Regdesk ทางเลือก & คู่แข่ง
RegDesk is an A.I.-powered medical regulatory company with software that enables you to register products all over the world and track medical regulations.
ทางเลือกและคู่แข่งของ regdesk.co ในแง่ของเนื้อหา การจราจร และโครงสร้าง
LICENSALE® is a global medical device registration system that lets you take full control of your regulatory affairs and gain approvals in 140 countries.
Thema-med.com is ranked number 10M in the world.
Asiaactual.com is ranked number 3317544 in the world and links to network IP address 23.253.73.184.
Freyr is a Global Regulatory Solutions and Services company, focusing on the entire Regulatory value-chain ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions to post approval maintenance, Labeling, Artwork Change Management for Pharmaceutical, Generics, Medical Device, biotechnology, Biosimilar, Consumer Healthcare, Cosmetic companies across the globe.
Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
ARQon is a medical device consultant for Regulatory, Quality RA/QA, device registration, clinical trials, ISO13485, GDPMD, MDSAP and distribution consulting.
Andaman Medical specialises in medical device regulatory and clinical affairs, product registration, quality compliance in Southeast Asia/ASEAN.
Keep Calm and start creating your MDR Transition Plan - Medical Device Regulation.
Medical Device consulting services - regulatory and quality - FDA, CE marking, ISO 13485, MDSAP, biological and clinical evaluation.
Germany based EU Authorized Representative "mdi Europa" helps small to medium sized manufacturers to enter european medical device market.
Qualtech is an international medical device consulting firm operating in Asia, North America, and EU. With a focus on Regulation, Market Access, and Clinical Trials.
Asia Medical Device & Pharmaceutical Consulting - Pacific Bridge Medical.
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
Home - Global Regulatory Partners, Inc.
EXTEDO is a leading RIM & eCTD solutions and services provider with 850 life sciences customers in 60 countries, including 35+ regulatory authorities.
Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to Lifesciences companies across the globe.
Want to Master Medical Device Regulation & learn how to put a product on the market in Europe. Easy Medical Device is a platform for tools and resources for Regulatory Affairs, Quality Management, Regualtory Compliance. Learn how to choose your notified body or how the device regulation is different in other countries
Celegence provides you with leading life sciences regulatory solutions & services for medical writing, medical device regulations, labeling, IDMP and more.
Der Regulatory Affairs Blog für alle Themen rund um die internationale Zulassung von medizintechnischen Produkten.
Qualtech.com.tw is ranked number 10M in the world and links to network IP address 124.150.132.79.
I3cglobal.com is ranked number 10M in the world.
EUDAMED services: EUDAMED UDI submission software, EUDAMED consultancy, training, and MDR, MDD, IVDD, AIMDD, SPP & IVDR EUDAMED device templates
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (EU MDR).
Ensure 100% medical compliance. Decomplix does your CE certification for medical devices and IVD in the pre- and post-market phase. Learn more here.
Regulatory Globe offers Expert Regulatory Affairs strategies and helpful implementation tools for medical devices. Stay updated with EU MDR, IVDR and more.
The leading MedTech Services provider, offering Medical Device Consulting, clinical trial, lab & reimbursement services to support the entire product lifecycle.
THIS WEBSITE IS ON SALE!! GET THE READER FLOW YOU NEED TO PROMOTE YOUR PHARMA CONSULTING BUSINESS!! 1,500 VISITORS A MONTH AND GROWING. GET IN TOUCH! inesitag@hotmail.com / maria@latampharmara.com Welcome! This platform and blog focuses on regulatory affairs for pharmaceutical products in Latin American markets. We run this website because we believe that making information readily…
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
Morulaa.com is ranked number 10M in the world and links to network IP address 162.241.252.188.
China Med Device - specialize in accelerating Western medtech companies with turn-key solutions for China FDA regulatory&CRO services and commercialization.
Greenlight Guru brings modern QMS and EDC software to 1,000+ medical device companies helping improve speed and efficiency while reducing risk.
World leading Wellkang Tech Consulting group help you in (CE Marking) CE Mark (EC Mark) approval, ce testing for Medical Devices (MDD), Personal Protective Equipment (PPE), Low Voltage Electrical Equipment (LVD), Electromagnetic Compatibility (EMC), Machinery, Toys, etc
Plateforme unifiée de gestion du contenu et de l'information pour soutenir le développement des produits des sciences de la vie : Qualité, Clinique, Réglementaire, Pharmacovigilance, Commercial
GreatFour Systems is one of the leading enterprise software company for Packaging, Labeling, Proofing, Regulatory and Project Management solutions.
Our team of Medical Device Regulatory Consultants are specialists offering tailored EU MDR Compliance services.
Freyrtechnology.com is ranked number 10M in the world.
Are you a start-up device company that needs medical device consulting services and training for an FDA 510k submission?
Our experts accelerate regulatory process and regulatory strategy submission and innovations worldwide through customized, tech-enabled regulatory solutions.
Software and Regulatory Services for eCTD Submissions │GlobalSubmit.
The world's only 100% medical device-focused, full development Contract Research Organization (CRO). Learn how to accelerate your development program today!
LORENZ Life Sciences: The eRegulatory Affairs Experts.
Das Johner Institut unterstützt Medizinprodukte-Hersteller bei der normenkonformen und effizienten Entwicklung ihrer Produkte und dem Aufbau von QM-Systemen durch Beratung, Seminare, Bücher und Videotrainings.
Mdb.gov.my is ranked number 10M in the world and links to network IP address 103.245.88.79.
The Regulatory Writing Experts
Cite Medical Solutions is the leader in EU MDR (medical device regulatory) consulting, high-quality literature search, and post market surveillance systems. Contact today!
Agatha provides intelligent document management applications for life sciences companies including clinical trial management, quality management, regulatory management and standard operating procedures
