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Printed By


David Wallace

Executive Editor

Birmingham, UK

Having previously worked in the European chemicals industry, Dave has been with Generics Bulletin since 2010. Keeping a close eye on deals, corporate strategy and market developments in the off-patent sector, he also brings his background and education in law to bear on industry litigation as well as national legislative and regulatory affairs, with a particular interest in France where he has lived and studied in the past. A regular delegate to generics and biosimilars events and conferences as well as a frequent panel moderator, he maintains close links with industry representatives around the world. He also organizes and judges the annual Global Generics & Biosimilars Awards. In his spare time, he enjoys art and playing the piano.

Latest From David Wallace

One Month Remains To Enter 2024 GGB Awards

Just one month remains for companies to submit their entries to the Global Generics & Biosimilars Awards 2024, ahead of our ceremony in October.

Generic Drugs Biosimilars

‘A True Seat At The Table’ – Irish Industry Leader Sets Out Aspirations For New Pricing Deal

With a fresh pricing deal on the horizon, Medicines for Ireland chair and Teva country head Paul Neill talks to Generics Bulletin about the need for the Irish off-patent industry to have “a true seat at the table” and secure an agreement with the country’s government that better reflects the specificities of the generics and biosimilars market.

Ireland Generic Drugs

‘We Tried It, It Does Not Work’ – The Problems With The EU’s SPC Manufacturing Waiver

While the European supplementary protection certificate manufacturing waiver was once seen as a triumph for the region’s off-patent industry, concerns are now being raised over how the mechanism is implemented. Attendees at Medicines for Europe’s legal affairs conference in Dublin last week heard the latest.

Europe Legislation

Biosimilars: US FDA Heralds The End Of Switching Studies For Interchangeability

New guidance suggests that switching studies will no longer be expected as standard to support determinations of biosimilar interchangeability; instead, analytical and clinical data may suffice.

Biosimilars Guidance Documents

FDA Heralds The End Of Switching Studies For Biosimilar Interchangeability

New guidance published by the US FDA suggests that switching studies will no longer be expected as standard to support determinations of biosimilar interchangeability, with the agency instead suggesting that analytical and clinical data will suffice.

Guidance Documents Biosimilars

Rosemont Takes First Steps Outside UK With Acquisition In Greece

Having earlier this year outlined plans for international expansion, liquids specialist Rosemont has made its first venture outside the UK by acquiring Greek R&D organization Pharma-Data.

Deals M & A
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