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Register to vote Register by 18 June to vote in the General Election on 4 July.
This report makes recommendations on whether to regulate practitioners of herbal medicine and the products they use to keep the public safe.
A list of herbal ingredients which are banned or restricted for unlicensed medicines.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The committee advises on the safety and quality of herbal medicines when there's an application for registration, marketing authorisation or product licence.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Advisory Board on the Registration of Homeopathic Products and Herbal Medicines Advisory Committee Annual Reports 2016, along with a record of members' interests in the pharmaceutical industry.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. CHM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care .
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
The MHRA is undertaking a public consultation on proposals to end the 'sell through' of unlicensed herbal remedies legally on market at April 2011.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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