QR Group Explains Logistics Operations: What Medical Device Companies Need to Know
Logistics Operations: integrating compliance and efficiency in the healthcare chain Operating medical device logistics in Brazil requires absolute control of regulatory processes, inventory management, and transportation under specific conditions. QR Group’s logistics operations were developed to combine regulatory expertise with operational efficiency, offering a comprehensive service that includes planning, execution and real-time monitoring of the […]
Bonded Warehouse: Safe Storage for Healthcare Products
Bonded Warehouse: Compliance and Efficiency for Medical Devices Storing imported medical devices requires technical structure, strict management, and regulatory compliance. QR Group’s bonded warehouse service offers complete support from receipt to release for commercialization, ensuring that products are under strict control, either at the appropriate temperature or in safe areas, as required by ANVISA and […]
QR Group Explains Distribution Operations Management: What Medical Device Distributors Need to Know
Distribution Operations Management: control and efficiency in the logistics chain Managing the inventory and distribution of medical devices in Brazil requires complete visibility into inventory levels, accurate tracking, and efficient execution. QR Group offers a specialized service in the management of distribution operations, integrating technology, compliance and logistics control to ensure that your products arrive […]
QR Group performs internal audits and GMP inspections for healthcare supply chain suppliers
Find out how QR Group’s internal audits and inspections ensure compliance with RDC 665/2022 and agility in product registration Focusing on internal audits, QR Group offers Good Manufacturing Practices (GMP) inspections at suppliers, preparing manufacturers to meet ANVISA requirements and ensure compliance in records. In this text, we explain the process and benefits for medical […]
QR Group Explains ANVISA’s Good Manufacturing Practices Inspection for Medical Devices
Understand how GMP inspection impacts the registration of medical devices and how QR Group facilitates the compliance process. ANVISA requires that a Good Manufacturing Practices (GMP) Inspection be carried out at the facilities of manufacturers of risk class III and IV medical devices, whether national or international, as part of the process for product registration. […]
Anvisa Gets a Grade 10 Performance in Good Regulatory Practices: Understand the Impact and How QR Group Can Help in the Process
CGU audit recognizes Anvisa’s excellence in good regulatory practices; learn how this reflects on healthcare product regulation and how QR Group supports manufacturers. The Office of the Comptroller General of the Union (CGU) recently evaluated Anvisa, along with other regulatory agencies, regarding the adoption of good regulatory practices. Anvisa stood out for meeting all the […]
Why is Good Manufacturing Practices Training Essential in Brazil?
QR Group Explains How Training Can Be a Competitive Advantage in the Healthcare Market In Brazil, where the healthcare sector is constantly evolving, companies that invest in good manufacturing practices stand out for the quality and safety of their products. QR Group, a specialist in regulatory consulting and product registration with ANVISA, reinforces the importance […]
Spending on Medication Represents 33.7% of Brazilian Families Health Expenditure in 2021, According to IBGE
Understand how the Growth in Spending on Medication Impacts the Economy and QR Group’s Role in Access to Health Products In 2021, Brazilians spent R$168.3 billion on purchasing medications, representing 33.7% of household spending on healthcare, according to data from IBGE. This increase reflects both the impact of the pandemic and the aging of the […]
