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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 5 de 5 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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Registrar Corp

Hampton, Virginia (HQ), Shenzhen, China, London, United Kingdom, Paris, France, Madrid, Spain, Hyderabad, India, Kuala Lumpur, Malaysia, Tel Aviv, Israel, Guatemala City, Guatemala, Cape Town, South Africa

Registro

A global FDA compliance firm assisting businesses in the food, medical device, drug, and cosmetic industries with registration, U.S. Agent services, labeling, and regulatory software solutions.

Especializações

FDA Registration & Renewal
U.S. Agent Services
Labeling & Ingredient Review
MoCRA Compliance (Cosmetics)
Food Safety (FSMA/PCQI)
Detention Assistance
Medical Device Listing (510k assistance)
Drug Establishment Registration
Adverse Event Management

Idiomas: English, Chinese (Mandarin & Cantonese), Spanish, French, German, Italian, Japanese, Korean, Portuguese, Russian, Hindi, Arabic, Thai, Vietnamese, Indonesian

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ARQon Pte. Ltd.

Singapore (HQ), Malaysia, Vietnam, Indonesia, Philippines, Thailand, Taiwan, Hong Kong, South Korea, Switzerland, USA, Australia, New Zealand, Rwanda, India, Sri Lanka

Registro

We are a premier regulatory consultancy firm specializing in medical devices, in-vitro diagnostics (IVD), and pharmaceuticals. Founded in 2014, the company offers a comprehensive suite of services ranging from product development strategy and clinical trials to product registration and post-market surveillance. With a team of experts possessing vast experience in regulatory authorities and industry, we bridge the gap between scientific innovation and regulatory compliance, ensuring patient safety while fostering medical advancement. The company also provides unique business matching services through its ATTOPOLIS platform and training through the International Medical Device School.

Especializações

Medical Device Product Registration
In-Vitro Diagnostics (IVD) Registration
Drug & Cosmetic Registration
Quality Management Systems (ISO 13485, GDPMDS)
Clinical Trials & Evaluation
Local Authorized Representative
License Holding
Global Market Strategy
Distributor Search (ATTOPOLIS)

Idiomas: English, Chinese (Mandarin), Malay, Vietnamese, Thai, Korean, German

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EPSI GLOBAL PTE. LTD.

Singapore (HQ), Kuala Lumpur, Malaysia, Jakarta, Indonesia, Bangkok, Thailand, Hanoi, Vietnam, Manila, Philippines, Shanghai, China

Registro

We provide end-to-end regulatory solutions covering all classes of medical devices and IVDs in major APAC markets, especially the ASEAN region (Singapore, Malaysia, Indonesia, Thailand, Vietnam, Philippines) and major Northeast Asian markets (China, Korea, Japan). Services include classification, registration, local authorized representation, quality management system (QMS) implementation/auditing (ISO 13485/local GMP), and post-market surveillance. Their local presence minimizes market entry risks and time-to-market.

Especializações

ASEAN Regulatory Registration
Singapore HSA Registration
Malaysia MDA Registration
Indonesia MoH Registration
Thailand FDA Registration
Vietnam MoH Registration
Philippines FDA Registration
China NMPA Registration
ISO 13485/Local GMP QMS Consulting
Local Authorized Representative (AR) Services

Idiomas: English, Chinese (Mandarin), Malay, Vietnamese, Thai, Indonesian

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Pacific Bridge Medical

USA, China, Japan, Singapore, Hong Kong, India (Affiliate), Indonesia (Affiliate), Korea (Affiliate), Malaysia (Affiliate), Philippines (Affiliate), Taiwan (Affiliate), Thailand (Affiliate), Vietnam (Affiliate)

Registro

A boutique consulting firm specializing in Asian medical and pharmaceutical regulatory affairs and business development. We provide comprehensive, on-the-ground support for market entry, registration, quality compliance, and local agent representation across 12 Asian markets.

Especializações

Regulatory Strategy
Product Registration
Market Access/Reimbursement/Health Economics
Quality Compliance
Local Agent Representation
Clinical Trials
Business Strategy
Distributor Search
Sourcing & Manufacturing
Acquisitions, Joint Ventures, & Licensing
Recruiting

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

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