FOR LICENSED HEALTHCARE PROFESSIONALS
Before you choose a biologics supplier, ask what they can actually document.
The short interview clips raise useful questions. The full conversation gives you the context behind them.
Full conversation
90 min
Get the full conversation.
Request the complete interview covering biologics terminology, sourcing, processing, documentation, testing methods and the questions clinics should ask when evaluating a supplier.
No hype. No clinical claims. Just the sourcing, process and documentation questions a clinic should be able to verify.
The Dr. Pavan conversation gives clinics a framework for evaluating sourcing, processing, documentation and testing. RRG invites the same scrutiny.
Ethically donated perinatal tissue
Never embryonic or fetal tissue.
Full chain of custody
Documented from donation through delivery.
Certificate of Analysis
Provided with every lot.
FDA-registered lab
Registration is not FDA approval of any product.
Inside the conversation
What the full conversation covers
- 01TerminologyHow common biologics terms are used, where language varies between suppliers and why precise wording matters when comparing product information.
- 02SourcingWhat sourcing information a supplier can describe, and how that information is normally recorded and shared.
- 03ProcessingHow processing steps are described at a general level, and what a supplier should be able to explain about its own process.
- 04DocumentationWhat documentation is typically available for a specific product or lot, and how to ask for it.
- 05Testing methodsHow testing methods and reports are described, and how to read what a report does and does not state.
Why RRG
Why clinics take a closer look at RRG
The difference is not that RRG asks you to trust us. It is that we expect you to ask for the details.

Ask us to show you
- Where the material came from
- How custody is documented
- What testing was performed
- What documentation comes with the lot
- Who answers technical product questions after the order
- 01
Traceable sourcing
Ethically donated perinatal tissue from healthy, screened donors, never embryonic or fetal tissue, with documented sourcing and chain of custody.
- 02
Lot-level documentation
Certificates of Analysis and traceability information are attached to the product and lot information a clinic receives.
- 03
Defined processing standards
No expanded cells, defined quarantine and testing steps, and processing details our team can explain.
- 04
A real team behind the order
Access to RRG biologics consultants who can answer sourcing, processing, product and documentation questions, without crossing into clinical direction.
Conversation guide
Questions worth bringing to any supplier
This is a conversation guide only. It is not an audit, a certification, a rating or an independent review of any supplier, including RRG. Ask these same questions of RRG, not just other suppliers.
- 01Can you clearly identify where the material is sourced?
- 02Can you trace the product from source through delivery?
- 03Can you explain how the product was processed?
- 04Do you know what documentation is available for the specific product or lot?
- 05Can someone on the supplier team answer technical product questions?
- 06Does your team know where supplier education ends and clinical judgment begins?
- 07If a question comes up after the order, do you know who to call?
Product information call
Talk through supplier questions with an RRG biologics consultant.
If you are comparing suppliers, bring your questions. We will walk through what RRG can document and where our role stops.
For licensed healthcare professionals only. General information, not medical, clinical, legal or regulatory advice or professional training. There are no FDA-approved exosome products. RRG EXO products are intended for topical cosmetic use on intact skin only; not for injection, IV, systemic or therapeutic use, or to diagnose, treat, cure or prevent disease. Subject to applicable regulations and professional scope-of-practice requirements. This content is not evidence of any RRG product’s identity, purity, safety or efficacy.
Questions
Before you request it
- Who is this for?
- Licensed healthcare professionals and clinic teams who evaluate biologics suppliers. It is not patient facing and it is not intended for the general public.
- Is this clinical advice?
- No. This is general product and research information. It is not medical, clinical, legal or regulatory advice, and it is not professional training.
- Who do I meet on the call?
- An RRG biologics consultant. They can answer product information questions about sourcing, processing and available documentation. They do not provide clinical direction.
- Is the full replay sent automatically?
- Not yet. Your request is saved when you submit the form. Delivery of the full conversation will begin once the replay is connected.
- What information do you collect?
- Your work email and basic campaign details so we can send the conversation and follow up. Please do not include patient or clinical information.
