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Special Report                                                                 Special Report



 Tariffs, strategies & biotech: Where do things   need  at  least  12  months  to  fi nd  alter-  grow  global resilience and position-  Establish a Biotech for Europe Initiative
       native suppliers, and 44% said it would  ing. We have called on the [European]  to support the acceleration  of R&D
 stand?  require more than two years.    Commission to accelerate the positive  and development of biotech  and bio-
                                         work  already underway for biotech  manufacturing through direct fi nancing
 iotech industry groups, Biotech-  Another set of tariffs, separate and   PATRICIA VAN ARNUM  “This survey demonstrates the  through the Biotech Communication  (loans and grants) for development and/
 nology Innovation Organization  specifi c  to  the  pharmaceutical  indus-  Editorial Director, (DCAT)  far reaching and potentially  damag-  of 2024, with regulatory streamlining,  or scale-up programs in the EU.
 B(US) and EuropaBio (Europe),  try, are also under evaluation. In April   ing impacts of the proposed tariffs on  and the EU Biotech Act. This ambition
 weigh in on evolving US  trade policy  2025, the US Department of Commerce   Throughout this process,  the bio-  our biotechnology industry, on biome-  should also be translated  into related   Improve  EU  fi nancial  and  capital
 and how to strengthen the life-sciences  initiated an investigation to determine  technology industry, via BIO and   dical research and  on patients,” said  initiatives  including the Life Sciences  markets for innovation. Take  forward
 industry’s competitiveness.  the effects on US national security of  EuropaBio,  which represent  both large   BIO President and CEO, John F. Crow-  Strategy, Pharma Package, and Bio-  the measures announced in the Euro-
 imports of pharmaceuticals and pharma-  and small biotechnology  and bio/  ley, in a March 26, 2025, statement.  economy Strategy, to secure EU leader-  pean Commission’s Communication
 Weighing in on tariffs  ceutical  ingredients. The  investigation  pharmaceutical companies, have com-  “We fully support strong policies and  ship across value chains and industrial  on  a  Savings  and  Investment  Union
 How tariffs will evolve in the US is  was  initiated  under Section 232 of  mented on the potential harmful impact   programs that incentivize  the manu-  ecosystems.”  (an initiative  to improve the way the
 very much a situation in fl ux, but two  the  Trade Expansion Act of 1962, as  that tariffs would have on the industry.   facture of medicines here in America.   EU  fi nancial  system  channels  savings
 industry associations  representing  the  amended, which allows the President to  On March 26, 2025, BIO released the   Re-onshoring key parts of the biotech-  EU’s Life Sciences Strategy  to productive investments) to improve
 biotechnology industry, the Biotechno-  impose import restrictions based on an  results of a survey of its members taken   nology supply chain to the US and our   The European Commission is  pre-  the competitiveness of EU fi nancial and
 logy Innovation Organization (BIO) in  investigation  and  affi rmative  determi-  in February 2025 that underscored the   allies and strengthening the American  paring a new Strategy for European  capital markets for  innovation-driven
 the US and EuropaBio in Europe, have  nation by the US Department of Com-  global nature of the bio/pharmaceutical   manufacturing  base should be a high  Life Sciences, to be adopted  in 2025,  industries.
 both issued statements  over the nega-  merce that certain imports threaten to  supply chain  and the  negative  impact   priority for both national and economic  as a means to strengthen life-sciences
 tive impact that tariffs could have. As  impair US national security. In general,  that tariffs would have, particularly on   security. It will take years, though, for  research and innovation in the EU and   Patent reform. Accelerate  the  roll-
 of April 24, 2025, the US government  a Section 232 investigation  considers  imports from the European Union (EU).   this shift, and we need to be mindful of  invited public comment on the strategy,  out of the Unified Patent System,
 has imposed a  baseline  tariff of 10%  the following (1) existing domestic  Globally, according to the study, nearly   the negative consequences of these pro-  which ended on April 17,  2025. Both  including creating a one-stop shop for
 on all US imports and two additional  production of the product; (2) future capa-  90% of US biotech companies rely on   posed tariffs.”  EuropaBio and the European  Federa-  patent protection  and enforcement
 sets of tariffs are under consideration:  city needs; (3) manpower, raw mate-  imported components for  at least half   tion  of Pharmaceutical  Industries and  across the EU, and encourage all EU
 (1) reciprocal taxes, which are imposed  rials, production equipment, facilities,  of their FDA-approved products. With   EuropaBio, which represents bio-  Associations (EFPIA), which repre-  member states to ratify and implement
 on a country-by-country basis; and (2)  and other supplies needed to meet pro-  respect to the EU specifi cally, the study   tech  and  bio/pharmaceutical compa-  sents innovator drug companies and  the agreement.
 specifi c pharmaceutical industry tariffs.  jected national defence requirements;  found  that  94%  of  biotech  fi rms  anti-  nies in Europe, weighed in on the tariff  national pharmaceutical association in
 (4) growth requirements, including the  cipate higher  manufacturing costs  if   situation on  April 8, 2024, prior to the  Europe, issued  recommendations  for   EU R&D funding support. Support
 The  Trump  Administration  fi rst  investment,  exploration, and develop-  tariffs are placed on imports from the   90-day pause on reciprocal  taxes and  the European Life Sciences Strategy to  life sciences innovation by preserving
 laid out a plan for imposing reciprocal  ment to meet them; and (5) any other  EU and that  proposed tariffs on the   the later action of the US government  be considered by EU policymakers.  “Framework Program 10” funding
 tariffs in February 2025 as a means to  relevant  factors. For pharmaceuticals,  EU would oblige 50% of companies to   to initiate an evaluation of specifi c tariffs   levels (the  EU’s funding plan to
 counter non-reciprocal trading arrange-  the US Commerce Department provided  potentially fi nd new research and manu-  on the pharmaceutical industry. It  EuropaBio’s recommendations  support, research, science and innovation)
 ments with its trading partners and as  public  notice  in the Federal Register  facturing partners. In addition, overall,   called  for an exemption  of tariffs on   A key point made by EuropaBio is  and continue to support public-private
 a way to improve US competitiveness,  of its Section  232 investigation  into  half of  those companies surveyed say   bio/pharmaceuticals and a continuation  that EU policy needs to better support  partnerships.
 including in manufacturing. Those reci-  pharmaceuticals on April 16, 2025, and  they would have to rework or poten-  by EU policymakers to advance the  product  innovation  and the  transla-
 procal taxes were scheduled to go into  is requesting public comment by  tially delay regulatory fi lings, and 80%   competitiveness  of the EU biotechno-  tion of research into commercial pro-  University funding support. Accele-
 effect on April 9, 2025, but the Adminis-  May 7, 2025.  of biotech companies said they would   logy industry through several strategic  ducts through greater  public  spending  rate academic  discovery into industry
 tration  placed  a 90-day pause (until   policy and legislative proposals.  in  R&D,  incentives  for  fi nancial  and  by earmarking  additional  EU funding
 July 9, 2025) on their implementation   capital markets as  well as  regulatory  for universities with high-tech  trans-
 to enable countries to negotiate these   “In this critical moment, EuropaBio  reforms. With respect to fi nancial and  fers/spin-offs and establish metrics to
 tariffs  with the US  government. One   actively supports  the European Com-  capital  markets, EuropaBio  is recom-  measure impact of discovery of trans-
 exception was China, which had issued   mission, our company members and  mending the following:  lational research and incentivize higher
 trade  countermeasures in response to   national biotech  associations to  en-  technology readiness levels.
 the pending reciprocal tariffs imposed   hance EU  ambition, competitiveness   Biotech and  Life  Science Index.
 on it. It is now subject to a 125% import   and attractiveness  for biotech innova-  Establish a Biotech and Life Science   On the regulatory front, EuropaBio
 tariff announced by the White House on   tors of all sizes,” said EuropaBio, in an  Index allowing biotech companies to  is recommending the following:
 April 9, 2025, plus an additional 20%   April 8, 2025, statement. “Specifi cally,  raise capital, including in later stage
 fentanyl-related tariff already imposed   EuropaBio  calls for an  exemption  for  where signifi cant gaps exist, from EU   AI and digital transformation.
 in February and March (2025), effec-  biopharmaceuticals  and their  manu-  investors in high liquidity markets.  Accelerate the digital transformation,
 tively creating a 145% tariff rate on   facturing inputs, plus  strengthening   including the use of AI, in priority areas
 imports to the US from China.  biotech  value  chains, to  preserve  and   Biotech  for Europe Initiative.  such as green processes, product ap-

 170  Chemical Weekly  May 13, 2025  Chemical Weekly  May 13, 2025                                     171


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