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Experience seamless quality control with our Integrated Quality Management System. Elevate efficiency and productivity effortlessly.

Experience seamless quality control with our Integrated Quality Management System. Elevate efficiency and productivity effortlessly. The QMS requirements of the Canadian Medical Devices Regulations are included in the MDSAP. A document outlining the current good manufacturing practices requirements is the FDA 21 CFR Part 820, often known as the Quality System Regulation. A MAVEN integrated quality management system complies not only with ISO 13485, but additional medical device regulatory requirements in many other markets.

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To achieve and sustain excellence, a company needs a good quality control system. We provide Internal Quality Audit to helps organizations.

To achieve and sustain excellence, a company needs a good quality control system. We provide Internal Quality Audit to helps organizations. Internal Quality audits are typically performed at predefined time intervals as per the audit plan and ensure that the institution has clearly defined internal system monitoring procedures linked to effective action. The audits are unbiased and require cross-functionality of departments.

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Best Turnkey Project Consultancy for Medical and IVD Devices in Bangladesh

Maven Profcon Services LLP is a medical device consulting regulatory company provides regulatory guidance to medical device manufacturers in

Maven Profcon Services LLP is a medical device consulting regulatory company provides regulatory guidance to medical device manufacturers in Ecuador. We help our clients by providing turnkey project services such as quality system accomplishment, training, licensing, certification, and regulatory approval.

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Best regulatory consultant for US FDA 510K Approval in USA

Maven provide the best solution to get US FDA 510K Approval for medical equipment in Vietnam, Thailand, Malaysia and Hong Kong.

Take a premium advantage of MAVEN's Premium Organizational Management Services. These services are only for clients who are completely invested in making their plant highly compliant and are ready to consider regulatory compliance an important parameter for their organizational success and make necessary resources available to achieve the same. Maven provide the best solution to get US FDA 510K Approval for medical equipment.

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Deciphering MDCG Rules: Annex XVI Insights Revealed!

Crack the Code: Annex XVI MDCG Rules Demystified! Your key to compliance insights. Dive into the intricacies.

The newly proposed MDCG guidelines are a valuable resource for manufacturers (of products without an intended medical purpose), notified bodies, and stakeholders navigating the intricate landscape of medical device regulatory standards. A comprehensive review of these guidelines is crucial to maintain the safety and efficacy of medical devices in the market. In conclusion, when embracing these guidelines, it is crucial to understand the guiding principles and consider the similarities with medical devices.

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Classification of Medical Devices as per CDSCO in India

Detailed classification of Medical Devices and In-vitro Diagnostic Medical Devices in India. Get depth knowledge of notified and non-notifie

Medical devices in Australia are classified by CDSCO, Central Licensing Authority. Medical device other than in-vitro diagnostic medical devices are classified on basis of: Risk, Intended purpose, Duration of contact, Invasiveness- non-invasive, invasive with respect of body orifice, surgically invasive.

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Best Annual Maintenance Contract (AMC) Service Provider in India, AMC Services for Medical and IVD Devices globally

We provide best AMC service where we take complete charge of ensuring regulatory compliances of all certifications held by the manufacturer

We provide best AMC service where we take complete charge of ensuring regulatory compliance of all certifications held by the manufacturer. We acknowledge the limitations faced by such organizations and have specially curated our Annual Maintenance Contract Services, where we take complete charge of ensuring regulatory compliances of all certifications held by the manufacturer. These services include maintenance and update of quality management system, planning and performing Internal Quality Audits (IQA) and Management review meetings (MRM), Mock audits, Support during audits, closure of non-conformities and observations for both, internal and external audits. We also ensure that their technical documentation is kept up-to-date and in compliance to the regulation.

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Blog - All About MDSAP

Read our blog to get details about what is MDSAP, Participating Regulators, MDSAP Certification Audit, benefits and its transition timeline.

The Medical Device Single Audit Program (MDSAP) is a harmonised approach to auditing and monitoring the quality management systems of medical device manufacturers on an international scale. The purpose of MDSAP is to establish, conduct and command a single audit program. This allows a single audit of a medical device manufacturer’s QMS which satisfies the requirements of multiple regulatory jurisdictions.

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Navigating MDSAP in Australia: A Comprehensive Guide

Introduction

In the ever-evolving landscape of medical device regulation, manufacturers face various challenges in ensuring their products comply with the strictest standards. One such challenge is the Medical Device Single Audit Program (MDSAP), a globally recognized initiative aimed at harmonizing regulatory practices among participating countries. For medical device manufacturers seeking to market their products in Australia, MDSAP is a crucial aspect of the regulatory framework to understand and comply with. In this blog, we will delve into MDSAP in Australia, exploring what it is, its significance, and the steps to ensure compliance.

What is MDSAP?

MDSAP, the Medical Device Single Audit Program, is an international program established to promote harmonized medical device regulatory processes across multiple countries. The program allows medical device manufacturers to undergo a single audit, which satisfies the requirements of participating countries, eliminating the need for multiple audits in each country. Australia is one of the participating nations in this program.

The Significance of MDSAP in Australia

Australia's Therapeutic Goods Administration (TGA) is responsible for regulating medical devices in the country. MDSAP plays a significant role in the TGA's regulatory framework. Here are a few key reasons why MDSAP is crucial for medical device manufacturers in Australia:

1. Streamlined Auditing: MDSAP allows manufacturers to undergo a single audit process that satisfies multiple regulatory authorities, including the TGA. This streamlines the auditing process and reduces the regulatory burden for manufacturers.

2. Global Market Access: Compliance with MDSAP standards enhances the market access of medical devices, as many countries recognize the program. This opens doors to international markets for Australian manufacturers.

3. Regulatory Alignment: MDSAP aligns regulatory practices and expectations among participating countries, ensuring that medical devices meet consistent standards for quality and safety.

Steps to Ensure MDSAP Compliance in Australia

Complying with MDSAP requirements is a critical step for medical device manufacturers looking to enter the Australian market. Here are the steps to ensure MDSAP compliance:

1. Familiarize Yourself with MDSAP Requirements: The first step is to understand the MDSAP requirements and how they align with Australia's regulatory framework. The TGA's official website and MDSAP documentation are valuable resources for this.

2. Select an Authorized Auditing Organization: To undergo a MDSAP audit, you must choose an authorized auditing organization that is recognized by the TGA. Ensure the auditing organization has experience in medical device regulations and international standards.

3. Prepare for the Audit: Work closely with the selected auditing organization to prepare for the audit. This includes conducting internal audits, gathering necessary documentation, and ensuring that your quality management system complies with MDSAP standards.

4. Undergo the MDSAP Audit: The audit process involves a comprehensive evaluation of your quality management system, documentation, and procedures. The auditing organization will assess your compliance with MDSAP requirements.

5. Address Findings and Recommendations: If any non-conformities or recommendations arise during the audit, address them promptly. Corrective actions are essential to maintain compliance.

6. Submit the Audit Report to the TGA: After a successful MDSAP audit, submit the audit report and any necessary documentation to the TGA for review and certification.

7. Maintain Ongoing Compliance: MDSAP compliance is an ongoing process. Stay up-to-date with regulatory changes and ensure your quality management system continues to meet the required standards.

Conclusion

MDSAP certification is a critical component for medical device manufacturers seeking to navigate the Australian market successfully. By understanding the significance of MDSAP certification and following the outlined steps, you can streamline your entry into Australia, reduce regulatory burdens, and expand your market reach globally. Remember that compliance with MDSAP requirements is an ongoing process, requiring vigilance and adaptability to stay aligned with evolving regulatory standards in Australia and beyond. Obtaining MDSAP certification is a significant achievement that can significantly enhance your competitiveness in the global medical device industry.

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Best Consultancy to deal with different regualtories for MDSAP in USA

Our Consultancy will help you in getting MDSAP certification by dealing with different regulatory in the country like USA, India and UK thro

MDSAP is a technique through which medical device makers may be inspected once for conformity with the different medical device markets standards and regulatory requirements. Multiple individual audits or inspections by participating regulatory bodies or their representatives are replaced by a single audit. As a result, the Medical Device Single Audit Program minimizes the overall number of audits or inspections and optimises the time and resources spent on audit operations for many medical device manufacturers.

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Medical Device Technical File (MDR) as per the requirement of MDR 745/2017 in United States

We help you to prepare Medical Device Technical File (MDR) as per the regulatory requirement of EU MDR 745/2017 and submit to notified body

In Australia, medical devices are regulated by the Therapeutic Goods Administration (TGA). To gain approval for a medical device technical file in Australia, manufacturers are required to create a Technical File or Technical Documentation, which contains detailed information about the design, manufacturing, and performance of the device. Consulting with regulatory experts or the TGA is advisable to ensure that your Technical File meets all necessary criteria.

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Clinical Evaluation (CE) Solution Provider for Medical Devices in India, EUDAMED Registration in Belgium

We are the pioneer in providing CE Marking and Certification regulatorly solution in Europe. Get Clinical Evalution for your Medical Devices

Australia has implemented a new regulatory framework for CE mark for medical devices, moving away from the CE marking system used in Europe. The Therapeutic Goods Administration (TGA) in Australia is responsible for regulating medical devices. It's essential to note that regulations and requirements can change over time. I recommend checking the latest information on the TGA website or consulting with our regulatory expert to ensure compliance with current regulations regarding medical devices in Australia

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Prove Clinical Safety and Performance of your device with Literature Search Protocols and Report

We help you prepare literature search protocols using non-biased methodology such as PICO. Prepare Literature Search Report for the approval

Remember to adapt the Literature Search Protocol & Report to the specific requirements of your medical device, the Australian regulatory environment, and any internal organizational processes. It's also crucial to involve experts in the field to ensure the quality and validity of your systematic literature search and evaluation. Always consult relevant regulations and guidelines in Australia and seek expert advice when necessary.

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Demonstration of Equivalence for Medical Devices Manufacturer

Maven Profcon helps device makers demonstrate EU MDR 2017/745, MEDDEV 2.7.1 rev. 4 & MDCG 2020-5 compliance.

Medical device manufacturers in Australia related to the Demonstration of Equivalence is important for regulatory compliance and ensuring the safety and effectiveness of medical devices. Demonstrating equivalence is a crucial step in the regulatory process, as it helps establish that a new device is similar in safety and performance to a previously approved device. One of the key requirements for gaining approval for a medical device in Australia is demonstrating equivalence. This process involves showing that the new device is equivalent to a previously approved reference device in terms of safety, quality, and performance.

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Clinical Evaluation Plan for Medical Device Manufacturer

We help you in preparing Clinical Evaluation Plan as per the requirement of MEDDEV 2.7/1 and EU MDR for Medical Device Manufacturer

A Clinical Evaluation Plan is a critical document in the medical device regulatory process, outlining how you will gather and evaluate clinical data to demonstrate the safety and performance of your medical device. In Australia, medical devices are regulated by the Therapeutic Goods Administration. Additionally, consider consulting with regulatory experts or legal counsel experienced in medical device regulations in Australia to ensure compliance with the local regulatory framework.

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Clinical Evaluation Reports for Medical Device Manufacturer

We prepare and maintain a clinical evaluation report that complies with the requirements of MEDDEV and EU MDR.

A Clinical Evaluation Report is a critical document required for the regulatory approval of medical devices in Australia and many other countries. It provides a comprehensive analysis of the safety and performance of the medical device based on clinical data and relevant scientific literature. Manufacturers should ensure compliance with the latest regulations set by the TGA and other relevant authorities. Additionally, consulting with regulatory experts, clinicians, and medical writers is recommended to create a robust and accurate Clinical Evaluation Report.