The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK’s stand-alone medicines and medical devices regulator, taking any decisions and carrying out any functions which were taken or carried…
The Human Medicines Regulations 2012, as inserted by the Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (HMRs) contain provisions to ensure that where appropriate, medicines are adequately studied in…
OverviewTo be registered as a broker by the Medicines and Healthcare Products Regulatory Agency (MHRA), you must comply with good distribution practice (GDP) and pass regular GDP inspections of your…
Article 20(2) of Directive 2014/40/EU [TPD] places an obligation on the manufacturers and importers of electronic cigarettes to submit a notification to the competent authorities of the Member State of…
Submission of notifications for Northern Ireland under article 20 of directive 2014/40/EU.Article 20 of Directive 2014/40/EU [TPD] places obligations on the manufacturers and importers of electronic cigarettes including the requirement…
