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Practice notes
This Tracker is for use when determining whether a country is a signatory to the Hague Convention on Choice of Courts Agreements and whether the...
Produced in partnership with Cara North of Lipman Karas 10th May
Practice notes
ARCHIVED: This Practice Note has been archived and is not maintained.This Practice Note considers the rules for determining which court has...
10th May
Practice notes
This Practice Note aims to provide an understanding of what is meant by the term ‘jurisdiction’ when dealing with cross-border litigation. It explains...
10th May
Practice notes
This Practice Note explains how to review and amend key contract clauses to ensure that they are suitable for use following 11 pm on 31 December 2020,...
7th May
Practice notes
Directive 2001/83/EC (consolidated version 26.07.2019), the Pharmaceutical Code establishes a period of ‘data exclusivity’ from the initial...
Produced in partnership with Elisabethann Wright of Hogan Lovells, Fabien Roy of Hogan Lovells, Jane Summerfield of Hogan Lovells and Richard Welfare of Hogan Lovells 6th May
Practice notes
As explained in the Practice Note: Marketing authorisations in the EU—regulatory procedures for approval of medicinal products, no medicinal product...
6th May
Practice notes
In recent years, we have witnessed a constantly growing interest from all stakeholders (the general public, patients associations, physicians,...
Produced in partnership with Vincenzo Salvatore of BonelliErede 6th May
Practice notes
No medicinal product may be placed on the market without having first obtained an approval known as a marketing authorisation (MA). The MA sets out...
6th May
Practice notes
IP COMPLETION DAY: 11pm (GMT) on 31 December 2020 marks the end of the Brexit transition/implementation period entered into following the UK’s...
Produced in partnership with Geneviève Michaux, Partner, King & Spalding 6th May
Practice notes
EU and UK legal framework governing medicinal productsA complex array of requirements and guidelines developed at EU, EU Member State and UK levels...
6th May
Practice notes
On 23 June 2016, the UK held a referendum on its membership of the EU, with a majority voting in favour of the UK leaving the EU. On 29 March 2017,...
6th May
Practice notes
European level rules on pricing and reimbursement of medicinal productsThe pricing and reimbursement of medicinal products and medical devices is not...
6th May
Practice notes
IP COMPLETION DAY: 11pm (GMT) on 31 December 2020 marks the end of the Brexit transition/implementation period entered into following the UK’s...
Produced in partnership with David Knight of Fieldfisher LLP 6th May
Practice notes
This Practice Note provides an overview of the EU Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). The...
Produced in partnership with Alison Dennis and Justyna Ostrowska 6th May
Practice notes
This Practice Note explores unlicensed medicinal products and the various ways that such products may be made available to patients in the EU and UK,...
Produced in partnership with Peter Feldschreiber, 4 New Square, Lincolns’ Inn 6th May
Practice notes
IP COMPLETION DAY: 11pm (GMT) on 31 December 2020 marks the end of the Brexit transition/implementation period entered into following the UK’s...
6th May
Practice notes
ARCHIVED: This Practice Note has been archived and is no longer maintained. It contains closed legislative proposals, published judgments and closed...
6th May
Practice notes
This Practice Note discusses issues specific to patents for small molecules or ‘new chemical entities’ (NCEs), a subset of the types of material or...
Produced in partnership with Rouse Legal 6th May
Practice notes
Pharmaceutical patents (pharma patents) are a very specific part of the IP canon. They are primarily concerned with chemical compounds that are useful...
6th May
Practice notes
This Practice Note contains a jurisdiction-specific Q&A guide to pharmaceutical antitrust in France published as part of the Lexology Getting the Deal...
6th May

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