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Rede Global de Consultoria em Assuntos Regulatórios

Conecte-se com nossa rede confiável de consultorias em assuntos regulatórios especializadas em registro e conformidade de dispositivos médicos nos principais mercados globais.

Mostrando 8 de 8 consultorias

Qualtech Consulting Corporation

Taiwan, China, Japan, Singapore, Hong Kong, Malaysia, Philippines, Vietnam, Australia, Germany, Korea, Thailand, USA

Registro

A specialized medical device consulting firm offering a one-stop solution for complex global regulatory challenges. We offer real-time regulatory and clinical support, local representation, and QMS services across 13 markets, ensuring efficient market entry and compliance.

Especializações

Regulatory Consulting (Product Registration)
Clinical Trials (CRO)
Local Authorized Representation
Post-Market Activity
Quality Management Systems (QMS)
Clinical Evaluation Report (CER)
Market Access Strategy

Idiomas: English, Japanese, Chinese (Mandarin & Cantonese), Korean, Thai, Vietnamese, Bahasa Indonesia, Bahasa Malaysia, German

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MedEnvoy Global

The Hague, Netherlands, London, United Kingdom, United States, Switzerland, Australia

Registro

A global regulatory compliance partner specializing in in-country representation (EC Rep, UKRP, CH Rep, US Agent) and independent importer services for medical device and IVD manufacturers. We help companies navigate complex regulations in Europe, the UK, Switzerland, and the US while maintaining supply chain flexibility.

Especializações

EU Authorized Representative (EC REP)
UK Responsible Person (UKRP)
Swiss Authorized Representative (CH REP)
US Agent
Independent Regulatory Importer (EU, UK, CH)
Regulatory Consulting
EUDAMED Registration

Idiomas: English, Dutch, German, French

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KoBridge Co Ltd

Seoul, Korea, Lausanne, Switzerland

Registro

We offer fast, effective, and flexible solutions for medical device manufacturers needing to navigate the increasing complexity of global regulations. Their core competencies cover CE Marking, FDA 510(k)/PMA, MDSAP, and especially Korea MFDS registration and KGMP compliance. They handle active, non-active, combination, and animal-origin devices, providing services from strategic planning and dossier preparation to quality system implementation (ISO 13485) and audits.

Especializações

Korea MFDS Registration
KGMP Certification and Audit
EU CE Marking (MDR/IVDR)
US FDA Regulatory Submission (510k/PMA)
MDSAP Compliance
ISO 13485 Quality System Implementation
Biological Evaluation (ISO 10993)
Clinical Evaluation Reports (CER/MEDDEV 2.7.1)

Idiomas: English, Korean, French

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Regulatory Compliance Associates Inc. (RCA)

Pleasant Prairie, WI, Tampa, FL

Registro

Regulatory Compliance Associates (RCA) is a leading global provider of regulatory and compliance expert consulting services for life science companies. The company offers expertise in regulatory affairs, assessments and audits, agency response, preparation and remediation, and new product development support for medical devices, pharmaceuticals, and compounding pharmacies.

Especializações

Medical Device Consulting
Pharmaceutical Consulting
Compounding Consulting
Regulatory Affairs
Quality Assurance
Audits and Assessments
New Product Development

Idiomas: English

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Kalms Consulting GmbH

Berlin

Registro

Provides expert guidance for healthcare companies in market access, health economics, reimbursement, and business development across Europe, with a focus on Germany.

Especializações

Market Access
Health Economics
Reimbursement
Regulatory Compliance
Business Development

Idiomas: English, German

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meditec Consulting GmbH

Boll, Switzerland

Registro

We provide consulting services to the medical device, pharmaceutical and healthcare industry. Our services include Regulatory Affairs, Quality Management, Risk Management, Trainings and Seminars.

Especializações

RA strategy
medical device and IVD regulations
preparation and submission of technical documentation for EU, USA, Canada and other markets
Quality system compliance in accordance with ISO 13485, CMDCAS and FDA QSR
FDA inspections
Notified body audits
Device Vigilance reporting
Risk- and usability management
Packaging Validation
Submission management for pharmaceuticals
EU/CH Pharmacovigilance
Regulatory Intelligence
eCTD Dossier Publishing
Variations in CH
Project Management
strategy and carrying out of documentation
technical files in development projects
training
change management and CAPA

Idiomas: English, German, French

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Regulatory Insight, Inc.

Nashville, USA

Registro

We are a consultancy specializing in FDA medical device compliance, submissions, training, and export/import services.

Especializações

FDA 510(k) Premarket Notification
FDA PMA Premarket Approval Application
FDA De Novo Reclassification Request
FDA and ISO 13485 Compliant Quality Systems
Medical Device Single Audit Program (MDSAP) Preparation
FDA 483 Warning Letter Response and Remediation
FDA Establishment Registration and Device Listing
U.S. Agent Representation for Medical Devices
Unique Device Identification (UDI) and Global Unique Device Identification Database (GUDID)
Health Canada Medical Device License (MDL) and Medical Device Establishment License (MDEL)
European Medical Device Regulation (MDR) CE mark
Australian TGA Registration for Medical Devices
Employee Regulatory and Quality Systems Training for Medical Devices
Assistance with Medical Device Import and Export Issues

Idiomas: English

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Emergo by UL

USA, Canada, Brazil, Australia, China, Hong Kong, Taiwan, India

Registro

A dedicated partner for medical device and IVD manufacturers, we offers deep local regulatory expertise through its offices in over 20 global locations. Services include product registration, human factors research, clinical strategy, and local in-country representation to ensure rapid, compliant market access worldwide.

Especializações

Idiomas: English, Chinese (Mandarin & Cantonese), Japanese, Korean, Spanish, Portuguese, German, French

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