Verified practices unlock a working library for sourcing, documentation and research
The Members Network gathers the practical layer our public guides point to: sessions with our chemists, templates, tools and technical documents. It opens to licensed practices after NPI verification and a review by our team.
27 resources across six areas, 6 open to approved members today and the rest on the way.
Registration takes about two minutes. Access opens after NPI verification and a review by our team, usually 1 to 3 business days. No payment details.
Access opens in three steps after you register
Every resource opens on the same review, so one approval unlocks the whole network. Tier perks open as your practice reaches the Volume, Enterprise or Elite tier of the Volume Partner Program.
1
Register your practice
Create a portal account with your practice details.
2
Verify your NPI
Submit the NPI of the licensed practitioner who orders.
3
Review by our team
A person reviews every application, usually within 1 to 3 business days.
How to read the cards
Each card says what unlocks it. "Open to approved members" means the resource is ready today; "Coming soon" means it is in production; "Waitlist open" means approved members can hold a place now; a tier note names the service tier that opens it.
Expert access
Members get time with the people who source and document their supply
Sessions cover sourcing, storage, documentation and research readiness. Product selection and clinical decisions stay with your practice.
Strategy sessions with Benn Bluestein-VeyraBook one-to-one time with our founding chemist on sourcing, characterization, storage, documentation and IND readiness. Every session ends with a written summary for your files.Opens at the Volume tier and up
Monthly Chemist Office HoursA live monthly group session on supply, storage and documentation questions, with a recording library for the months you miss.Coming soon
Request a demo with Dr. HopkinsJoin the waitlist for a live demonstration with Dr. Janine Hopkins, our clinical advisor, on applicator workflow, sterile technique and staff education. Demos are scheduled in the order members join.Waitlist open to approved members
IND and research readiness
An IND readiness center gives practices a structured path into research
Guides and templates for the paperwork an investigational study requires, cited to FDA sources and reviewed by counsel before release.
IND 101 for clinicsHow an investigational new drug application works for a practice: sponsor and investigator roles, 21 CFR 312, the forms, the pre-IND meeting, IRB selection and expanded access, with a timeline built from official sources.Coming soon
Research documentation templatesEditable Word templates for the paperwork a study runs on, reviewed by counsel and framed for research use.Coming soon
CMC support packThe supplier documentation an IND submission draws on, gathered in one place, with a request flow for a letter of authorization to reference a master file where one exists.Coming soon
IND readiness checklist and timeline estimatorCheck where your practice stands against each step of an IND and see how long the remaining steps usually take.Coming soon
Science library
The science library turns published research into briefs you can read in minutes
Curated papers per compound, weekly briefs and a regulatory tracker, every entry tied to a peer-reviewed or official source.
Research VaultCurated peer-reviewed literature for each catalog compound, with a printable two-minute brief, evidence at a glance and the papers to start with.Open to approved members
Weekly Evidence Briefs and Research DigestA short weekly brief on newly published research, and a monthly digest by email for members who opt in.Coming soon
Full-text paper libraryOpen-access papers under Creative Commons licenses, hosted in the portal so you can read them in full without leaving.Coming soon
Members Regulatory TrackerFDA bulk substance lists, advisory committee activity and state laws in one tracker, with alerts on the topics you choose.Coming soon
Technical documents
Technical documents show members how to read and verify what arrives
Annotated certificates, data sheets and characterization checklists, written to be useful whoever you buy from.
Annotated COA ReaderSpecimen certificates of analysis you can click through line by line, with what each test establishes, what to check on the page and what to ask your supplier.Open to approved members
Technical data sheetsOne sheet per product family on characterization methods, storage, thaw and handling, cold chain and stability.Coming soon
MISEV2023 characterization checklistThe reporting points of the MISEV2023 guidelines as a checklist you can hold any extracellular vesicle documentation against.Coming soon
Practice operations toolkit
An operations toolkit keeps your supply records audit-ready
Templates, trackers and guides for receiving, storage, supplier qualification and recordkeeping.
Compliance Binder KitEditable templates for the quality binder a practice keeps on its supply: receiving, storage and documentation records.Open to approved members
Supplier ScorecardPut the same ten questions to every supplier you are considering, record what each one documents, and compare up to three side by side before a first order.Open to approved members
Supplier due-diligence checklistOnce you have chosen a supplier, qualify it before a first order: sixteen items from licensure to vesicle composition, with what acceptable evidence looks like, the exact request to send and what to file in your binder. The Scorecard helps you choose; this checklist keeps the record.Open to approved members
Inventory, lot and expiry trackerTrack what is on your shelf by lot and expiry date, and plan reorders against the par levels you set.Coming soon
Cold-chain excursion checkerEnter what your temperature log shows and see the steps to document an excursion and when to contact us.Coming soon
FDA bulk substance lookupLook up where a substance sits on the FDA bulk drug substance lists for compounding, with the date and source of each listing.Coming soon
Patient communication rules guideWhat FTC and FDA rules say about how products are described to patients, quoted from the official sources.Coming soon
Medical director and CPOM packA members guide to medical director arrangements and the corporate practice of medicine doctrine, with agreement checklists reviewed by counsel.Coming soon
Lot and change noticesLot changes, new certificates of analysis and format changes, posted in the portal and sent to you by email.Coming soon
Training and recognition
Training and recognition show patients your practice documents its supply
Workflow modules for your team, a documentation course with a website badge, and early access for Elite partners.
Application workflow trainingShort modules for your team on supply, storage, handling and documentation workflows.Coming soon
Documentation course and Verified Practice badgeComplete the documentation course to earn a Verified ExaVeyra Practice badge for your website, linked to your listing in our practitioner directory.Coming soon
Office Hours question archiveEvery member question answered in Office Hours, searchable, with no patient information.Coming soon
Early access to new formatsSee new formats and collections before they open to the wider network, with a "New this month" list in the library.Coming soon. Opens at the Elite tier and up
A chemist can walk you through the network before you register
Book a short call to ask what the network holds for your practice, how verification works or what a resource covers. The call is about supply, storage and documentation.