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Don’t miss this opportunity to network and learn at one of the premier global congresses in wound care

At the ESSKA Congress, discover an inspiring session on the future of regenerative medicine with Dr Branko Barac, MD, PhD.

Director of the Institute of Rheumatology, Belgrade, faculty member at the University of Belgrade Faculty of Medicine, President of the Republic Regulatory Committee for Rheumatology and Regenerative Medicine, and Certified EULAR MSK Ultrasound Teacher, Dr Barac will share his expert perspective on the evolution of musculoskeletal therapies.

Through his presentation, “The Next Step in Musculoskeletal Longevity: Integrating HA, PRP, and Regenerative Matrices”, he will discuss how the combination of hyaluronic acid, PRP, and regenerative matrices is opening new possibilities for enhancing mobility, supporting joint health, and promoting musculoskeletal longevity.

A session not to be missed for healthcare professionals interested in therapeutic innovation and the future of regenerative medicine.

The Next Step in Musculoskeletal Longevity: Integrating HA, PRP, and Regenerative Matrices

Thursday 21. May
Time: 12:50 -13:50
Room: Hall D3-4
Dr Branko Barac, MD, PhD

Dr Branko Barac, MD, PhD

Belgrade, Serbia

Director, Institute of Rheumatology, Belgrade | University of Belgrade, Faculty of Medicine  

Abstract

Musculoskeletal longevity reframes degenerative joint disease management toward preserving function and sustaining activity over time. Injection-based strategies have progressively evolved from hyaluronic acid (HA) viscosupplementation to autologous platelet-rich plasma (PRP), and further to PRP+HA combination approaches—aiming to integrate mechanical support with autologous biological signalling. 

This lecture proposes a structured continuum—HA → PRP → PRP+HA → regenerative matrices—to help clinicians contextualise current approaches and the emerging “next step” in longevity-oriented care. As an evidence anchor, the session reviews a prospective randomised controlled clinical comparison in knee osteoarthritis evaluating a PRP+HA cellular matrix approach versus HA-only regimens, using validated pain and functional measures across follow-up timepoints.  

A core challenge in orthobiologics remains the heterogeneity of PRP formulations and protocols, which limits comparability across trials and complicates translation to clinical practice. The lecture therefore highlights why standardisation and clear reporting are essential for reproducibility and credible adoption.   

Finally, the session briefly illustrates how translation can extend beyond clinic-level decisions into health-system evaluation, using Serbia’s osteoarthritis programme pathway described as progressing through national review and reimbursement consideration.  

The session concludes with practical takeaways on interpretation of evidence, the role of standardised preparation, and how regenerative matrices may shape future MSK longevity strategies. 

Learning Objectives

After this lecture, participants will be able to: 

Position HA, PRP, and PRP+HA as an evolving 

Explain why standardisation is central when interpreting orthobiologic evidence and translating it to practice.   

Describe the “next step” concept of regenerative matrices as a strategy to support the local tissue environment beyond injectate-only approaches. (Conceptual positioning.) 

Recognise how adoption pathways can evolve from evidence to evaluation, illustrated briefly by Serbia’s OA reimbursement workstream described as in progress/awaiting decision.   

Speaker Bio
  • Director, Institute of Rheumatology, Belgrade, Serbia  
  • Assistant Research Professor, University of Belgrade, Faculty of Medicine [  
  • President, Republic Regulatory Committee for Rheumatology and Regenerative Medicine (on behalf of the Ministry of Health of the Republic of Serbia)   
  • Certified EULAR Musculoskeletal Ultrasound Teacher  
  • Clinical and scientific focus: rheumatology, musculoskeletal ultrasound, and regenerative medicine / orthobiologics  
  • Conducted / reported a prospective randomized controlled clinical study in knee osteoarthritis comparing PRP+HA (Cellular Matrix approach) versus HA regimens, with outcomes assessed using validated pain/function scores 

About Us

Since 2003, Regen Lab SA has specialized in designing and manufacturing high-quality medical devices for cell therapies and the preparation of autologous platelet-rich plasma (PRP) from the patient's own blood for bedside procedures.

Milestones

2003 - Foundation
2010 - RegenKit first approval in bone graft
2013 - A new state-of-theart laboratory in Lausanne
2014 - Cellular Matrix first approval
2015 - Launch of Cellular Matrix in Europe

Vision

Founded in 2003, Regen Lab has become a global reference thanks to its commitment to innovation, quality, and the effectiveness of its therapeutic solutions. Here’s how we have transformed the medical landscape over the past two decades.

RegenPRP™

RegenPRP™ is a medical treatment that uses platelet-rich plasma from the patient's own blood to enhance and tissue regeneration.

RegenPRP™ - HA

RegenPRP™ - HA combination is an innovative treatment combining platelet-rich plasma (PRP) and hyaluronic acid to improve tissue regeneration and healing.

RegenPRP™ - ATS

RegenPRP™ combined with ATS (Autologous Thrombin Serum) is an advanced approach to tissue regeneration that uses autologous thrombin-enriched platelet-rich plasma (PRP) to maximise healing effects.

RegenExtracell®

RegenExtracell is an innovative tissue regeneration treatment using an extracellular matrix enriched with platelet-rich plasma (PRP).

RegenWound

RegenWound is a fully autologous solution prepared from the patient’s own blood, with the objective of providing a standardised and reproducible approach for clinical use.

Regulatory

Manufacturers of medical devices based outside the EU must designate an Authorized Representative (EU-REP) established within the EU in order to meet the CE requirements for placing medical devices on the EU market.

Quality Management

Regen Lab Quality System Management ensures the consistency of our products quality in total GMP compliance.

Our production facility rooms atmosphere is monitored to satisfy non-pyrogenic medical devices manufacturing.

Patents

As a leader in the PRP&HA regenerative field and as an innovation-driven company, Regen Lab SA has devoted important resources since 2004 to put on the market pioneering and diversified products constituting a complete set of tools/technologies for the medical community.