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Helping pharma thrive

Testing excellence for speed to market

Innovation in pharma offers huge potential for improving human life. Research labs are at the forefront of these developments. By helping to automate testing protocols and day-to-day data collection, Clinisys™ enables labs to focus their energy on solving sophisticated science challenges in pharma while improving their developmental speed and ensuring they can reach market as quickly as possible.

Reducing complexity to deliver results

The deep experience we have in serving pharma labs allows us to help relieve challenges faced by industry. Our goal is to help accelerate innovation, improve team productivity and motivation, and ensure that your lab maintains quality and compliance with strict industry regulations. We help pharma labs meet these goals so they can bring their solutions to market to improve lives everywhere.

CLS industry content packages

Advance pharma testing

Clinisys enables pharma labs to research and test more efficiently, reducing the complexity of new drug development, ensuring efficacy, and generating wide impact promised by health innovations and genetic medicines.
Scientist Working in The Laboratory
Scientist Working in The Laboratory

Reduce pharma time to market

Quick innovation is needed to develop pharmaceuticals and bring lifesaving new drugs and genetic medicines to market. Clinisys supports the effective exploration of potential new products by enabling labs to safely conduct new drug research and development. We help your team operate efficiently, keep stakeholders informed, disseminate research milestones, and gather test data that will smooth your operations.

Innovate freely

Pharma labs face pressure to innovate quickly to create drugs that are effective and relevant to market needs. In the face of those challenges, labs need a partner like Clinisys to help them organise their operations and systems to deliver quickly and safely. We help you collect data and collaborate with clients and partners in near real-time for rapid and free innovation.

Improve morale and productivity

Our pre-configured workflows and processes ensure sophisticated testing protocols are followed. Routine testing can now be highly automated, using instrument data capture wherever possible. We help your team of research scientists and lab professionals focus on more complex and rewarding problem-solving tasks.

Maintain compliance, satisfy regulators

Pharma is a highly regulated sector. Our proven workflow means your protocols are followed during research, design, and trial stages. Using comprehensive test data gathered throughout every stage, our lab solutions help you to satisfy the FDA 21 CFR Part 211 requirements for auditing and compliance efficiently. Our global presence ensures our solutions help you meet national and international standards.

Answering your frequently asked questions

Our pharma solutions take advantage of the highly scalable, cloud-based Clinisys platform. It seamlessly accommodates rapid growth in volumes and the need to add new services or locations.

Our solutions reduce regulatory burden. We automate data collection where possible throughout the lifecycle to eliminate human error. We provide a full audit trail of data to achieve client reporting, offer service-level performance, and support complex regulatory reporting.

For a full list of the regulations relevant to your specialisation, please get in touch.

We support laboratories of all types and sizes, both in-house and outsourced contract services labs. These range from smaller labs specialising in a single industry or scientific discipline to large multidisciplinary organizations serving their clients across many industries and services. Our locations around the world enable us to support both local and multinational organizations.

Clinisys solutions are highly configurable. We have proven workflows available to accelerate your deployment. We also enable the rapid creation of unique workflows to support your lab’s own processes and methodologies, or to serve your research programme’s requirements.