produk: 2-Chlorophenothiazine
NO. CAS: 92-39-7
NO. EINECS: 202-152-5
Formula molekul: C12H8ClNS
Berat molekul: 233.72
Kesucian: 98%
watak: White or Grey powder
Permohonan: Ia digunakan sebagai perantaraan chlorpromazine hydrochloride
Pembungkusan: 25kg/dram
S: Bagaimanakah anda melayan aduan kualiti?
Kami mempunyai Prosedur untuk mengendalikan aduan pelanggan, salin seperti berikut:
4.1.1Jabatan jualan bertanggungjawab untuk pengumpulan maklumat aduan pelanggan dan pengendalian aduan pelanggan kerana kualiti bukan intrinsik produk; Maklumat aduan yang dikumpul hendaklah dihantar kepada jabatan kawalan kualiti tepat pada masanya. Jabatan pengurusan kualiti bertanggungjawab untuk mengendalikan aduan kualiti produk. Pengendali harus mempunyai pengetahuan profesional dan pengalaman kerja yang kaya dan dapat menilai secara objektif pendapat pelanggan.
4.1.2 Semua komen pelanggan hendaklah dimajukan segera kepada pengendali aduan pelanggan, dan tiada orang lain akan mengendalikannya tanpa kebenaran.
4.1.3Setelah menerima aduan pelanggan, pengendali hendaklah segera mengetahui punca aduan, menilainya, menentukan jenis dan jenis masalah, dan mengambil langkah tepat pada masanya untuk menanganinya.
4.1.4Apabila memberi respons kepada pelanggan, pendapat pemprosesan harus jelas, bahasa atau nada harus sederhana, supaya pelanggan faham dan mudah diterima sebagai prinsip.
4.2Failkan rekod aduan pelanggan
4.2.1Semua aduan pelanggan hendaklah direkodkan dalam bentuk bertulis, termasuk nama produk, nombor kelompok, tarikh aduan, kaedah aduan, sebab aduan, langkah rawatan, keputusan rawatan, dsb.
4.2.2 Mengekalkan analisis trend aduan pelanggan. Jika terdapat sebarang trend buruk, kenal pasti punca dan ambil tindakan pembetulan yang sewajarnya.
4.2.3Rekod aduan pelanggan dan maklumat lain yang berkaitan hendaklah difailkan dan disimpan.
2 chlorophenothiazine
92 39 7
chlorophenothiazine
Baca Berita Terkini Kami
Apr.16，2026
Strategic Growth and Quality Guide for api pharma business
The global pharmaceutical landscape is evolving rapidly, placing a heightened emphasis on the quality and reliability of Active Pharmaceutical Ingredients (APIs). Navigating the api pharma business requires a deep understanding of regulatory compliance, chemical synthesis innovation, and supply chain resilience. For companies aiming to scale, the ability to source high-purity intermediates and maintain stringent quality control is the cornerstone of success. In this guide, we will explore the critical components of managing a successful API enterprise, from regulatory hurdles to the integration of green chemistry, ensuring your business remains competitive in an increasingly demanding market.
Baca Lagi
Apr.09，2026
Importance and Quality Standards of api of pharmaceutical
In the complex world of drug manufacturing, the api of pharmaceutical, or Active Pharmaceutical Ingredient, serves as the biological heart of any medication. While a pill may contain various fillers, binders, and coatings, the API is the specific component responsible for producing the desired therapeutic effect in the patient. Ensuring the purity, stability, and efficacy of these ingredients is not just a technical requirement but a critical safety mandate for global healthcare. From simple pain relievers to complex oncology treatments, the quality of the API dictates the success of the final medical product.
Baca Lagi
Apr.07，2026
Comprehensive Guide to API of Drugs Global Sourcing and Quality Control
In the complex world of pharmaceutical ingredient sourcing, understanding the API of drugs – Active Pharmaceutical Ingredients – is paramount. These are the biologically active components that produce the intended effects in medications. This article will provide a detailed overview of APIs, their sourcing, quality control, and the role of trusted suppliers like KXD Chem in navigating the global market. Effective API sourcing is crucial for pharmaceutical companies aiming for cost-efficiency, quality, and regulatory compliance.
Baca Lagi