News

Pure Global Partners with MEDIcept to Enhance Medical Device and IVD Market Entry

In a significant move to advance the medical device and in vitro diagnostics (IVD) industries, Pure Global and MEDIcept have announced a strategic collaboration designed to streamline global market access and regulatory pathways.

Published on:
May 8, 2024

This article was originally published in TechNews 180.

In a significant move to advance the medical device and in vitro diagnostics (IVD) industries, Pure Global and MEDIcept have announced a strategic collaboration designed to streamline global market access and regulatory pathways. This partnership leverages Pure Global's global market access services and MEDIcept’s expertise in US and EU regulatory, quality, and clinical services, aiming to transform challenges into opportunities across international borders.

By integrating Pure Global’s global representation and advanced AIGC regulatory tools with MEDIcept's robust US and EU market expertise, the collaboration seeks to simplify the complexities of regulatory compliance and market entry. This synergy enhances their service offerings, allowing them to provide comprehensive regulatory affairs, quality assurance, clinical support, and market representation in key regions including the US, Latin America, Europe, the Middle East, and Asia Pacific.

The collaboration is set to bring significant benefits to the industry by combining the strengths of both companies to better navigate regulatory landscapes and facilitate smoother market access. Key objectives of the partnership include expanding service reach, enhancing research capabilities through advanced tools, and designing global clinical studies to support market and post-market activities.

The companies anticipate that their joint efforts will not only drive growth and innovation within the medical device and IVD fields but also deliver greater value and efficiency to their clients worldwide. The initial stages of the alliance will focus on a joint marketing initiative to promote their expanded service portfolio.

Zhu (Phyllis) Meng, CEO of Pure Global, commented on the partnership, stating, "Pure Global's strategic alliance with MEDIcept will help accelerate MedTech innovation and streamline compliance. By combining their hundreds of successful submissions since 1996 with our AI-powered & data driven regulatory solutions, we empower clients worldwide to bring life-changing MedTech to market faster, with reduced costs and higher regulatory success.”

David Rothkopf, President of MEDIcept, added, "With this strategic alliance we are strengthening our worldwide presence and can serve the needs of our customers anywhere. With teams of seasoned consultants both MEDIcept and Pure Global offer deep expertise across a wide range of compliance needs. Together, this relationship will efficiently help international companies with FDA and US quality, regulatory, clinical, and reimbursement concerns and rapidly provide tailored, trusted solutions to meet their unique challenges."

As they move forward, both Pure Global and MEDIcept are enthusiastic about the potential of their partnership to revolutionize market access for medical technologies globally.

Subscribe to newsletter
Subscribe to receive the latest blog posts to your inbox every week.
By subscribing, you agree to our Terms and Conditions.
Thank you for subscribing!
Oops! Something went wrong while submitting the form.
Read more

Latest News

Browse our news hub featuring company announcements, regulatory updates, and industry insights to keep you informed and ahead of the curve.

Regulatory Update
January 29, 2025

Wrapping up January 2025, medical device regulatory developments include new forms for NBs in Europe, new PMS guidance in the UK, an expedited approval partnership between China and Malaysia, and warnings of supply chain disruptions for pediatric patients in the US.

Regulatory Update
January 23, 2025

Medical device regulatory developments from the US and Thailand include: final FDA guidance on modular review for premarket approval applications and humanitarian device exemptions, and new expedited regulatory routes for low-risk devices and chronic disease prevention devices in Thailand.

Regulatory Update
January 16, 2025

This week, we are reporting on medical device regulatory updates from Canada, Europe, Brazil, and China. China's NMPA released registration review timelines, clarification on MDR and IVDR vigilance terms is now available, and Health Canada updated validation rules for non-eCTD transactions.

To kick off 2025, we bring you a round up of medical device regulatory updates from across Europe and the US, including a new position paper from TEAM-NB on MDR certification processes and numerous guidance updates from the US FDA.

Contact us
Request information

Let's Talk,
Anywhere You Are.

Whether looking for more information or ready to partner with us, we're here to guide you through every step of the regulatory process.

Our closest representative will get back to you within 24 hours.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Latest Blog Content

Explore our collection of articles, success stories, and regulatory updates, designed to help you take your product global.

Blog Article

The official IVDR transition period is here. IVDR expert Dr. Oliver Eikenberg discusses how IVD manufacturers should take action, starting with how to implement IVDR QMS requirements for the May 2025 deadline.

Kuala Lumpur Malaysia Skyline
Blog Article
Pure Global Team attends IMDEC 2024 in Malaysia

Pure Global participated in IMDEC 2024 in Kuala Lumpur to discuss the latest advancements in medical technology, regulatory efficiency, and the role of AI in transforming the industry. Highlights included updates from the Malaysian Medical Device Authority (MDA) that showcased their commitment to driving regional leadership in medical device regulation and innovation.

Pure Global 2024 Year in Review
Blog Article
Pure Global 2024 Year in Review

As 2024 comes to a close, Pure Global proudly reflects on a transformative year marked by substantial growth, cutting-edge innovation, and impactful collaborations.

Risk increases compliance chalenges under IVDR
Blog Article
What are the challenges under IVDR?

IVD manufacturers cite the new classification system, detailed definitions for intended purposes, and the need for verification of clinical evidence as key challenges under the IVDR.