M-Click V2 est un logiciel de gestion de cabinet médical nouvelle génération, complet, Plus simple et plus rapide que ses prédécesseurs, il a été conçu pour vous faire gagner un temps précieux
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Les solutions M-Click sont le fruit d'une longue collaboration entre des ingénieurs informaticiens et beaucoup de praticiens de différentes spécialités.
Je profite pour remercier tous ceux qui ont crû à notre volonté de développer la suite des logiciels M-Click et qui nous ont aidé dès nos premiers pas à réaliser ce rêve.
Je n'oublies pas aussi de remercier la jeune équipe des ingénieurs qui ont montré tout au long du chemin, leurs engagements et leurs volontés de réussir ce projet.
Aujourd'hui, je ne peux qu'être fière de voir le logiciel fonctionnel chez nos chers médecins, et je leurs promet la continuité d'un bon Service Après Vente (SAV) et plus d'innovations pour mieux servir tous les professionnels de santé.
Gestion du dossier patient (Fiche patient, Fiche médicale, …).
Gestion des Rendez-vous
Module consultation avec assistance à la saisie et une grande ergonomie.
Plusieurs modules de spécialités (Cardio, pédiatrie, gynécologie, …)
Gestion des comptes rendus
Module de biométrie entièrement paramétrable
The media included in M22‑A3 are derived from the CAP surveys and are well established for the recovery of clinically significant microorganisms. Exemption from routine QC by the clinical laboratory assumes that an overall quality program correlates test methods with clinical information and monitors test procedures and specimen quality.
The document is officially titled Quality Control for Commercially Prepared Microbiological Culture Media; Approved Standard—Third Edition . It serves as a regulatory and practical roadmap for laboratories and media manufacturers.
: You can still find the full 44-page PDF version for purchase on the CLSI Shop or authorized retailers like the ANSI Webstore .
Is your laboratory currently preparing for an (e.g., CAP or Joint Commission)?
Deviations indicate pH shifts or incorrect preparation. clsi m22a3 pdf
Upon receipt of every shipment, laboratory personnel must visually inspect the media for: Visible mold or bacterial colonies.
The Centers for Medicare & Medicaid Services (CMS) no longer recognizes the categories of “exempt” and “nonexempt” media for QC purposes. As of January 2016, CMS directs laboratories to develop an for applicable media used in their facilities, or to follow the CLIA quality assurance regulations as written.
Chocolate Agar (when used specifically for isolating Haemophilus or Neisseria species) Selective media for fastidious anaerobes
The CLSI M22-A3 guideline is available for purchase on the CLSI website. Laboratories and healthcare professionals can access the guideline in PDF format, which provides a convenient and easily accessible resource for susceptibility testing. The media included in M22‑A3 are derived from
This article provides a comprehensive overview of the CLSI M22-A3 standard, its core methodologies, its impact on laboratory workflows, and how modern digital adaptations—such as locating a —influence contemporary laboratory compliance. What is CLSI M22-A3?
You're looking for the CLSI M22-A3 PDF!
While M22-A3 remains an incredibly famous and widely cited document in laboratory medicine, professionals searching for this standard must be aware of its regulatory evolution. The Shift to CLSI M22-Ed4
Understanding CLSI M22-A3: The Standard for Quality Control of Microbiological Culture Media It serves as a regulatory and practical roadmap
The document, titled Quality Control for Commercially Prepared Microbiological Culture Media , is a critical standard used by microbiology laboratories to ensure the reliability of their culture media while optimizing operational efficiency. Published by the Clinical and Laboratory Standards Institute (CLSI) , this third edition established the widely used "exempt" media list based on extensive performance data. Understanding the CLSI M22-A3 Standard
is the globally recognized standard for performing quality control (QC) on commercially prepared and user-prepared microbiological culture media . Published by the Clinical and Laboratory Standards Institute (CLSI), this document ensures that the media used in clinical laboratories can reliably support the growth of pathogens while inhibiting non-pathogenic organisms.
Sealed packaging must remain intact to prevent dehydration, which alters the osmotic pressure of the medium and inhibits bacterial growth. Step-by-Step Quality Control Testing Protocol
It clarifies the specific duties of the manufacturer, the distributor, and the end-user laboratory. Where to Obtain the Document
