Pharmaceuticals

HGF has one of the largest and most experienced pharmaceutical IP teams in Europe.  Many of our patent attorneys have joined from senior positions at large pharmaceutical companies and bring extensive in-house experience of building, managing, and defending global patent portfolios to protect high-profile medicines.

Our multidisciplinary teams support clients to capture and protect innovation at all stages of drug discovery and development.  We specialise in providing early pre-filing IP strategy advice, invention capture, drafting new patent applications, patent prosecution, infringement analysis, European Patent Office (EPO) oppositions & appeals, and, in conjunction with our IP litigators, multi-jurisdictional patent litigation for patent owners and challengers. We also have specialist experience of supplementary protection certificates (SPCs), European regulatory data exclusivity, and IP due diligence to support licensing and acquisition activities. A large and growing part of our pharmaceutical practice involves contentious proceedings and many of our most experienced patent attorneys specialise in opposition and appeal proceedings before the EPO. We are regularly involved with complex, high-value multi-party oppositions, and we also work closely with our IP litigators on pharmaceutical patent disputes in national courts across Europe and at the Unified Patent Court.

Our technical expertise covers all aspects of patenting new (or repurposed) drug compounds, new physical forms of compounds (salts, solvates, polymorphs, co-crystals), pharmaceutical formulations (including advanced drug delivery platform systems), drug derivatives and conjugates (such as antibody drug conjugates and PROTACs), new manufacturing processes for making drug compounds or formulations, methods of treatment and therapeutic uses, new dosage regimens, combination therapies, personalised medicine approaches, and nutraceuticals.

Latest updates

HGF

Patent restoration

Inadvertent or accidental loss of patent rights can be distressing for patent holders and indeed for IP practitioners. The most common reason for restoration is when a patent has lapsed …

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SPCs for Combination Products – Will CJEU need to look again?

Key takeaways National courts have diverged on the interpretation of the EU Court of Justice’s latest decisions on SPCs for combination products – in particular on whether data in the …

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Event - 16th September 2026

Basel seminar - New developments in SPCs

VENUE – Der Teufelhof Basel, The Archaeological Cellar Join us on Wednesday 16th September 5:30 – 8:00 pm (CEST) for our seminar on the latest developments in Supplementary Protection Certificates …

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Playing Loose – CJEU asked to decide on combination SPCs

In a new referral (C-262/26), the EU’s Court of Justice has been asked to decide whether a medicine which receives a marketing authorisation (MA) as a monotherapy, but labelled with …

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Excipient or active ingredient? Look to the marketing authorisation…

In his recently issued (non-binding) Opinion in the Halozyme referral to the Court of Justice of the EU (C-456/24), the Advocate General has delivered a decisive “no” to the question …

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Six Sectors. Six Golds. Financial Times: Europe’s Leading Patent Law Firms 2026

HGF has once again been recognised with ‘Gold’ rankings across all six sectors in the Financial Times Special Report – Europe’s Leading Patent Law Firms 2026. We are one of …

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Pro = Active? CJEU asked to decide

In a new referral to the EU’s Court of Justice (C-794/25), the CJEU has been asked to rule on the question whether an approved pro-drug of a previously approved active …

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HGF

Santen Revisited – CJEU asked to think again on “first authorisation” for SPCs

A new referral to the Court of Justice of the EU (C-15/26) will once again consider what is meant by the “first marketing authorisation” requirement of Article 3(d) of the …

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Let's talk

If you would like to discuss how HGF could help you, contact one of our pharmaceuticals specialists.