Why study with us
Do You Want to Understand exosmart™?
We make evidence-based training accessible to physicians and distribution partners around the world. Our Academy provides clear product education, clinical evidence, and practical knowledge, while showing where the evidence is strong, where it is still emerging, and where it stops.

ABOUT THE ACADEMY

Training on one device, written by the company behind it
— and 
built so you can check us.


Two audiences: doctors who use exosmart™, and the partners who distribute it. Written, produced and paid for by Global Regenerative Group, the company behind exosmart™.


It is not accredited CME or CPD. No outside body has reviewed it, and the certificates are training records rather than qualifications. What follows is how the modules are built, who checks them, and where the evidence runs out.


Most device training tells you what works. This one tells you where the evidence 
stops.


The usual product training is marketing with a certificate attached. It explains what a device does. It rarely explains what the evidence actually shows, and it almost never explains where that evidence runs out.

We built this the other way round. Every claim in a module 
traces to a named source. The strength of the evidence is on the page, so you can see at a glance whether you are looking at something measured in this device, something measured in a device made the same way, or something from the wider platelet-rich plasma literature. Trials that found no benefit are taught with the same weight as the ones that did. Where there is no study, the module says there is no study.

This is not caution for its own sake. A doctor who knows 
precisely where the evidence ends can hold a treatment decision under questioning from a patient, a colleague or a regulator.


A cartridge, 870 hollow fibres, and no purification step


Normal text.exosmart™ is a CE-marked Class IIa medical device: a singleuse cartridge that concentrates a patient's own plasma at the point of care by pushing it along the inside of hollow fibres whose walls hold back anything above roughly 15 kilodaltons.


Blood is drawn and spun on site. Both parts of the plasma go into the device together, the platelet-rich and the platelet-poor — around 30 mL from a 60 mL draw — and pass through 870 fibres. Water and small molecules leave through the fibre walls. Extracellular vesicles, platelets, growth factors, other signalling molecules and the larger plasma proteins stay in. About 6 mL comes out.


There is no isolation step, no purification step and no fractionation step, and that is deliberate. A filter designed to isolate vesicles alone would use a size limit in the hundreds of kilodaltons and would let the proteins wash away. This one keeps them, so the vesicles, the growth factors and the plasma proteins arrive together, the way they travel in blood. That is why we describe the output as the complete autologous plasma secretome rather than as platelet-rich plasma or as isolated vesicles.



The concentration step takes three to five minutes; with the draw and the spin the full workflow is on the order of ten to twenty minutes. The preparation is autologous throughout, and no chemical activator is added.

Doctors and distribution partners, taught separately


The same science, two different jobs. A doctor decides which 
patient to treat and which not to. A partner has to explain the science to a doctor without overstating it, because the doctor will check. Access to the clinical training is verified.


Doctors
Verified access · certification, continuing education and open reference


Mechanism from the primary data. Evidence graded by condition, including the conditions with no controlled e
vidence at all. Patient selection, contraindications and realistic expectations. Certification modules run in sequence and are assessed; continuing education is open to watch in any order.


Distribution partners
Onboarded access · commercial certification and reference


The science first, then commercial adoption, positioning and 
unit economics. Clinical modules are open as reference, so a partner can answer a question in the room instead of promising to come back. Treatment detail stays where it belongs, in the doctors' track.

Five rules, and the one that costs us something

They govern every module in this Academy. They exist because we are not a neutral party,
and you should not 
have to take our word for anything. 


WHAT RULE FOUR LOOKS LIKE IN PRACTICE

Platelet factor 4 is one of the most abundant proteins in a platelet granule, so this device retains and concentrates it along with everything else. A study published in 2020 found that it inhibits the growth of human hair follicles. That finding sits inside our hair modules, next to the reasons the whole-fraction approach makes sense, because a doctor who hears it from us is not ambushed by it in a 
conference hall.

ABOUT THE ACADEMY

Training on one device, written by the company behind it
— and 
built so you can check us.


Two audiences: doctors who use exosmart™, and the partners who distribute it. Written, produced and paid for by Global Regenerative Group, the company behind exosmart™.


It is not accredited CME or CPD. No outside body has reviewed it, and the certificates are training records rather than qualifications. What follows is how the modules are built, who checks them, and where the evidence runs out.


Most device training tells you what works. This one tells you where the evidence 
stops.


The usual product training is marketing with a certificate attached. It explains what a device does. It rarely explains what the evidence actually shows, and it almost never explains where that evidence runs out.

We built this the other way round. Every claim in a module 
traces to a named source. The strength of the evidence is on the page, so you can see at a glance whether you are looking at something measured in this device, something measured in a device made the same way, or something from the wider platelet-rich plasma literature. Trials that found no benefit are taught with the same weight as the ones that did. Where there is no study, the module says there is no study.

This is not caution for its own sake. A doctor who knows 
precisely where the evidence ends can hold a treatment decision under questioning from a patient, a colleague or a regulator.


A cartridge, 870 hollow fibres, and no purification step


Normal text.exosmart™ is a CE-marked Class IIa medical device: a singleuse cartridge that concentrates a patient's own plasma at the point of care by pushing it along the inside of hollow fibres whose walls hold back anything above roughly 15 kilodaltons.


Blood is drawn and spun on site. Both parts of the plasma go into the device together, the platelet-rich and the platelet-poor — around 30 mL from a 60 mL draw — and pass through 870 fibres. Water and small molecules leave through the fibre walls. Extracellular vesicles, platelets, growth factors, other signalling molecules and the larger plasma proteins stay in. About 6 mL comes out.


There is no isolation step, no purification step and no fractionation step, and that is deliberate. A filter designed to isolate vesicles alone would use a size limit in the hundreds of kilodaltons and would let the proteins wash away. This one keeps them, so the vesicles, the growth factors and the plasma proteins arrive together, the way they travel in blood. That is why we describe the output as the complete autologous plasma secretome rather than as platelet-rich plasma or as isolated vesicles.



The concentration step takes three to five minutes; with the draw and the spin the full workflow is on the order of ten to twenty minutes. The preparation is autologous throughout, and no chemical activator is added.

Doctors and distribution partners, taught separately


The same science, two different jobs. A doctor decides which 
patient to treat and which not to. A partner has to explain the science to a doctor without overstating it, because the doctor will check. Access to the clinical training is verified.


Doctors
Verified access · certification, continuing education and open reference


Mechanism from the primary data. Evidence graded by condition, including the conditions with no controlled e
vidence at all. Patient selection, contraindications and realistic expectations. Certification modules run in sequence and are assessed; continuing education is open to watch in any order.


Distribution partners
Onboarded access · commercial certification and reference


The science first, then commercial adoption, positioning and 
unit economics. Clinical modules are open as reference, so a partner can answer a question in the room instead of promising to come back. Treatment detail stays where it belongs, in the doctors' track.

YOU WANT THE TRAINING
Create an account
Free. Clinical modules unlock once your professional registration is verified.
YOU WANT THE DOCUMENTS
academy@exosmart.co
Instructions for use, CE certificate, declaration of conformity, technical specification. Ungated — tell us which you need.
YOU WANT TO TALK TO SOMEONE
exosmart.co
Device enquiries, distribution, investigator-initiated studies and clinical collaboration.
Created with