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""Wallach's Interpretation of Diagnostic Tests, 10th Edition serves as a practical guide to the use of laboratory tests which aids physicians in using tests more effectively and efficiently by offering test outcomes, possible meanings, differential diagnosis, and summaries of tests available. The book is organized into 2 sections. The first section is devoted to disease states. Where appropriate, a patient's chief complaint and/​or physical findings are initially presented with subsequent discussions focused on discrete disease states as they relate to a patient's chief complaint. The second section is devoted to an alphabetical listing of laboratory tests while stressing the integration of the clinical laboratory in the clinical decision making process. Test sensitivity, specific and possible and negative probabilities are included whenever appropriate. Microbiology tests are listed in a separate chapter"--Provided by publisher."

"Laboratory Medicine is an essential text for medical students and residents studying clinical pathology, medical technology students, and for practitioners working in a clinical setting. By selecting the appropriate tests and interpreting the results correctly, physicians using this book should be able to optimize patient outcomes and reduce the cost of achieving a diagnosis.This full-color guide features an easy-to-follow, consistent presentation for each disease discussed. Chapters begin with a brief description of the disorder followed by a discussion that includes tables detailing the laboratory evaluation of specific disorders, and coverage of diagnosis, baseline tests to exclude diagnostic possibilities, and clinical indications thatwarrant further screening and special testing."

"Industri farmasi harus memiliki pengawasan mutu dalam proses pembuatan obat. Produk biologi dalam bentuk parenteral dilindungi dengan kemasan primer untuk melindungi terhadap faktor lingkungan, termasuk potensi kontaminasi mikroba selama masa simpan. Penting bagi suatu industri farmasi untuk melakukan pengambilan sampel dan pengujian untuk memastikan bahwa bahan awal untuk kemasan primer yang akan digunakan memenuhi persyaratan.Pengawasan mutu rubber stopper pre-filled syringe dalam rangka uji pelolosan untuk proses produksi ini dilakukan berdasarkan metode analisis yang telah ditetapkan oleh PT Kalbio Global Medika yakni termasuk uji identifikasi FTIR, uji kadar abu, uji dimensi fisik, uji absorbansi, uji tampilan larutan, uji asiditas atau alkalinitas, uji kandungan amonium, uji extractable zinc, uji batas logam berat, dan uji residu evaporasi.Kedua sampel rubber stopperPFS yang diuji telah memenuhi persyaratan yang ditetapkan PT Kalbio Global Medika. Kedua sampel rubber stopper PFS dapat diteruskan ke Laboratorium Mikrobiologi untuk dilakukan uji endotoksin.Perlu dilakukan pengujian pengganti untuk metode analisis volatile sulfide yang tidak dapat dijalankan karena keterbatasan teknis.

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The pharmaceutical industry must have quality control in the drug manufacturing process. Biological products in parenteral form are protected with primary packaging to protect against environmental factors, including potentialmicrobial contamination during shelf life. It is important for a pharmaceutical industry to carry out sampling andtesting to ensure that the starting materials for primary packaging that will be used meet the requirements. Quality control of rubber stopper pre-filled syringes in the context of escape tests for the production process is carried out based on analytical methods that have been determined by PT Kalbio Global Medika includes FTIR identification test, ash content test, physical dimension test, absorbance test, solution appearance test, acidity or alkalinity test, ammonium content test, extractable zinc test, heavy metal limit test, and evaporation residue test. Both rubber samples The PFS stopper tested has met the requirements set by PT Kalbio Global Medika. The two PFS rubber stopper samples can beforwarded to the Microbiology Laboratory for endotoxin testing. It is necessary to carry out replacement testing for thevolatile sulfide analysis method which cannot be carried out due to technical limitations."