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Mhra Clinical Trial Portal

Link van Mhra Clinical Trial Portal pagina wordt hieronder gegeven. Pagina's met betrekking tot Mhra Clinical Trial Portal worden ook vermeld.

Laatst bijgewerkt: 2022-02-04 11:11:47

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Toegevoegd door: Timothy Sutton

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Clinical trials for medicines: apply for ... - GOV.UK

18-12-2014 · Clinical trials can also be ... you should email this to the MHRA at [email protected] with subject line “Clinical Trial Registration ... The IRAS portal includes a list of ...
Url: https://www.gov.uk/guidance/clinical-trials-for-medicines-apply-for-authorisation-in-the-uk
Clinical trials for medicines: apply for ... - GOV.UK

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Toegevoegd door: Chao Xu

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Clinical trials for medicines: manage your ... - GOV.UK

18-12-2014 · Call the MHRA’s Clinical Trials Unit on 020 3080 6456 to discuss the issue with a medical ... To gain access to the MHRA Gateway you need to register to another portal called MHRA Submissions.
Url: https://www.gov.uk/guidance/clinical-trials-for-medicines-manage-your-authorisation-report-safety-issues
Clinical trials for medicines: manage your ... - GOV.UK

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Toegevoegd door: Niels Walter

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Register to make submissions to the MHRA - GOV.UK

31-12-2020 · Clinical trial applicants - this is the first 5 digits of the CTA number from a trial that your organisation has previously submitted. This can …
Url: https://www.gov.uk/guidance/register-to-make-submissions-to-the-mhra
Register to make submissions to the MHRA - GOV.UK

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Toegevoegd door: Kyla Geen

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MHRA Portal: register to submit forms - GOV.UK

Url: https://www.gov.uk/guidance/mhra-portal-register-to-submit-forms
MHRA Portal: register to submit forms - GOV.UK

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Toegevoegd door: Stephen Thirgood

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Notify the MHRA about a clinical investigation ... - GOV.UK

18-12-2014 · If possible, please provide the MHRA with advanced notice of your intention to submit a clinical investigation by emailing [email protected] with some basic details about the ...
Url: https://www.gov.uk/guidance/notify-mhra-about-a-clinical-investigation-for-a-medical-device
Notify the MHRA about a clinical investigation ... - GOV.UK

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Toegevoegd door: Steven Sashen

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Submitting via MHRA Submissions portal - GOV.UK

Submitting via MHRA Submissions portal. 2 OFFICIAL Agenda Item Intro The MHRA ... MHRA Submissions • 1 webform, ~10 fields .zip file ... SFTP from Day 1. 15 OFFICIAL Clinical Trial applications All clinical trial applications types will be submitted via this Human Medicines tile. Please note - For all new clinical trial submissions ...
Url: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/948876/Technical_Guidance_-_Submitting_via_MHRA_Submissions_SL__002_.pdf
Submitting via MHRA Submissions portal - GOV.UK

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Toegevoegd door: Fiona Dimas-herd

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MHRA announces streamlined clinical trial review process

16-07-2021 · MHRA announces streamlined clinical trial review process. In the wake of the systemic changes flowing from the UK’s exit from the EU, the country’s Medicines and Healthcare products Regulatory Agency (MHRA) plans to streamline review of clinical trials for medicinal products. Beginning in January 2022, new Clinical Trials of Investigational ...
Url: https://www.raps.org/news-and-articles/news-articles/2021/7/mhra-announces-streamlined-clinical-trial-review-p
MHRA announces streamlined clinical trial review process

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Toegevoegd door: Johnny Lam

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Contact MHRA - GOV.UK

09-04-2020 · If you are checking the status of a clinical trial submission, ... For enquiries about registering and submitting product licence applications using MHRA portal. Telephone: 020 …
Url: https://www.gov.uk/guidance/contact-mhra
Contact MHRA - GOV.UK

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Toegevoegd door: Jimmy Baldo

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New proposals for the future of UK clinical trial legislation

17-01-2022 · The MHRA is an executive agency of the Department of Health and Social Care. The current UK legislation, The Medicines for Human Use (Clinical Trials) Regulations 2004, as amended, transposed the ...
Url: https://www.gov.uk/government/news/new-proposals-for-the-future-of-uk-clinical-trial-legislation
New proposals for the future of UK clinical trial legislation

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Toegevoegd door: European Medicines Agency

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Implementation of the clinical trials regulation

Implementation of the clinical trials regulation

Toegevoegd door: MMS Holdings

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New EU Clinical Trials Regulation: What’s New?

New EU Clinical Trials Regulation: What’s New?

Toegevoegd door: MHRAgovuk

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EU Exit and post-transition guidance, clinical trials webinar - October 2020

EU Exit and post-transition guidance, clinical trials webinar - October 2020

Toegevoegd door: Ergomed plc

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Webinar: BREXIT – Impact on Clinical Trials Being Run in the UK

Webinar: BREXIT – Impact on Clinical Trials Being Run in the UK

Toegevoegd door: Prof.Karan Ajay Gupta

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MHRA BRITAIN I Medicines and Healthcare products Regulatory Agency

MHRA BRITAIN I Medicines and Healthcare products Regulatory Agency

Toegevoegd door: ePharmaSolutions

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Clinical Trial Portal

Clinical Trial Portal

Toegevoegd door: MHRAgovuk

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EU Exit and post-transition guidance, Regulation of Medical Devices Webinar - October 2020

EU Exit and post-transition guidance, Regulation of Medical Devices Webinar - October 2020

Toegevoegd door: GCP-Mindset - All About Clinical Research

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Regulatory Authority Inspections in Clinical Trials - FDA and MHRA - Part 3

Regulatory Authority Inspections in Clinical Trials - FDA and MHRA - Part 3

Toegevoegd door: MHRAgovuk

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Post Transition: Pharmacovigilance Requirements for UK Authorised Products - October 2020

Post Transition: Pharmacovigilance Requirements for UK Authorised Products - October 2020

Toegevoegd door: MHRAgovuk

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MHRA Board Meeting held in public April 2022

MHRA Board Meeting held in public April 2022
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