Published content sits at the heart of every biotech and life science workflow

Published research, peer-reviewed articles, and industry reports inform how teams stay up to date, make decisions and communicate their work.

This published STM content underpins early discovery, development planning and the evidence behind future pipelines. But every time that content is shared, saved, reused or entered into an AI tool prompts, permission may be required.

Typical day-to-day activities include:
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Sharing journal articles with colleagues, CROs and MedComms agencies Citing studies in regulatory submissions for new drugs or clinical trials Using content in pitch decks, board reports and patent applications Prompting generative AI tools with published scientific content Storing and sharing materials between offices and partners globally

In a small founding team, this can feel manageable. As organisations scale, and as AI tools become embedded in everyday workflows, informal practices create common copyright pitfalls and become a governance gap that investors, regulators and partners increasingly look for.

AI-native workflows are accelerating content reuse

Biotech teams are among the fastest adopters of generative AI tools in the workplace, using generative tools to accelerate research, draft materials and extract insight from published studies. This often involves pasting and reusing third-party content at speed and scale, embedding copying into everyday workflows. As adoption grows, so does the volume of reuse, typically ahead of any formal AI or copyright controls.

Ad-hoc practices break down as you scale

What starts as informal, manageable behaviour in a founding team becomes harder to control as the organisation grows. Content flows across teams, partners and borders, while expectations from investors and regulators increase. Without a clear framework, content reuse becomes difficult to track, evidence and justify under scrutiny.

One licence, broad coverage, built for your industry

The CLA Pharmaceutical Licence was developed in close consultation with the pharmaceutical and life sciences sector. It gives your team consistent, lawful rights to copy and share content from millions of leading scientific, technical and medical publications.

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Support your funding journey

Demonstrate that third‑party content is being managed responsibly as part of your wider governance approach

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Scale with confidence

Replace ad hoc decisions with a consistent framework your team can rely on

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Work across borders

Enable more consistent permissions for teams and collaborators operating internationally

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Use AI responsibly

Provide a clearer basis for using published material to prompt AI tools

Choosing the right licence for your organisation

Pharmaceutical Licence

For UK-based organisations managing internal content use and regulatory compliance

Multinational Pharmaceutical Licence

For organisations headquartered outside the UK with UK operations

Extended Multinational Pharmaceutical Licence

For UK-headquartered organisations with international teams

Pharmaceutical Collaboration Licence

A free add-on that allows share among organisations that hold relevant CLA and Copyright Clearance Center (CCC) Licences

All licence variations include workplace generative AI permissions to support the reuse of opt-ed in published content in prompting permitted generative AI tools.

Not sure which licence is right for you?

Speak to our team

Supporting the way biotech teams use content

Copy, share and reuse content from a wide range of peer‑reviewed journals, books and industry sources,

Lawfully use extracts from opted-in published content to prompt permitted generative AI tools.

Support teams operating across the UK, US and more than 40 territories through licence options.

Distribute content internally and with external partners, including CROs and MedComms agencies.

One licence covers millions of publications, reducing the need for individual requests.

Ensure rightsholders and content creators are paid for their work and support the production of new STM content.

Further resources

Pharmaceutical Licence

For more information on the Pharmaceutical Licence.

Workplace AI Permissions

Maximise efficiency with CLA’s new workplace generative AI licence permissions.

Supporting the regulatory submission process

Find out why a CLA Pharmaceutical Licence is invaluable for any company developing a new drug.

Simple enquiry process

Whether you’re ready to apply for a Pharmaceutical Licence, or want to talk through the right cover for your stage of growth, fill in the form below and a member of the CLA team will be in touch.

Biotech Start-up FAQs

The same content reuse practices that established pharmaceutical organisations carry out also apply to early-stage biotech. Putting a copyright framework in place from day one supports IP governance, simplifies onboarding, and provides evidence of operational rigour during investor due diligence.
Pharmaceutical Licence fees are based on the number of professional employees, so smaller teams pay smaller fees. Contact us for a quote tailored to your headcount and international presence.
Yes. The CLA Pharmaceutical Licence includes Workplace Generative AI permissions, allowing the lawful copying and inclusion of opted-in published content to prompt permitted generative AI tools to generate outputs (subject to the terms and conditions of your licence).
While subscriptions grant access to content, there's a critical distinction between accessing content and having the rights to copy and share it. Many publications include explicit copyright statements prohibiting copying, storing or sharing, so subscriptions do not automatically grant reuse rights.
Yes, under certain conditions. You can send copies for regulatory submissions (in any jurisdiction), patent applications, or medical information requests. Sharing for external marketing is not permitted.