Legal

Terms and Conditions

Version [v0.1-draft] · Effective [To be confirmed] · Draft date 13 August 2026

PTP-102 Portal — Legal and Commercial Terms Addendum. Jurisdictional focus: Ireland and the European Union. Status: non-lawyer working draft for review by qualified Irish/EU counsel before publication or sale.

00

Summary at a glance

This document sets out the legal and commercial terms proposed for access to the PTP-102 portal, including paid company access, the Business Access Window, the three-month reservation product, confidentiality, data protection, and liability.

  • • Portal access is conditional on vetting, approval, NDA, and acceptance of the applicable terms.
  • • Payment buys a limited, revocable right of access — not ownership, a licence, or a guaranteed transaction.
  • • The Business Access Window is a US$1,020 paid, time-limited route by which a fully vetted, NDA-bound company may access the clinical trial portal for an approved business-evaluation purpose. It is personal to that company, non-transferable, revocable, and separate from the three-month reservation.
  • • The three-month reservation confers only the review or priority right written in the order form; exclusivity applies only if the order form says so.
  • • Commercial terms live here; personal-data handling is described in the Privacy Policy.
  • • Liability is capped by contract, subject to Excluded Claims and mandatory law.

Important: This document is not legal advice and is not a substitute for a written opinion from Irish counsel, the trial sponsor, the data controller(s), or any other competent regulatory adviser. It is a structured working draft intended to help counsel and Base44 implement the correct contract and privacy boundaries.

Change history

  • • 13 August 2026 — Added the “Business Access Window” subsection at clause 10 of the Portal Access and Commercial Terms, incorporating the US$1,020 access fee, and renumbered the following clauses (reservation schedule is now clause 11).
  • • 13 August 2026 — Updated the summary, executive conclusion, working assumptions, implementation checklist, and counsel-confirmation checklist to distinguish the US$1,020 Business Access Window from the separate US$2,500 three-month reservation.

Version [v0.1-draft] and effective date [To be confirmed] are unchanged; the document remains a non-lawyer working draft pending counsel review.

01

Executive conclusion

1.1 Paid company access

Charging a vetted company for controlled access to a live trial-data or licensing portal is not automatically unlawful. It can be structured as a paid data-room, evaluation, diligence, or licensing service. The payment, NDA, company vetting, and server-side access controls are useful risk controls, but they do not by themselves prove that the provider is entitled to disclose every item in the portal.

Before access is sold, the provider should be able to demonstrate:

  • • authority from the trial sponsor, owner, clinic, investigator, or other rights-holder to disclose the relevant materials;
  • • compliance with any veterinary clinical-trial, protocol, sponsor, ethics, informed-consent, confidentiality, and pharmacovigilance restrictions that apply to the underlying study;
  • • a documented data map showing which records are personal data, confidential information, trade secrets, regulated records, or third-party material;
  • • appropriate redaction or pseudonymisation, a lawful data-protection basis, and written processor/controller arrangements where required;
  • • access limited to the approved company, named users, territory, purpose, tier, and time period; and
  • • a contract that says exactly what is being bought and what is not being promised.

1.2 Business Access Window (US$1,020)

The Business Access Window is the paid, controlled route by which an eligible company may obtain time-limited access to the PTP-102 clinical trial portal for a fee of US$1,020. It should be documented as a paid access and evaluation service, on the same basis as paragraph 1.1: the fee, the NDA, the vetting, and the server-side controls are risk controls, not evidence of a right to disclose every item exposed during the window.

Payment must not create ownership, a licence to the underlying intellectual property, an entitlement to acquire or commercialise PTP-102, or any guarantee of a transaction, partnership, exclusivity, regulatory outcome, or continued access. The access window is personal to the approved company and its specifically authorised representatives, is not transferable, and is revocable. The Business Access Window and the three-month reservation described below are separate products with separate fees and separate legal effects, and must never be described as one offer.

TODO: Counsel or commercial confirmation required — window duration, commencement trigger, refund and cancellation rules, renewal basis, currency and tax treatment, and the precise Portal areas included.

1.3 Three-month paid reservation / holding option

The proposed US$2,500 product should be treated as a separate commercial reservation or term-sheet review service, not as an automatic licence, ownership transfer, guaranteed exclusivity, or promise that a transaction will close.

The current project context indicates that the offer is intended to reserve a requested territory for up to three months of exclusive term-sheet review, while also describing the opportunity as limited and non-exclusive in places. Those descriptions must be reconciled before publication. The contract should state whether the buyer receives:

  1. no exclusivity, only a priority review period;
  2. limited exclusivity for a precisely defined territory and field of use; or
  3. a different negotiated right recorded in an individual order form.

The safest default is limited priority review, with exclusivity only if the order form expressly says so.

1.4 Privacy Policy versus Terms and Conditions

Commercial terms should be placed in a Terms and Conditions / Portal Access Agreement and, for the US$2,500 product, a short Reservation and Term-Sheet Schedule or order form.

The Privacy Policy should explain how personal data is handled. It should not be used as the main place for price, refunds, exclusivity, licence scope, reservation rights, warranties, or liability caps.

1.5 Liability cap

There is no general Irish/EU rule that makes the provider legally safe merely because liability is capped at €100 or US$100. A cap is a contractual risk-allocation term, not a ban on bringing a claim. It must be transparent, properly accepted, and reviewed against mandatory law, consumer status, negligence, fraud, confidentiality, data protection, intellectual-property misuse, and any regulatory obligations.

Do not publish wording such as “the customer may not take legal action for claims below €100.” Use a conventional liability-cap clause instead, with counsel selecting the currency and carve-outs.

02

Working assumptions requiring confirmation

These assumptions are taken from the existing PTP-102 project materials and must be confirmed against the authoritative seller, sponsor, and product records:

  • • The portal operator is intended to be Byrock Technologies Ltd, or another legal entity that must be named in the final contract.
  • • Companies are expected to be vetted, approved, and subject to NDA and access controls before protected access is granted.
  • • Portal roles include company_lead, company_member, clinical_investigator, consultant, and platform_admin; these must remain separate server-side roles.
  • • Two distinct paid commercial products are described: a US$1,020 Business Access Window giving time-limited portal access to an approved company, and a US$2,500 three-month territory reservation / term-sheet review opportunity. They are not the same product and must not be sold or described interchangeably.
  • • The Business Access Window is intended to be available only to a registered, fully vetted and approved company that has executed the applicable NDA, verified its representatives, and accepted these Terms. Its duration, commencement trigger, refund and renewal rules, currency and tax treatment, and precise access scope are not established by the existing materials (TODO: Counsel or commercial confirmation required).
  • • The reservation is not intended to be a final licence, a transfer of clinical data ownership, or a guaranteed transaction.
  • • The live portal may contain clinical, regulatory, commercial, technical, or personal data, and may include information received from third parties.
  • • Payment is processed through a third-party payment provider. The seller identity, merchant-of-record position, tax treatment, refund workflow, and chargeback handling still require confirmation.

If any assumption is wrong, the addendum must be revised before implementation.

04

Proposed Terms and Conditions Addendum

PTP-102 Portal Access and Commercial Terms

The text below is a Base44-ready working draft. Replace every bracketed item and have counsel approve it before publication.

1.Parties and scope

These Portal Access and Commercial Terms (“Terms”) govern access to the PTP-102 portal and any related data room, evaluation environment, licensing workspace, document centre, or term-sheet workflow (together, the “Portal”) made available by [Provider legal name], a company incorporated in [jurisdiction] with registered address at [address] (“Provider”).

The customer is the legal entity identified in the approved application, order form, or reservation record (“Customer”). An individual user may access the Portal only as an authorised representative or approved member of Customer.

These Terms are supplemented by any signed NDA, Data Processing Addendum, order form, reservation schedule, or other written agreement identified in the Portal. If documents conflict, the more specific signed document controls for that subject matter.

2.Eligibility and approval

Portal access is conditional on successful company and user vetting, email verification, administrator approval, acceptance of the applicable Terms and NDA, and any other approval stated in the order form. Provider may refuse, suspend, or revoke access where information is incomplete, inaccurate, misleading, expired, or inconsistent with the approved purpose.

Customer must ensure that each user is authorised, uses a unique account, protects credentials, and immediately reports suspected compromise or unauthorised access. Customer is responsible for its users and representatives.

3.Limited access right

Subject to payment, approval, and continued compliance, Provider grants Customer a limited, non-transferable, non-sublicensable, revocable right to access the specific Portal areas and materials listed in the applicable order form, solely for the approved evaluation, diligence, regulatory, or licensing purpose.

No access right is granted by implication. Customer receives no ownership or general licence to the Portal, software, database, clinical records, regulatory submissions, trade secrets, documents, trademarks, or other intellectual property.

4.Permitted use and prohibited conduct

Customer may use the approved materials only for the stated purpose and only through approved users and representatives with a need to know. Customer must not:

  • • copy, download, scrape, bulk-export, index, publish, sell, or redistribute Portal material except where the order form expressly permits it;
  • • attempt to identify a pseudonymised patient, owner, investigator, or other person;
  • • use the material to compete with Provider or any trial sponsor;
  • • reverse engineer, probe, interfere with, or bypass Portal access controls;
  • • share access with an unapproved affiliate, adviser, competitor, or third party;
  • • use the material to make a clinical, regulatory, investment, or commercial decision without independent professional review; or
  • • use the Portal for an unlawful purpose or in breach of any applicable protocol, law, NDA, or third-party right.

5.Confidentiality

All non-public clinical, technical, regulatory, financial, commercial, operational, and intellectual-property information made available through the Portal is Confidential Information. Customer must protect it using at least reasonable technical and organisational measures and must disclose it only to approved representatives who are bound by confidentiality duties no less protective than these Terms or the applicable NDA.

Customer remains responsible for any breach by its users or representatives. Confidentiality obligations survive suspension or termination. Trade secrets remain protected for so long as they qualify as trade secrets under applicable law; other Confidential Information remains protected for [five years / other counsel-approved period] after disclosure or termination.

6.Data protection

Each party must comply with applicable data-protection law. The parties must document whether each party acts as controller, joint controller, or processor for each processing activity. Where Provider processes personal data on Customer’s documented instructions, the parties must execute an appropriate Data Processing Addendum before that processing begins.

Customer must not upload personal data, special-category data, credentials, payment data, or restricted clinical records unless the order form and written instructions expressly permit it and the required legal basis, notices, permissions, security controls, and data-processing agreement are in place.

Provider may process account, identity, access, payment, audit, support, and security data to operate, secure, administer, and improve the Portal, subject to the Privacy Policy and applicable law.

7.Clinical and regulatory disclaimer

The Portal is an information and commercial evaluation environment. It is not a substitute for veterinary care, a clinical decision, a regulatory submission, legal advice, investment advice, or independent due diligence. Unless a written agreement expressly states otherwise, Provider does not warrant that Portal material is complete, current, error-free, suitable for a particular purpose, approved by a regulator, or sufficient to support a licence or transaction.

Customer must make its own legal, scientific, regulatory, financial, and commercial assessment.

8.Intellectual property and database use

Provider and its licensors retain all rights in the Portal and its content. Customer receives only the limited access right expressly stated in the applicable order form. Customer must preserve notices, watermarks, attribution, and access controls and must not extract or reutilise a substantial part of the Portal database or systematically extract/reutilise insubstantial parts in a way that conflicts with the permitted purpose.

9.Fees and payment

Fees, currency, taxes, payment timing, and any included services are stated in the applicable order form. Access may remain suspended until payment has cleared and all approval gates are complete. Customer is responsible for applicable taxes unless the order form states otherwise.

Payment of a fee does not itself create a licence, exclusivity, regulatory approval, ownership right, or obligation to complete a transaction. The Business Access Window in clause 10 and the three-month reservation in clause 11 are separate products with separate fees and separate legal effects.

10.Business Access Window

Where the order form identifies the product as a “Business Access Window”, Provider makes available a paid, controlled, time-limited route by which an eligible Customer may access the PTP-102 clinical trial portal for the approved business-evaluation purpose, for a fee of US$1,020. The Business Access Window is a distinct commercial product from the three-month reservation / term-sheet review described in clause 11: the Business Access Window buys access only, while the reservation buys the review, priority, or negotiation right written in the order form. Neither product confers a licence, ownership, exclusivity, or a guaranteed transaction, and buying one does not include or imply the other.

A Business Access Window may be granted only to a Customer that has completed company registration and vetting, administrator approval, identity verification of its authorised representatives, execution of the applicable NDA, and acceptance of the applicable version of these Terms, as required by clauses 2 and 3. Access remains subject to clauses 4 to 8 in full, including permitted use, confidentiality, data protection, the clinical and regulatory disclaimer, and intellectual-property and database use. Personal data processed in connection with the Business Access Window is handled as described in the Privacy Policy; confidentiality, Portal-use restrictions, NDA obligations, and the commercial access conditions are governed by these Terms and not by that policy.

#ItemTerm
1FeeCustomer shall pay US$1,020 for one Business Access Window. Currency of charge, tax treatment, and whether the amount is stated inclusive or exclusive of VAT or other taxes are not confirmed by the existing source material. TODO: Counsel or commercial confirmation required.
2What the fee buysThe fee buys a limited, conditional, revocable right of access to the authorised Portal areas for the approved business-evaluation purpose. It does not buy ownership, an intellectual-property or commercial licence, exclusivity, an option or right to acquire or commercialise PTP-102, a partnership, a regulatory outcome, a guaranteed transaction, or a right to continued access.
3Recurring or one-timeWhether the Business Access Window is a one-time charge or renews, and on what basis, is not confirmed by the existing source material. TODO: Counsel or commercial confirmation required.
4Effective dateAccess is activated only after payment has cleared, Provider has accepted the order, and the company vetting, identity-verification, NDA, and Terms-acceptance gates in clauses 2 and 3 are complete. The precise commencement trigger recorded in the order form is not confirmed. TODO: Counsel or commercial confirmation required.
5DurationThe Business Access Window is time-limited. The length of the window is not confirmed by the existing source material and must be stated in the order form. TODO: Counsel or commercial confirmation required.
6Access scopeAccess is confined to the Portal areas and materials listed in the applicable order form and to the approved business-evaluation purpose. Any read-only, export, download, or watermark restriction applying to those areas must be stated in the order form. The precise access scope is not confirmed. TODO: Counsel or commercial confirmation required.
7Personal to CustomerAccess is personal to the approved Customer and its specifically authorised representatives. It may not be transferred, assigned, shared, sublicensed, resold, or exercised by or for an undisclosed third party, affiliate, adviser, or competitor.
8Prohibited useClause 4 applies in full. Downloading, scraping, bulk extraction, indexing, redistribution, publication, reverse engineering, unauthorised copying, and use of information outside the approved purpose are prohibited.
9Suspension and terminationProvider may suspend or terminate a Business Access Window under clause 11, including for a security concern, a breach of these Terms or the NDA, inaccurate or misleading application information, unauthorised use, legal or regulatory necessity, or risk to trial integrity, confidentiality, intellectual property, or data protection.
10Cancellation and refundsWhether the fee is refundable, partially refundable, or non-refundable, and the applicable cancellation route, are not confirmed by the existing source material. TODO: Counsel or commercial confirmation required.
11ExpiryAccess ends automatically at the end of the window unless extended in writing. Expiry does not create a continuing right of access, exclusivity, licence, or entitlement to a transaction, and does not end the confidentiality obligations in clause 5.

11.Three-month reservation / term-sheet review schedule

Where the order form identifies the product as a “Three-Month Reservation”. This product is separate from, and is not included in, the Business Access Window in clause 10:

#ItemTerm
1FeeCustomer shall pay [US$2,500 / other confirmed amount] in the currency shown in the order form.
2Effective dateThe reservation starts only when payment has cleared, Provider has accepted the order, and the required company, NDA, and legal approval gates are complete.
3TermThe reservation lasts three months from the Effective Date, unless ended earlier under these Terms or the order form.
4Territory and fieldThe reserved territory and field of use must be stated precisely as [insert territory] and [insert field of use]. A reservation has no effect outside that description.
5Nature of rightThe reservation gives Customer only the review, access, priority, or negotiation right expressly written in the order form. It is not a licence, an option to purchase, a transfer of ownership, a guarantee of regulatory approval, or a promise that a definitive agreement will be signed.
6ExclusivityThere is no exclusivity unless the order form expressly marks the reservation as “exclusive” and defines the affected territory, field, product, and prohibited competing commitments. Any exclusivity is limited to that definition and duration and is subject to existing rights, mandatory law, and Provider’s ability to perform lawfully.
7No automatic transactionProvider may decline a proposed transaction following legal, regulatory, scientific, technical, commercial, sanctions, diligence, or counterparty review. Customer must not represent that it owns or controls the reserved territory or product.
8Refund choice[Choose one after counsel review: (a) full refund if Provider cannot lawfully provide the stated reservation; (b) pro-rata refund for unused time after Provider breach; (c) no refund after access begins except for Provider’s material breach or mandatory law.]
9Credit choiceThe fee is [not credited / credited in whole / credited in part] against a later signed licence or transaction only if the later written agreement says so.
10ExpiryThe reservation ends automatically at the end of the three-month term unless extended in writing. Expiry does not create a continuing exclusivity, licence, or right to a transaction.

12.Suspension and termination

Provider may suspend or terminate access immediately where necessary to protect security, comply with law, respond to a regulator or rights-holder, address a breach, or prevent unauthorised disclosure. Provider may also terminate for material breach not cured within [ten] business days after notice, unless immediate action is justified.

On termination or expiry, Customer must stop using the Portal, return or securely delete Confidential Information as directed, and ensure that its representatives do the same, subject to legally required archival retention.

13.Liability and exclusions

This section applies only to the extent permitted by applicable law and must be reviewed for each customer type.

Option A — fixed B2B cap

For a Customer acting solely in the course of business, and excluding the Excluded Claims below, Provider’s aggregate liability arising out of or relating to the Portal, access, a Business Access Window, or a reservation shall not exceed [€100 / US$100].

Option B — fee-linked B2B cap

For a Customer acting solely in the course of business, and excluding the Excluded Claims below, Provider’s aggregate liability arising out of or relating to the Portal, access, a Business Access Window, or a reservation shall not exceed the greater of [€100 / US$100] and the fees paid by Customer for the affected service during the twelve months before the event giving rise to the claim.

“Excluded Claims” means liability that cannot lawfully be excluded or limited, including any category that counsel identifies as mandatory under applicable law, and may include fraud or fraudulent misrepresentation, death or personal injury caused by negligence, deliberate misconduct, unpaid refund or payment obligations, and specified breaches of confidentiality, data protection, or intellectual-property rights.

To the extent permitted by law, neither party is liable for indirect or consequential loss, loss of profit, revenue, business opportunity, anticipated savings, goodwill, or reputation. This does not remove a mandatory statutory right or prevent a regulator, court, or competent authority from exercising its powers.

14.Governing law and disputes

Subject to mandatory rights and any different written agreement, these Terms are governed by the laws of Ireland and the parties submit to the courts of Ireland. Counsel must confirm whether this clause is appropriate for each customer’s jurisdiction and whether any mandatory local law applies.

15.Electronic acceptance and version control

Customer accepts these Terms by an affirmative action after being given a reasonable opportunity to read and save them. Provider will retain the accepted version, timestamp, user, company, and related approval records. A later version applies only after the required notice and re-acceptance process.

05

Recommended Privacy Policy changes

Add a commercial-portal section to the Privacy Policy, but keep commercial promises in the Terms. The Privacy Policy should describe:

  • • account, identity, company, role, vetting, verification, and representative data;
  • • payment, billing, tax, refund, fraud-prevention, and chargeback data;
  • • access, download, export, security, device, IP, user-agent, and audit-log data;
  • • purposes and lawful bases for onboarding, access control, contract performance, security, support, compliance, and dispute handling;
  • • the role of the Provider and any sponsor, clinic, investigator, company customer, payment provider, hosting provider, analytics provider, and support provider;
  • • retention periods or retention criteria;
  • • international transfers and safeguards;
  • • data-subject rights and contact routes;
  • • incident and breach handling at a high level; and
  • • cookies or similar technologies used by the Portal.

The Privacy Policy should expressly say that the provider does not invite users to upload credentials, API keys, payment-card data, webhook secrets, or restricted clinical records unless a separate approved workflow says otherwise.

06

Data that should remain non-public by default

Do not expose the following to prospective companies unless a documented approval specifically permits it:

  • • direct owner contact details, personal addresses, phone numbers, or email addresses;
  • • identifiable patient, investigator, or clinic information where not necessary for the approved purpose;
  • • raw informed-consent forms, signatures, identity documents, or unredacted regulatory correspondence;
  • • credentials, API keys, webhook secrets, payment-card data, access tokens, or security configuration;
  • • internal administrator notes, approval queues, audit-chain internals, or other users’ audit histories;
  • • data supplied under a sponsor, clinic, investigator, vendor, or third-party confidentiality restriction;
  • • unapproved exports of clinical records or adverse-event material; and
  • • any data that the provider cannot trace to a lawful disclosure right.
07

Base44 implementation checklist

Access and agreements

  • Require approved company status before paid or protected access.
  • Require an identified company lead and separately approved members.
  • Require NDA acceptance or countersignature before confidential-data access.
  • Require the relevant Terms version and the applicable Business Access Window or reservation schedule to be accepted before access starts.
  • Keep the US$1,020 Business Access Window and the US$2,500 three-month reservation as separate purchasable products with separate records, entitlements, and expiry handling.
  • Keep company, consultant, investigator, and admin routes separate server-side.
  • Revoke access automatically at expiry, suspension, termination, or failed payment where appropriate.

Commercial workflow

  • Display the seller’s verified legal name, registered address, currency, taxes, and payment provider.
  • Replace mixed “exclusive” and “non-exclusive” copy with one counsel-approved definition.
  • Store territory, field of use, term, start date, expiry date, refund rule, credit rule, and exclusivity flag as structured fields.
  • Store the Business Access Window product code, fee, activation date, expiry date, authorised representatives, and permitted Portal areas as structured fields, and expire access automatically at the end of the window.
  • Do not grant a licence or imply a completed transaction when payment only buys reservation or review.
  • Provide a clear refund and cancellation path that matches the payment-provider configuration.
  • Prevent a payment-success event from bypassing legal, vetting, or data-access gates.

Data and security

  • Complete a data inventory and controller/processor map.
  • Redact or pseudonymise personal and restricted clinical data before company access.
  • Add export, download, watermark, and representative controls where required.
  • Log acceptance, access grants, exports, downloads, sharing, suspension, revocation, and failed permission decisions.
  • Verify hosting, support, analytics, and payment-provider data locations and transfer safeguards.
  • Keep secrets, credentials, payment data, and restricted clinical records outside the commercial data room.
08

Counsel confirmation checklist

Obtain written confirmation on each item before publication:

  1. Correct contracting entity, registered address, signatory authority, and merchant-of-record identity.
  2. Rights from the trial sponsor, owner, investigator, clinic, or other data/licence holder to disclose each category.
  3. Whether any proposed data is subject to veterinary clinical-trial authorisation, protocol, GCP, pharmacovigilance, ethics, or informed-consent restrictions.
  4. GDPR controller/processor/joint-controller roles and whether a DPA, DPIA, or additional notice is required.
  5. Redaction, pseudonymisation, retention, export, and international-transfer design.
  6. Whether the intended customer population is exclusively B2B and how consumer-facing edge cases are excluded or handled.
  7. Whether the US$2,500 payment is a service fee, reservation fee, deposit, option fee, or credit, and its VAT/tax treatment.
  8. Whether the US$1,020 Business Access Window fee is a service or access fee, its currency, VAT/tax treatment, and whether it is one-time or recurring.
  9. The Business Access Window duration, commencement trigger, renewal basis, cancellation and refund rules, and the precise Portal areas and read-only or export restrictions included.
  10. Exact refund, cancellation, failed-delivery, chargeback, and transaction-credit rules.
  11. Exact meaning of “exclusive,” including territory, field, product, existing commitments, and competition-law review.
  12. Choice of governing law, courts, dispute process, and mandatory local-law issues.
  13. Liability-cap option, currency, amount, exclusions, and any indemnity wording.
  14. NDA duration, trade-secret treatment, return/destruction process, and remedies.
  15. Electronic-acceptance and audit-record requirements, including retention and evidential use.
  16. Whether separate sponsor, licensee, data-room, reservation, or order-form documents are required instead of one portal addendum.
09

Sources and reference points

The following primary or official materials informed this working draft. Counsel should confirm the current consolidated versions and any sector-specific Irish guidance before publication.

10

Project-source note

The commercial assumptions in this draft come from the existing PTP-102 project materials, including the role-path specification, NDA workflow, portal access model, the working description of the US$2,500 three-month reservation, and the US$1,020 Business Access Window. Those materials are product context, not independent proof of legal title, regulatory approval, seller identity, or enforceability. They must be replaced or confirmed by authoritative documents before the offer goes live.

11

Not legal advice

This document is not legal advice and is not a substitute for a written opinion from Irish counsel, the trial sponsor, the data controller(s), or any other competent regulatory adviser. It is a structured working draft intended to help counsel and Base44 implement the correct contract and privacy boundaries.

Questions about these terms?

Contact us, or review how personal data is handled in the Privacy Policy.

Cookies & privacy

We use strictly necessary cookies to operate the site and, with your consent, analytics and functional cookies. You can accept all, reject all, or manage your preferences. Non-essential trackers are blocked until you consent.