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European Pharma R&D (RSFF)

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European Pharma R&D (RSFF)

  •  Reference: 20080550
  •  Release date: 19 November 2008
Promoter – Financial Intermediary

The promoter is one of the top 20 pharmaceutical companies in the world and the largest generic pharmaceutical company.

Location
  • Netherlands
  • Israel
  • Hungary
  • United Kingdom
Description

The project concerns the promoter’s R&D for new generics and biosimilars. It includes investments in research, development, clinical trials and regulatory approval.

Objectives

The project will contribute to private sector investments in R&D, located in Hungary, the Netherlands, the UK and Israel, thus meeting the orientations that underpin the Lisbon’s Council decision and the Bank’s Knowledge Economy (i2i) Initiative. The promoter’s collaboration with smaller companies, in particular in the biotechnology industry, adds to the diffusion and transfer of knowledge across Europe; the partnering with companies and Contract Research organisations (CROs) helps to translate knowledge into new products. Thus, EIB financing of the R&D development costs corresponds with the Community’s role to encourage Research and Technological Development, as defined in Article 163 of the EC Treaty and with the “Common Interest” criterion retained for the Treaty’s Article 267 point (c), i.e. the Bank’s financing activities under the Knowledge Economy (i2i) Initiative: (i) research & development and (ii) innovation. In addition, the project is eligible under the Risk Sharing Finance Facility (RSFF).

As a substantial part of the project is located in a convergence area in Hungary, the project is also partly eligible under the Treaty’s article 267 point (a) convergence. The part of the project that is located in Israel is eligible under the Bank’s mandate for the country.

Comments
 
Sector(s)
  • Industry
Proposed EIB finance (Approximate amount)

EUR 200 million.

Total cost (Approximate amount)

EUR 426.84 million.

Environmental aspects

The R&D activities encompassed within this project will not materially change current R&D practices and will be carried out within existing facilities, mostly in the EU and Israel, making use of existing laboratories, pilot plants, clinical centres etc. Thus an EIA according to the EU Directive 97/11 as amended by Directive 2003/35 or according to the local legislation in a non-EU country is not required. Compliance of R&D activities with relevant EU legislation will also be verified during appraisal.

Procurement

The Promoter is a private company not operating in the Utilities sector, and is thus not covered by EU Directives on procurement. Procedures followed will be verified during appraisal.

Status

Signed   -   22/12/2008.


Disclaimer

Before financing approval by the Board of Directors, and before loan signature, projects are under appraisal and negotiation. Therefore data provided on this page is indicative and cannot be considered to represent official EIB Policy (see also the Explanatory notes).



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