Warm, curious, and gently funny, this episode reminds us that even something as small as a sneeze can tell a story about what it means to be alive. 🧠 Topics covered: How sneezing actually works (and why we can’t do it in our sleep) Sunlight, pepper, and other surprising sneeze triggers Cultural myths and history of “God bless you” Why sneezing connects us more than we think 💬 “Be good to your noses, be kind to your bodies… and stay curious.”

Take a look at the key strategies to keep Salmonella at bay throughout the poultry production chain in this episode of WATT Poultry Podcast featuring Marcos Rostagno, DVM, Ph.D., U.S. technical and innovation director with Trouw Nutrition, and Mark Clements, editor-in-chief poultry, with WATT Global Media.

SÉTIMO DIA!! SETE DIAS PARA MOLDAR SUA VIDA

Episode ini mengupas persyaratan sistem manajemen mutu (QMS) yang sebenarnya dari COFEPRIS untuk pendaftaran alat kesehatan di Meksiko. Kami menjelaskan mengapa meskipun sertifikasi ISO 13485 tidak wajib secara hukum, bukti adanya QMS yang kuat adalah suatu keharusan praktis, dan membahas berbagai dokumen alternatif yang diterima yang dapat mempercepat proses masuk Anda ke pasar.- Apakah sertifikasi ISO 13485 merupakan syarat mutlak untuk pasar Meksiko? - Dokumen apa saja yang diterima COFEPRIS

Episod ini membincangkan keperluan sistem pengurusan kualiti (QMS) untuk pendaftaran peranti perubatan di Mexico dengan COFEPRIS. Kami meneroka mengapa pensijilan ISO 13485 tidak diwajibkan secara undang-undang, tetapi bukti QMS yang mantap tetap penting. Dengarkan untuk mengetahui dokumen alternatif yang diterima seperti Tanda CE, MDSAP, dan Sijil Amalan Pengilangan Baik (GMP), serta bagaimana ini boleh mempercepatkan laluan anda ke pasaran Mexico.- Adakah pensijilan ISO 13485 satu kemestian

ในตอนนี้ เราจะสำรวจข้อกำหนดด้านระบบบริหารคุณภาพ (QMS) ของ COFEPRIS สำหรับเครื่องมือแพทย์ในเม็กซิโก เราจะชี้แจงว่าใบรับรอง ISO 13485 นั้นไม่ใช่ข้อบังคับทางกฎหมาย แต่ผู้ผลิตจะต้องแสดงหลักฐานของ QMS ที่มีประสิทธิภาพผ่านเอกสารต่างๆ เช่น ใบรับรอง CE Mark, MDSAP หรือ GMP เพื่อให้สามารถเข้าสู่ตลาดที่มีศักยภาพแห่งนี้ได้- COFEPRIS คือใคร และมีบทบาทสำคัญอย่างไรต่อตลาดเครื่องมือแพทย์ในเม็กซิโก? - การขอขึ้นทะเบียนเครื่องมือแพทย์ในเม็กซิโกจำเป็นต้องมีใบรับรอง ISO 13485 หรือไม่? - มีเอกสารทางเลือกใดบ้างที่

Tập podcast này đi sâu vào các yêu cầu của COFEPRIS, cơ quan quản lý của Mexico, đối với hệ thống quản lý chất lượng của các nhà sản xuất thiết bị y tế. Chúng tôi làm rõ liệu chứng nhận ISO 13485 có phải là bắt buộc về mặt pháp lý hay không và thảo luận về các tài liệu thay thế được chấp nhận, chẳng hạn như Dấu CE, MDSAP và Chứng nhận Thực hành Sản xuất Tốt, để chứng minh sự tuân thủ và đẩy nhanh quá trình tiếp cận thị trường.- ISO 13485 có phải là yêu cầu pháp lý bắt buộc để bán thiết bị y tế tại

Bu bölümde, Meksika'nın tıbbi cihaz düzenleyici kurumu olan COFEPRIS'in kalite yönetim sistemi (QMS) beklentilerini derinlemesine inceliyoruz. ISO 13485 sertifikasının yasal bir zorunluluk olup olmadığını ve üreticilerin bunun yerine CE İşareti, MDSAP veya İyi Üretim Uygulamaları (GMP) sertifikaları gibi hangi alternatif belgeleri sunarak uyumluluk gösterebileceklerini tartışıyoruz. Bu esnek yaklaşımın, küresel üreticilerin Meksika pazarına nasıl daha verimli bir şekilde girebileceğini keşfedin.-

I det här avsnittet utforskar vi de faktiska kraven från Mexikos regulatoriska myndighet, COFEPRIS, gällande kvalitetsledningssystem (QMS). Vi klargör myten om att ISO 13485-certifiering är ett absolut lagkrav och förklarar istället vilken dokumentation som är avgörande för en framgångsrik produktregistrering. Lär dig hur du kan använda befintliga certifikat som CE-märkning, MDSAP och GMP-intyg för att effektivisera din väg till den mexikanska marknaden.- Är ISO 13485-certifiering ett lagkrav för

यह एपिसोड मेक्सिको के COFEPRIS की गुणवत्ता प्रबंधन प्रणालियों (QMS) के लिए आवश्यकताओं की बारीकियों का पता लगाता है। हम स्पष्ट करते हैं कि क्या ISO 13485 वास्तव में अनिवार्य है और विभिन्न अंतरराष्ट्रीय स्तर पर मान्यता प्राप्त प्रमाणपत्रों, जैसे MDSAP और CE Mark, का विवरण देते हैं, जिन्हें एक मजबूत QMS के सबूत के रूप में स्वीकार किया जाता है, जिसमें 2023 के हालिया अपडेट भी शामिल हैं जो निर्माताओं के लिए पंजीकरण प्रक्रिया को सुव्यवस्थित करते हैं।- क्या मेक्सिको में चिकित्सा उपकरण बेचने के लिए ISO

In questo episodio, esploriamo i requisiti del sistema di gestione della qualità per la registrazione di dispositivi medici in Messico. Chiariremo perché l'ISO 13485, pur non essendo un obbligo di legge, è fondamentale e quali certificazioni alternative, come il Marchio CE e l'MDSAP, sono accettate dalla COFEPRIS per dimostrare la conformità e accelerare l'accesso al mercato.- L'ISO 13485 è un requisito legale obbligatorio per vendere dispositivi medici in Messico? - Quali documenti accetta la

Neste episódio, analisamos um equívoco comum sobre os requisitos regulatórios para dispositivos médicos no México. Exploramos por que a certificação ISO 13485 não é estritamente obrigatória pela COFEPRIS e detalhamos as vias alternativas que os fabricantes podem usar para demonstrar um sistema de gestão da qualidade robusto, incluindo a Marcação CE, o MDSAP e os Certificados de Boas Práticas de Fabricação.- A certificação ISO 13485 é realmente obrigatória para vender dispositivos médicos no

Cet épisode explore les exigences réglementaires de la COFEPRIS au Mexique, en se concentrant sur le rôle de la certification ISO 13485. Nous clarifions pourquoi, bien que non légalement obligatoire, la preuve d'un Système de Management de la Qualité robuste est indispensable. Découvrez les différentes formes de documentation acceptées, comme le Marquage CE et le certificat MDSAP, et apprenez comment choisir la bonne stratégie pour assurer une entrée rapide et réussie sur le marché mexicain des

ชมวิดีโอ EP นี้ใน YouTube เพื่อประสบการณ์การรับชมที่ดีที่สุด https://youtu.be/V7xr-2ULuPoHuman-ศาสตร์ อีพีนี้ ชวนตั้งคำถามว่า ถ้าเรามองว่ามนุษย์ทุกคนล้วนเป็นเผ่าพันธุ์เดียวกัน แล้วอะไรคือปัจจัยที่ทำให้เราสามารถทำร้าย จนถึงขั้นหมายเอาชีวิตกันได้ลงคอ? อะไรคือต้นตอแห่งการใช้ความรุนแรง การก่ออาชญากรรม ไปจนถึงสงครามและการสังหารหมู่ หาคำตอบผ่านแง่มุมประวัติศาสตร์และชีววิทยาได้ในเอพิโสดนี้ ดำเนินรายการโดย หมอเอ้ว-ชัชพล เกียรติขจรธาดา และ ปลายฝน-ภัทรสุดา บุญญศรี

Full Episode: Innovating Tomorrow’s Medicine ft. Rick Fultz, CEO of Acurion, Inc. whose mission is to bring the power of precision medicine to more cancer patients, faster.In this exclusive preview, Rick shares a glimpse into how Acurion is transforming the field of precision oncology using next-generation science and strategic biotech leadership.➡️ Full episode launches on 30 October 🔔 Subscribe and hit the bell so you don’t miss it!🎙️ About the Show:Innovating Tomorrow’s Medicine features bold

Treponema pallidum, the causative agent of syphilis, has been around for what seems like forever, causing major outbreaks throughout the millennia and continuing to spread at high rates, globally, into today. When it comes to diagnostic testing, some tests like RPR and VDRL have stood the test of time, having been implemented in the late 1930s and 1940s, and are now used in combination with contemporary methods like EIAs and chemiluminescent assays as the reference standard method to diagnosis

In today’s Pharmaceutical Executive Daily, we cover Eli Lilly’s partnership with NVIDIA to develop an AI supercomputer for drug discovery, a surge in biotech funding rounds and public offerings, and the FDA approval of Merck’s Winrevair for pulmonary arterial hypertension.

In this podcast episode, Jokūbas Leikauskas, Editor, BioInsights, speaks to Trevor Hallam, who served as Chief Scientific Officer of Sail Biomedicines until July 2025. The interview, recorded in June 2025, explores advances in RNA therapeutics, particularly circular RNA (circRNA or eRNA) technologies, and how they may help overcome current limitations in delivery, durability, and specificity for applications such as CAR-T cell therapies and autoimmune disease treatment.

Sit down with Kate Shaw, Founder and CEO of Innovative Trials, to explore how humanized, bespoke approaches are reshaping patient recruitment and retention in clinical research. Kate breaks down the difference between one-to-one, in-country support and automated recruitment systems, showing how local expertise and cultural understanding can dramatically improve trial outcomes. You’ll also hear how the Patient Support Center and dedicated patient navigators guide participants step by step, ens...

Darshan Kulkarni highlights that to stay compliant with the FDA, companies don’t need an exhaustive set of SOPs—just the essential ones. Inspectors primarily focus on SOPs covering informed consent, adverse event reporting, drug/device accountability, source documentation, PI oversight, protocol deviations, and record retention. He emphasizes keeping SOPs concise, practical, and enforceable, training staff consistently, and expanding them only as operational needs grow. Support the show