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The more you spend, the more you get? The effects of R&D and capital expenditures on the patenting activities of biotechnology firms

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Abstract

This paper provides evidence on the mechanisms influencing the patent output of a sample of small and large, entrepreneurial and established biotechnology firms from the input of indirect knowledge acquired from capital expenditures and direct knowledge from in-house R&D. Statistical models of counts are used to analyse the relationship between patent applications and R&D investment and capital expenditures. It focuses on biotechnology in the period 2002–2007 and is based on a unique data set drawn from various sources including the EU Industrial R&D Investment Scoreboard, the European Patent Office (EPO), the US Patent and Trademark Office, and the World Intellectual Property Organisation. The statistical models employed in the paper are Poisson distribution generalisations with the actual distribution of patent counts fitting the negative binomial distribution and gamma distribution very well. Findings support the idea that capital expenditures—taken as equivalent to technical change embodied in new machinery and capital equipment—may also play a crucial role in the development of new patentable items from scientific companies. For EPO patents, this role appears even more important than that played by R&D investment. The overall picture emerging from our analysis of the determinants of patenting in biotechnology is that the innovation process involves a well balanced combination of inputs from both R&D and new machinery and capital equipment.

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Notes

  1. The first two releases of the Scoreboard, in 2004 and 2005 dealt with the top 500 and top 700 EU and the top 500 and top 700 non-EU companies, respectively.

  2. Matching patent datasets with a list of company names, or playing the “names game” as aptly called by Melamed (2006), is a preliminary and controversial step in the assessment of organisations’ patent portfolios. Nevertheless, given the relatively small number of cases, we maintain that the potential problem of reliability has been substantially alleviated by our manual procedure. Since addressing this issue is beyond the scope of our paper, we refer to Melamed (2006), Thoma (2007), Raffo and Lhuillery (2009), and Thursby et al. (2009) among others for more in-depth discussion and proposals for alternative procedures.

  3. Being aware of the advantages and disadvantages of the use of patent-based innovation output indicators (Santarelli and Piergiovanni 1996), in this study we rely upon the assumption of homogeneity of technological content and economic significance of patents within the same technological field. Heterogeneity is conversely assumed to arise from the choice of one or multiple patent institutions.

  4. It has to be considered that both the EPO and USPTO publish all patent applications 18 months after their filing date. However, the USPTO does not publish applications which have been withdrawn or filed with a non-publication request, stating that the application is US only.

  5. Because the US is the world's leading country for the commercial development of biotechnology, companies have a strong incentive to apply for patent protection with the USPTO.

  6. Another important source, the Japanese Patent Office (JPO), has also been excluded. With the JPO, each claim beyond the first requires additional official fees for substantive examination and maintenance. As a consequence of the additional fees, Japanese patents tend to average fewer claims than EPO and USPTO patents. As a result, this system has been seen to encourage numerous filings of narrow claims that build incrementally on fundamental technologies developed by domestic and foreign inventors (Maskus and McDaniel 1999). Thus, for the sake of procedural homogeneity, we decided not to use patent applications with JPO.

  7. According to a detailed report on biotechnology in eighteen European countries and the US (Critical I, 2006), at the end of 2004 the total number of companies in business was 4,154. Thus, the representativeness of our sample with respect to the population of biotech firms in such countries is below 3.0%.

  8. According to OECD (2009), DBFs are firms whose predominant activity involves the application of biotechnology techniques to produce goods or services and/or to perform biotechnology R&D.

  9. In such a case, it is of course unlikely that DBFs invest heavily in new machinery and capital equipment.

  10. This explains the minimum values of zero found for capital expenditure between 2002 and 2006.

  11. Nevertheless, it has to be noticed that the number of patent applications is increasing over time. These figures may also reflect the fact that the monetary figures provided by the Scoreboard are not deflated, but simply converted in €.

  12. It is worth recalling that the regression cannot be linear with count variables. The problem of nonlinearity is handled through nonlinear functions that transform the expected value of the count variable into a linear function, of the explanatory variables. Such transformations are referred to as link functions.

  13. For the purposes of the Scoreboard, companies are allocated to the country of their registered office, which sometimes can be different from their operational or R&D headquarters. The main implication is that company location is independent of the actual location of its R&D activity. Use of this dummy variable is particularly important to take into account the fact that, in the US and other countries, it is common practice to include engineering costs relating to product innovation in R&D expenditures. These engineering costs have been excluded from the Scoreboard only if they have been disclosed separately. Accordingly, an overstatement of some overseas R&D investment figures in comparison with the EU is possible.

  14. Defined, consistent with the OECD “Frascati” Manual (“Guidelines for the collection of R&D data”), as the cash investment funded by the companies themselves.

  15. Defined as “expenditure used by a company to acquire or upgrade physical assets such as equipment, property, industrial buildings.”.

  16. Defined as the total number of consolidated average employees, or year-end employees if average not stated.

  17. As in fact is the case with each of the three patent counts.

  18. For the population of Italian DBFs, Santarelli and Lotti (2008) found a strong positive and statistically significant relationship between patents with EPO and profitability.

  19. Even though they use a stock measure such as capital intensity, i.e. the capital-labour ratio.

  20. Possibly trying to avoid the drawbacks consequent upon the creation of CAFC in the United States. See Section Data and summary statistics above.

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Correspondence to Enrico Santarelli.

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Previous versions of this paper have been presented at CONCORD 2010—Conference on Corporate R&D (Seville, 3–4 March 2010), at the Workshop on “The Output of R&D Activities: Harnessing the Power of Patents Data-II” (Seville, 27–28 May 2010), and at the 37th Annual E.A.R.I.E. Conference (Istanbul, 2–4 September 2010). The work has benefited from the comments by Michele Cincera, Vincenzo Spiezia, Alessandro Sterlacchini, Marco Vivarelli, and an anonymous reviewer. The views expressed are purely those of the authors and may not in any circumstances be regarded as stating an official position of the European Commission and of Istat.

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Appendix

See Table 7.

Table 7 Correlation matrix

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Piergiovanni, R., Santarelli, E. The more you spend, the more you get? The effects of R&D and capital expenditures on the patenting activities of biotechnology firms. Scientometrics 94, 497–521 (2013). https://doi.org/10.1007/s11192-012-0711-z

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