Sanofi Vaccine - Product Scorecard

Company: Sanofi

Type: Covid-19 Vaccine
Product (brand name): VAT-00002 and VAT00008 (Vidprevtyn)
0%
compliance
with criteria
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Explore the results of PAF’s research into the behaviour of Sanofi. Each section is given an overall score; individual criteria are also scored (see icon following the criteria heading).

Click on ‘Explanation about the score’ sign next to each entry to expand and learn more.

Category A: Commitments and Accountability

The company should publicly commit to human rights in relation to product development and marketing, by adopting an official human rights policy statement recognising the right to the highest attainable standard of health. The company should endeavour to integrate human rights into its strategies, policies, programmes, projects, and activities.

The company should also have a publicly available global access plan for their Covid-19 product, based on human rights standards, with measurable targets and lines of accountability.

A1: Does Sanofi publish a global access plan for its product?

Sanofi signed the Gates Foundation ‘Commitments to Expanded Access for Covid-19 Diagnostics, Therapeutics and Vaccines’

It has also made a statement on Covid-19: “We also keep our commitment to making a strong contribution to current global public health priorities by supporting manufacturing and supply of half a billion doses of three different currently approved vaccines: BioNTech’s approved COVID-19 vaccine, co-developed with Pfizer, the vaccine developed by Johnson & Johnson, and the vaccine developed by Moderna. We are working across multiple countries and in coordination with partner manufacturing sites to make vaccines at the extremely large scales required by the pandemic. The manufacturing process is a complex, never-ending job, but our aim is to supply vaccines to as many people as possible.” 

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A2: Does Sanofi commit to comply with human rights standards in relation to product development and marketing?

Sanofi committed to the UN Guiding Principles on Business and Human Rights in 2015. It also commits to exercise due diligence to respect the fundamental rights of workers.

Sanofi also has a corporate social responsibility (CSR) statement on ‘human rights in our activities’ with examples of good practices including ‘ensuring affordable drugs and providing access to healthcare’

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Category C: International cooperation

The company should constructively engage with international initiatives for the equitable distribution of vaccines and therapeutics, such as the Covid-19 Technology Access Pool (C-TAP) or the Medicines Patent Pool (MPP), and the ACT Accelerator (COVAX). The company should also publicly commit to not enforcing the exclusive rights of Covid-19 related patents, and enter into non-exclusive, transparent licensing agreements for its Covid-19 products with other companies.

C1: Does Sanofi commit to C-TAP or MPP?

Sanofi does not commit to C-TAP or the MPP.

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C2: Does Sanofi commit to not enforcing the exclusive rights of Covid-19 related patents?

Sanofi has not made a commitment to not enforce patents.

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C3: Does Sanofi supply to, or signs agreements with, the vaccines or therapeutics pillar of the ACT Accelerator?

Sanofi signed an advance purchase agreement with COVAX for 200 million doses on the 28th of October 2020. The vaccine, however, has still not been approved.

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C4: Does Sanofi agree to license its Covid-19 medical products to other companies?

Sanofi has not entered into any licensing agreements yet.

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Category E: Equality, non-discrimination & equity

The company should engage in efforts to further equitable distribution of Covid-19 vaccines/therapeutics, by equitably distributing its supplies globally, devising fair pricing strategies, and making the active ingredient for its product available to other manufacturers. The company should also engage in full technology transfer to other manufacturers, including the necessary transfer of skills, legal components, knowledge and intellectual property. Where applicable, the company should agree to waive rights in regulatory test data, and refrain from enforcing TRIPS+ measures.

E1: Does Sanofi make the active ingredient available on reasonable grounds? [Only for therapeutics]

[Only applies to therapeutics]

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E2: Does Sanofi commit to full technology transfer to other manufacturers?

Sanofi does not commit to full technology transfer to other manufacturers (see C4).

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E3: Does Sanofi commit to non-profit, ‘fair’, or differential pricing?

Sanofi has made a commitment to affordable pricing, but nothing specific has been undertaken so far

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