For 18 years, pi Life Sciences has been a global integrator of excellence for the world’s leading life sciences companies. We create value for our clients worldwide by relying on the expertise of our engineers.
Dedicated exclusively to the life sciences sector, pi differentiates itself through services adapted to the specific needs of our partners and a thorough knowledge of industries such as (bio)pharmaceutical, biotechnology, medical devices and advanced therapy medicinal products (ATMPs).
At pi Life Sciences, we focus on two key action areas to support you from start to finish and ensure the complete success of your projects.
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We employ highly qualified consultants in all the ATMP production life cycle dimensions. Our experts can work with you to build or upgrade your manufacturing and product control strategy.
Biotechnology and Pharmaceutical
We support these biotech companies in this crucial challenge. As a specialist with solid experience in life sciences consulting, we provide the best consultants with a vision to optimize our partner’s processes.
At pi Life Sciences, we have the expertise to help medical device manufacturers and distributors meet the market’s regulatory requirements throughout a medical device’s entire life cycle.
Our mission is to assist you with the qualification of process equipment and laboratory instruments or with the validation of processes and laboratory methods. Given the current digitalisation efforts in our sector, we help you transition from a traditional computerised validation approach towards a computer system assurance strategy.
pi helps you create and implement a lean and risk based quality system encompassing all necessary elements for production, quality control, materials management, facilities and equipment, packaging and labelling leading to a quality manual ready to withstand regulatory audits and supporting patient safety
Our automation engineers are specialists and will improve the productivity and performance of your production lines by implementing intelligent systems controlling your process.
We have an in-depth understanding of local and overseas regulations and standards applicable to the manufacture of medicines and medical devices. We can support our partners in accelerating product development while remaining committed to quality.
As a pharmaceutical company, always in a process improvement mindset, you must remain compliant with strict rules and guarantee the safety of your products towards the patient. Our Regulatory Affairs experts ensure that your company complies with all the rules and requirements of the evolving market.
Our CSV consultants bring extensive design, project management, application, and technical experience to every computerized system assignment. We can help you assess your challenges and define the best strategies for remediation of existing systems and implementation of new systems.
Project management is essential when a team is implementing a new project. Our Project Managers are responsible for the accomplishment of each project’s objectives and are the leaders and main point of communication for all stakeholders through its different phases.
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