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As global clinical trials become more competitive and data-driven, Latin America is stepping up with a new global standard in clinical trial quality. In this episode, Etienne Nichols speaks with Julio Martinez-Clark, CEO of BioAccess and a key advocate for clinical site certification in Latin America.
They discuss the launch of the GCSA certification and IAOCR accreditation now available in the Americas, exploring how these standards improve site credibility, de-risk clinical trials, and offer faster pathways for medtech market access. From regulatory advantages to site selection strategies, this episode is essential listening for sponsors, CROs, and MedTech leaders navigating global trials.
Key Timestamps00:02 – Introduction to Julio Martinez-Clark and episode overview
02:10 – What is GCSA and IAOCR certification?
06:00 – Why certification is emerging now: volume, complexity, and patient safety
09:42 – Certification structure: site vs. individual requirements
13:45 – The Colombian model: First mover in Latin America
17:55 – Global harmonization vs. local certification pitfalls
21:30 – Measuring ROI of certified vs. non-certified sites
26:15 – Future of global site certification and Latin America’s role
30:00 – Regional differences: speed vs. patient pool in trial site selection
36:15 – Final thoughts on FDA trends and LATAM’s emerging position
Quotes“It’s appalling that in an industry that deals with lives, there was no global standard to certify site or individual competency—until now.”– Julio Martinez-ClarkWhy it matters: This underscores the critical gap in clinical research infrastructure and the urgent need for standards like GCSA.Analogy: Think of GCSA like ISO 9001, but for clinical research sites. It standardizes operational quality and ensures consistent patient safety practices across global locations.
Beginner Example: If a sponsor is choosing between two hospitals, and one has a GCSA badge—it’s like choosing a restaurant with a food safety grade. It builds immediate trust.
Poll Question:
What’s your biggest challenge when selecting global clinical trial sites?
Engagement Prompt:
Have you worked with certified sites or accredited professionals in your clinical trials? Share your experiences or questions with us at [email protected].
FeedbackEnjoying the Global Medical Device Podcast? Let us know what topics you want to hear next or leave us a review on your podcast platform of choice. We love your feedback—email us at [email protected] for a personalized reply.
Sponsor MessageThis episode is brought to you by Greenlight Guru, the only MedTech Lifecycle Excellence Platform designed to accelerate product development and ensure clinical compliance. Learn more at www.greenlight.guru.
4.8
9191 ratings
As global clinical trials become more competitive and data-driven, Latin America is stepping up with a new global standard in clinical trial quality. In this episode, Etienne Nichols speaks with Julio Martinez-Clark, CEO of BioAccess and a key advocate for clinical site certification in Latin America.
They discuss the launch of the GCSA certification and IAOCR accreditation now available in the Americas, exploring how these standards improve site credibility, de-risk clinical trials, and offer faster pathways for medtech market access. From regulatory advantages to site selection strategies, this episode is essential listening for sponsors, CROs, and MedTech leaders navigating global trials.
Key Timestamps00:02 – Introduction to Julio Martinez-Clark and episode overview
02:10 – What is GCSA and IAOCR certification?
06:00 – Why certification is emerging now: volume, complexity, and patient safety
09:42 – Certification structure: site vs. individual requirements
13:45 – The Colombian model: First mover in Latin America
17:55 – Global harmonization vs. local certification pitfalls
21:30 – Measuring ROI of certified vs. non-certified sites
26:15 – Future of global site certification and Latin America’s role
30:00 – Regional differences: speed vs. patient pool in trial site selection
36:15 – Final thoughts on FDA trends and LATAM’s emerging position
Quotes“It’s appalling that in an industry that deals with lives, there was no global standard to certify site or individual competency—until now.”– Julio Martinez-ClarkWhy it matters: This underscores the critical gap in clinical research infrastructure and the urgent need for standards like GCSA.Analogy: Think of GCSA like ISO 9001, but for clinical research sites. It standardizes operational quality and ensures consistent patient safety practices across global locations.
Beginner Example: If a sponsor is choosing between two hospitals, and one has a GCSA badge—it’s like choosing a restaurant with a food safety grade. It builds immediate trust.
Poll Question:
What’s your biggest challenge when selecting global clinical trial sites?
Engagement Prompt:
Have you worked with certified sites or accredited professionals in your clinical trials? Share your experiences or questions with us at [email protected].
FeedbackEnjoying the Global Medical Device Podcast? Let us know what topics you want to hear next or leave us a review on your podcast platform of choice. We love your feedback—email us at [email protected] for a personalized reply.
Sponsor MessageThis episode is brought to you by Greenlight Guru, the only MedTech Lifecycle Excellence Platform designed to accelerate product development and ensure clinical compliance. Learn more at www.greenlight.guru.
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