN REAKTIFITAS

Stabilitas:

Produk ini stabil. Selama disimpan dan digunakan dalam kondisi normal, tidak

akan terjadi polimerisasi berbahaya.

Kondisi yang harus dihindari:

Tidak ada data tertentu.

Bahan yang harus dihindari:

Tidak ada data tertentu.

BAGIAN 11 : INFORMASI TOKSIKOLOGI

Pengaruh kesehatan akut yang mungkin terjadi

Terhirup :

Pengaruh signifikan atau bahaya kritis tidak diketahui.

Tertelan :

Pengaruh signifikan atau bahaya kritis tidak diketahui

Terkena kulit :

Pengaruh signifikan atau bahaya kritis tidak diketahui

Terkena mata :

Pengaruh signifikan atau bahaya kritis tidak diketahui

Toksisitas akut

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

Pengaruh kesehatan kronik yang mungkin terjadi

Toksisitas kronis

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

Karsinogenisitas

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

Produk :

KAY

RELEASE AGENT

Halaman 4 dari 5 halaman

Mutagenisitas

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

Teratogenisitas

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

Toksisitas Reproduktif

Kesimpulan/Ringkasan:

Pengaruh signifikan atau bahaya kritis tidak diketahui

BAGIAN 12 : INFORMASI EKOLOGI

Pengaruh lingkungan :

Pengaruh signifikan atau bahaya kritis tidak diketahui

Ekotoksisitas akuatik

Kesimpulan/Ringkasan:

Tidak tersedia.

Informasi ekologis lain

Biodegradabilitas

Kesimpulan/Ringkasan:

Tidak tersedia.

Pengaruh merugikan lain:

Pengaruh signifikan atau bahaya kritis tidak diketahui

BAGIAN 13 : INFORMASI PEMBUANGAN

Limbah harus dibuang sesuai dengan peraturan pengawasan lingkungan di tingkat daerah, provinsi dan negara.

Metode pembuangan:

Ceceran bahan jangan sampai menyebar , mengalir ke dalam dan jatuh ke

tanah, saluran air, pipa pembuangan dan pipa riol.

BAGIAN 14 : INFORMASI PENGANGKUTAN

Informasi

Peraturan

Nomor UN

Nama Pengangkutan

yang Tepat

Penggolongan

Label

Informasi

Tambahan

Gol ADR/RID

Tidak diatur

Gol IMDG

Tidak diatur

Gol IATA-DGR

Tidak diatur

KK* : Kelompok Kemasan

BAGIAN 15 : INFORMASI PERATURAN

Peraturan EU

Frasa risiko :

Produk ini tidak tergolong berbahaya menurut undang-undang EU.

Kegunaan produk :

Digunakan di industri

Peraturan EU lain

Frasa peringatan tambahan:

Lembar Data Keselamatan tersedia untuk pengguna kalangan profesional

berdasarkan permintaan.

Produk :

KAY

RELEASE AGENT

Halaman 5 dari 5 halaman

BAGIAN 16 : INFORMASI LAIN

Sejarah

Tanggal dicetak:

24 Juli 2007

Tanggal diterbitkan:

24 Juli 2007

Tanggal terbitan sebelumnya:

Tidak ada pengesahan sebelumnya.

Versi:

Menandakan informasi yang telah berubah dari versi terbitan sebelumnya.

Sepengetahuan kami, informasi yang dimuat di sini adalah akurat. Namun, pemasok di atas maupun cabang-

cabangnya tidak bertanggung jawab atas keakuratan atau kelengkapan informasi yang dimuat di sini.

Penentuan terakhir tentang kesesuaian setiap bahan merupakan tanggung jawab pengguna sepenuhnya. Semua bahan

mungkin dapat menimbulkan bahaya yang tidak diketahui dan harus digunakan secara hati-hati. Walaupun bahaya

tertentu telah dijelaskan di sini, kami tidak dapat menjamin bahwa hanya bahaya inilah yang akan timbul.

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FDA Releases Annual Summary Report on Antimicrobials Sold or Distributed in 2017 for Use in Food-Producing Animals Showing Declines for Past Two Years

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26-11-2018

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16-11-2018

FDA Proposes Study with Intent of Eliminating Use of Dogs in Certain Types of Research

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15-11-2018

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6-11-2018

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31-10-2018

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30-10-2018

FDA Announces Plant and Animal Biotechnology Innovation Action Plan

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23-10-2018

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18-10-2018

CTG recalls Friction Powered School Bus

CTG recalls Friction Powered School Bus

Health Canada's sampling and evaluation program has determined that the school bus toy does not meet Canadian safety requirements for toys. Specifically, the school bus released small parts during testing, which are a choking hazard for young children.

Health Canada

17-10-2018

Pest categorisation of Stagonosporopsis andigena

Pest categorisation of Stagonosporopsis andigena

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of Stagonosporopsis andigena, the causal agent of black blight of potato, for the EU. The pest is a well‐defined fungal species and reliable methods exist for its detection and identification. S. andigena is present in Bolivia and Peru. The pest is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC as Phoma andina, meaning its introduction into the EU is prohibited. The ma...

Europe - EFSA - European Food Safety Authority Publications

17-10-2018

Pest categorisation of Thecaphora solani

Pest categorisation of Thecaphora solani

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of the fungus Thecaphora solani, the causal agent of smut of potato, for the EU. The identity of the pest is well established and reliable methods exist for its detection and identification. T. solaniis present in Bolivia, Chile, Colombia, Ecuador, Mexico, Panama, Peru and Venezuela. The pathogen is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC, meaning its introducti...

Europe - EFSA - European Food Safety Authority Publications

16-10-2018

Brexit: Two-year implementation period for name and address changes

Brexit: Two-year implementation period for name and address changes

During an implementation period of maximum two years, it will be permitted to sell released packs on which a UK marketing authorisation holder or a representative is indicted as well as packs on which an EEA marketing authorisation holder or a representative is indicated for the concerned D.Sp.No. (Danish speciality number).

Danish Medicines Agency

16-10-2018

Pest categorisation of Melampsora farlowii

Pest categorisation of Melampsora farlowii

Published on: Mon, 15 Oct 2018 00:00:00 +0200 Following a request from the European Commission, the EFSA Panel on Plant Health performed a pest categorisation of Melampsora farlowii, a well‐defined and distinguishable fungus of the family Melampsoraceae. M. farlowii is the causal agent of a leaf and twig rust of hemlocks (Tsuga spp.) in eastern North America. The pathogen is regulated in Council Directive 2000/29/EC (Annex IAI) as a harmful organism whose introduction into the EU is banned. M. farlowii ...

Europe - EFSA - European Food Safety Authority Publications

9-10-2018

MDV Sports Canada recalls Marker Kingpin Ski bindings

MDV Sports Canada recalls Marker Kingpin Ski bindings

These bindings are being recalled because a pin in the toe piece can break, resulting in reduced release/retention posing a fall hazard.

Health Canada

18-9-2018

FDA takes important steps to encourage appropriate and rational prescribing of opioids through final approval of new safety measures governing the use of immediate-release opioid analgesic medications

FDA takes important steps to encourage appropriate and rational prescribing of opioids through final approval of new safety measures governing the use of immediate-release opioid analgesic medications

FDA takes important steps to encourage appropriate and rational prescribing of opioids through final approval of new safety measures governing the use of immediate-release opioid analgesic medications.

FDA - U.S. Food and Drug Administration

14-9-2018

FDA Releases Five-Year Plan for Supporting Antimicrobial Stewardship in Veterinary Settings

FDA Releases Five-Year Plan for Supporting Antimicrobial Stewardship in Veterinary Settings

CVM’s five-year action plan for supporting antimicrobial stewardship in veterinary settings builds upon the important steps CVM has taken to eliminate production uses of medically important antimicrobials.

FDA - U.S. Food and Drug Administration

13-9-2018

Hoogste punt kern EMA-gebouw Zuidas

Hoogste punt kern EMA-gebouw Zuidas

Aankomende week wordt het hoogste punt van de kern van de nieuwbouw voor het Europees Geneesmiddelenagentschap bereikt, dat heeft minister Bruins (Medische Zorg) aan de Tweede Kamer gemeld. Dit is een belangrijke mijlpaal in de verhuizing van het EMA naar Amsterdam als gevolg van de Brexit. In slechts anderhalf jaar tijd wordt een voor EMA op maat gemaakt kantoorgebouw met conferentiecentrum aan de Zuidas gerealiseerd. Voordat de nieuwbouw gereed is dient het EMA-personeel tijdelijke gehuisvest te worden...

Netherlands - Ministerie van Volksgezondheid, Welzijn en Sport

5-9-2018

Burton recalls Step On Snowboard Boots

Burton recalls Step On Snowboard Boots

The heel cleat on the boots can release from the binding unexpectedly, posing a fall hazard to the user.

Health Canada

29-8-2018

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Published on: Thu, 16 Aug 2018 00:00:00 +0200 4,15‐Diacetoxyscirpenol (DAS) is a mycotoxin primarily produced by Fusarium fungi and occurring predominantly in cereal grains. As requested by the European Commission, the EFSA Panel on Contaminants in the Food Chain (CONTAM) assessed the risk of DAS to human and animal health related to its presence in food and feed. Very limited information was available on toxicity and on toxicokinetics in experimental and farm animals. Due to the limitations in the avai...

Europe - EFSA - European Food Safety Authority Publications

14-8-2018

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix LLC, is voluntarily recalling lot: 112710 of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa capsules, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend to the consumer level. These products have been tested by the U.S. Food and Drug Administration (“FDA”) and found to be contaminated with High Microbial Loads. Additionally, this serves as a update to a previous press release posted on June 30th 2018, concerning Blissful...

FDA - U.S. Food and Drug Administration

3-8-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on new steps the agency is taking to support the development of novel nicotine replacement drug therapies to help smokers quit cigarettes

Statement from FDA Commissioner Scott Gottlieb, M.D., on new steps the agency is taking to support the development of novel nicotine replacement drug therapies to help smokers quit cigarettes

FDA releases the first of two draft guidances aimed at supporting the development of novel, inhaled nicotine replacement therapies that could be submitted for approval as new drugs.

FDA - U.S. Food and Drug Administration

1-8-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s continued, careful oversight of the REMS associated with transmucosal immediate-release fentanyl products

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s continued, careful oversight of the REMS associated with transmucosal immediate-release fentanyl products

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s continued, careful oversight of the REMS associated with transmucosal immediate-release fentanyl products

FDA - U.S. Food and Drug Administration

14-2-2019

EU/3/05/296 (Diurnal Europe B.V.)

EU/3/05/296 (Diurnal Europe B.V.)

EU/3/05/296 (Active substance: Hydrocortisone (modified release tablet)) - Transfer of orphan designation - Commission Decision (2019)1358 of Thu, 14 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000002750

Europe -DG Health and Food Safety

14-2-2019

EU/3/08/554 (IDEA Innovative Drug European Associates (Ireland) Limited)

EU/3/08/554 (IDEA Innovative Drug European Associates (Ireland) Limited)

EU/3/08/554 (Active substance: Beraprost sodium (modified release tablet)) - Transfer of orphan designation - Commission Decision (2019)1354 of Thu, 14 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003232

Europe -DG Health and Food Safety

6-2-2019

Release for supply of medicines

Release for supply of medicines

Release for supply guidance has been restructured and updated to be consistent with PE009-13

Therapeutic Goods Administration - Australia

1-2-2019

Diotop 75 mg / 20 mg modified-release capsules, hard and associated names

Diotop 75 mg / 20 mg modified-release capsules, hard and associated names

Diotop 75 mg / 20 mg modified-release capsules, hard and associated names (Active substance: diclofenac/omeprazole) - Community Referrals - Art 29 - Commission Decision (2019)845 of Fri, 01 Feb 2019 European Medicines Agency (EMA) procedure number: EMEA/H/A-29(4)/1474

Europe -DG Health and Food Safety

29-1-2019

On January 23rd, @US_FDA permitted the marketing of first test to aid in  the diagnosis of a sexually-transmitted infection known as Mycoplasma genitalium. For more information, read the press release here:  https://go.usa.gov/xEkt3  #FDA #MedicalDevice

On January 23rd, @US_FDA permitted the marketing of first test to aid in the diagnosis of a sexually-transmitted infection known as Mycoplasma genitalium. For more information, read the press release here: https://go.usa.gov/xEkt3  #FDA #MedicalDevice

On January 23rd, @US_FDA permitted the marketing of first test to aid in the diagnosis of a sexually-transmitted infection known as Mycoplasma genitalium. For more information, read the press release here: https://go.usa.gov/xEkt3  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

17-12-2018

Consultation: Remaking Therapeutic Goods Order No. 78

Consultation: Remaking Therapeutic Goods Order No. 78

A consultation on the remaking of Therapeutic Goods Order No 78 has been released. Have your say! Closing date: 8 February 2019

Therapeutic Goods Administration - Australia

14-12-2018

#ICYMI: Jeff Shuren, Director of the Center for Devices & Radiological  Health, released a statement on updated safety  communication about  rates of duodenoscope contamination from  preliminary postmarket data.  Read the statement here:  https://go.usa.g

#ICYMI: Jeff Shuren, Director of the Center for Devices & Radiological Health, released a statement on updated safety communication about rates of duodenoscope contamination from preliminary postmarket data. Read the statement here: https://go.usa.g

#ICYMI: Jeff Shuren, Director of the Center for Devices & Radiological Health, released a statement on updated safety communication about rates of duodenoscope contamination from preliminary postmarket data. Read the statement here: https://go.usa.gov/xE3kf  #MedicalDevice

FDA - U.S. Food and Drug Administration

5-12-2018

Updates to the Database of TGA laboratory testing results

Updates to the Database of TGA laboratory testing results

New release of results published

Therapeutic Goods Administration - Australia

4-12-2018


Overview of comments received on Ibuprofen 200 – 800 mg oral use, immediate release formulations product-specific bioequivalence guidance

Overview of comments received on Ibuprofen 200 – 800 mg oral use, immediate release formulations product-specific bioequivalence guidance

Overview of comments received on Ibuprofen 200 – 800 mg oral use, immediate release formulations product-specific bioequivalence guidance

Europe - EMA - European Medicines Agency

5-10-2018

Devices flag! The FDA has allowed the marketing a new type of hearing aid, a self-fitted hearing aid controlled by the user. Interested reporters should check out our press release:  https://go.usa.gov/xPkuB 

Devices flag! The FDA has allowed the marketing a new type of hearing aid, a self-fitted hearing aid controlled by the user. Interested reporters should check out our press release: https://go.usa.gov/xPkuB 

Devices flag! The FDA has allowed the marketing a new type of hearing aid, a self-fitted hearing aid controlled by the user. Interested reporters should check out our press release: https://go.usa.gov/xPkuB 

FDA - U.S. Food and Drug Administration

24-9-2018

#FDA announces the release of the Collaborative Communities Toolkit for interested stakeholder organizations to work together on healthcare challenges. Learn about the program, download the Toolkit, and submit comments:  https://go.usa.gov/xPjKX pic.twitt

#FDA announces the release of the Collaborative Communities Toolkit for interested stakeholder organizations to work together on healthcare challenges. Learn about the program, download the Toolkit, and submit comments: https://go.usa.gov/xPjKX pic.twitt

#FDA announces the release of the Collaborative Communities Toolkit for interested stakeholder organizations to work together on healthcare challenges. Learn about the program, download the Toolkit, and submit comments: https://go.usa.gov/xPjKX  pic.twitter.com/iQsKIAAQTn

FDA - U.S. Food and Drug Administration

24-9-2018

News and press releases:  Companies stepping up efforts to ensure medicine supply post Brexit

News and press releases: Companies stepping up efforts to ensure medicine supply post Brexit

Focus is now on 39 centrally authorised medicines, down from 108

Europe - EMA - European Medicines Agency

24-9-2018

News and press releases:  EMA to launch new corporate website on 27 September 2018

News and press releases: EMA to launch new corporate website on 27 September 2018

Fresh design and improved features to provide better user experience

Europe - EMA - European Medicines Agency

30-8-2018

Consultation: Referral of proposed amendment to the current Poisons Standard to the meeting of the ACMS, March 2019

Consultation: Referral of proposed amendment to the current Poisons Standard to the meeting of the ACMS, March 2019

Advisory Committee on Medicines Scheduling to consider upscheduling of modified release paracetamol to 'Pharmacist Only'. Closing date 31 October 2018

Therapeutic Goods Administration - Australia

30-8-2018

Modified release paracetamol

Modified release paracetamol

Advisory Committee on Medicines Scheduling to consider upscheduling of modified release paracetamol to 'Pharmacist Only'

Therapeutic Goods Administration - Australia

15-8-2018

Scientific guideline:  Draft guideline on specifications: test procedures and acceptance criteria for herbal  substances, herbal  preparations and herbal medicinal products/traditional herbal medicinal products - Revision 3 , draft: consultation open

Scientific guideline: Draft guideline on specifications: test procedures and acceptance criteria for herbal substances, herbal preparations and herbal medicinal products/traditional herbal medicinal products - Revision 3 , draft: consultation open

This document addresses specifications, i.e. those tests, procedures, and acceptance criteria used to assure the quality of the herbal substances/preparations and herbal medicinal products at release and during the shelf-life.

Europe - EMA - European Medicines Agency