Monday, February 16, 2026 3:53:21 PM
I dont believe there would be any need for this hire to oversee privately run clinics too. There is no regulation in the UK (under the ATMP framework) that forbids companies from using third-parties for cell collection so I dont reckon the MHRA would mandate that NWBO have to have QMS oversight of privately run clinics simply for Leukapheresis.
Having said that, there is a nuance here. A leukapheresis centre must hold a Human Tissue Authority (HTA) Licence as the HTA regulates the collection of human cells intended for human application. Now a satellite facility of Advent can piggyback on Advent's existing HTA licence having had due inspections. But a satellite facility would also require an entirely new CQC (Care Quality Commission) certification, which must be obtained before the first patient can be treated. Furthermore, - and herein lies a substantial hurdle to servicing NHS England patients with this facility, - the facility would also require an entirely new JACIE certification, which cannot be obtained until the facility has been operational for at least 12 months (and is mandatory in order to begin servicing NHS patients).
So, based on this, this satellite would only be able to service private patients (and compassionate use & I suppose new trial patients) once the HTA and CQC are received. Thereafter 12 months of private collections would be needed to generate the SOP required to apply for the JACIE Certification. Once received, then the facility can service NHS patients. So, it seems the timeline looks something like this:
Phase 1 (Months 0-6): Fit out the clinic. Secure CQC registration & HTA Satellite status.
Phase 2 (Month 6-18): Open for Private patients & Compassionate Use/ Trial participants only. Use these patients to generate the data and SOP proof required for JACIE.
Phase 3 (Month 18+): Apply for and achieve JACIE accreditation. Once achieved begin servicing NHS-funded patients efficiently.
From what I have read this JACIE certification unfortunately cannot be sidestepped or fast-tracked if the intended end use of this facility is to include NHS patients.
Having said that, there is a nuance here. A leukapheresis centre must hold a Human Tissue Authority (HTA) Licence as the HTA regulates the collection of human cells intended for human application. Now a satellite facility of Advent can piggyback on Advent's existing HTA licence having had due inspections. But a satellite facility would also require an entirely new CQC (Care Quality Commission) certification, which must be obtained before the first patient can be treated. Furthermore, - and herein lies a substantial hurdle to servicing NHS England patients with this facility, - the facility would also require an entirely new JACIE certification, which cannot be obtained until the facility has been operational for at least 12 months (and is mandatory in order to begin servicing NHS patients).
So, based on this, this satellite would only be able to service private patients (and compassionate use & I suppose new trial patients) once the HTA and CQC are received. Thereafter 12 months of private collections would be needed to generate the SOP required to apply for the JACIE Certification. Once received, then the facility can service NHS patients. So, it seems the timeline looks something like this:
Phase 1 (Months 0-6): Fit out the clinic. Secure CQC registration & HTA Satellite status.
Phase 2 (Month 6-18): Open for Private patients & Compassionate Use/ Trial participants only. Use these patients to generate the data and SOP proof required for JACIE.
Phase 3 (Month 18+): Apply for and achieve JACIE accreditation. Once achieved begin servicing NHS-funded patients efficiently.
From what I have read this JACIE certification unfortunately cannot be sidestepped or fast-tracked if the intended end use of this facility is to include NHS patients.
Recent NWBO News
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 04/21/2026 04:15:08 AM
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 04/16/2026 09:25:30 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/07/2026 04:30:50 PM
- Form NT 10-K - Notification of inability to timely file Form 10-K 405, 10-K, 10-KSB 405, 10-KSB, 10-KT, or 10-KT405 • Edgar (US Regulatory) • 03/31/2026 09:04:37 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/15/2026 10:06:20 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/02/2026 10:14:59 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/28/2025 09:43:27 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/25/2025 10:23:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/20/2025 09:26:03 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 11/19/2025 09:15:48 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:44:21 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/31/2025 04:29:10 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/30/2025 08:40:05 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/24/2025 04:28:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/14/2025 06:22:26 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2025 09:00:38 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 07/01/2025 09:04:38 PM
