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Mhra Portal Guidance

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

Laatst bijgewerkt: 2022-02-04 20:38:47

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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: Murray Rogan

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New guidance and information for industry from the MHRA

01-01-2021 · The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK’s standalone medicines and medical devices regulator. The below guidance should be followed from 1 January 2021.
Url: https://www.gov.uk/government/collections/new-guidance-and-information-for-industry-from-the-mhra
New guidance and information for industry from the MHRA

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Toegevoegd door: Tony Phelps

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Guidance - Medicines and Healthcare products Regulatory Agency

Medicines and Healthcare products Regulatory Agency (MHRA) - Falsified Medicine Directive. Application and management of Wholesale Dealer's Authorisation "WDA(H)" and Active Pharmaceutical Ingredients "API"
Url: https://pclportal.mhra.gov.uk/guidance/
Guidance - Medicines and Healthcare products Regulatory Agency

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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 Submissions homepage ... PIPs MHRA Submissions 5 webforms available .PDF file, .zip file, unstructured documents No No 1. ... • These steps and guidance are found here: https: ...
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: Niels Walter

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Register to make submissions to the MHRA - GOV.UK

31-12-2020 · Please use the following guidance with regards to ICSR reporting unless communications from the MHRA advise otherwise. Business Continuity Plan ( PDF , 15.8KB , 2 pages ) Where to go for help
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: Sydney Stevenson

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Guidance on submitting clinical trial safety reports - GOV.UK

31-12-2020 · The reference guide Gaining Access to MHRA Submissions provides a step-by-step account of how to set up user access. Guidance on managing users of the portal is also available in the reference ...
Url: https://www.gov.uk/guidance/guidance-on-submitting-clinical-trial-safety-reports
Guidance on submitting clinical trial safety reports - GOV.UK

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Toegevoegd door: Satill & Miller Services Pty. Limited

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MHRA baseline guidance - GOV.UK

MHRA baseline guidance . A baseline submission refers to submission of all current valid documents along with a statement that the content has not changed, ... Baselines submitted through the portal should be submitted as Information updates . Once switched from NeeS to eCTD it is not possible to return to NeeS .
Url: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/480354/MHRA_baseline_guidance.pdf
MHRA baseline guidance - GOV.UK

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Toegevoegd door: Tim Mooney

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MHRA Portal - Medicines and Healthcare products Regulatory ...

View the Terms & Conditions of use for the MHRA Portal ...
Url: https://info.mhra.gov.uk/mhra_portal.aspx
MHRA Portal - Medicines and Healthcare products Regulatory ...

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Toegevoegd door: William Suganda

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MHRA Submissions – The UK submissions ... - S-cubed Global

04-12-2020 · This new MHRA submissions portal will also apply to submissions relating to e-cigarettes, brokers of medicinal products and Active Substance Master Files (ASMF) holders, so these activities will also require registration and access to MHRA Submissions. ... MHRA Additional Guidance.
Url: https://www.s-cubed-global.com/news/mhra-submissions-the-uk-submissions-portal
MHRA Submissions – The UK submissions ... - S-cubed Global

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Toegevoegd door: MHRAgovuk

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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

Toegevoegd door: Prof.Karan Ajay Gupta

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MHRA BRITAIN I Medicines and Healthcare products Regulatory Agency

Toegevoegd door: MHRAgovuk

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

Toegevoegd door: MHRAgovuk

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E Cigarettes EU Exit and Post Transition Guidance Webinar - November 2020

Toegevoegd door: MHRAgovuk

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Variation process: How to add a Responsible Person

Toegevoegd door: Qserve Group

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Guidance for the MHRA BREXIT | By Sue Spencer

Toegevoegd door: Pharma Wins

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Regulatory Requirements of MHRA | Regulatory Affairs | Pharmaceutics @Pharma Wins

Toegevoegd door: MHRAgovuk

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EU Exit and post-transition guidance, UK Paediatric Requirements Webinar - October 2020

Toegevoegd door: Mike Bereza

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Wholesale Dealer's Authorisation MHRA GDP Compliant Training