La Force in
Life Sciences
agap2, a strategic partner to the life sciences sector throughout the life cycle of healthcare products
Therapeutic innovation is picking up speed, regulatory requirements are becoming stricter and societal expectations are changing. Against this background, stakeholders in the sector need to move forward quickly, without compromising on the quality, compliance or safety of their projects. In a market under pressure, we also need to be able to recruit, train and mobilise the right profiles at the right time.
In a sector undergoing major change marked by digitalisation, regulatory pressure, health sovereignty issues and growing expectations in terms of sustainability, our mission is clear: support stakeholders in the life sciences sector to ensure the success of their strategic, technological and operational transformations, providing them with targeted expertise and concrete solutions.
For over 15 years, agap2 Life Sciences has been supporting stakeholders in the sector throughout the entire life cycle of healthcare products. Our teams mobilise their scientific, industrial and regulatory expertise to transform innovations into reliable, compliant, high-performance solutions.
Our ambition is to safeguard every stage of a project, guarantee audit-ready implementation and optimise time-to-market thanks to our agile teams working close to the field.
We design and ensure the reliability of your processes, equipment and infrastructure, from development to production.
We ensure your projects comply with the regulations, we reduce risks and guarantee document control.
We speed up the validation phases and ensure successful commissioning to meet market launch deadlines.
We support your complex projects from a technical, contractual and operational point of view, while guaranteeing overall consistency, compliance with requirements and adherence to the cost-quality-deadline triangle.
We can provide support for all or part of the life cycle of a healthcare product, from the laboratory to market launch.
Taking into account the authorities’ regulatory requirements from the earliest stages to guarantee compliant, audit-ready projects.
Teams close to operations with in-depth knowledge of the business and production environments, to ensure smooth communication, reduce lead times and guarantee that the key stages of the project are successfully completed in the correct sequence.
Control of critical milestones to reduce lead times and make project execution more reliable.
Expert profiles, selected based on the issues at stake and supported by ongoing skills development for our teams.
expertise in life sciences
in project management
mobilised for high-stakes projects.
Each assignment carried out by agap2 has a twofold objective: operational success and the real usefulness of the project. We believe that engineering is not there to do 'more' but to do better, to create value where it counts.
What you expect from a partner is that they understand your industry before you even get started.
That is exactly what we found with agap2 Life Sciences.
Are you considering working with agap2 on a life sciences project?
Here are the answers to the most common questions our customers ask before launching an assignment.
We explain everything, from life cycles, standards and commitments to profiles and confidentiality.
Does agap2 work on projects in the field of drugs, medical devices and cosmetics?
Yes. Our teams work on projects in all areas of the healthcare industry from pharmaceuticals and biotech to medical devices, fine chemicals, cosmetics and food.
Are your consultants trained in the regulatory standards (GMP, BPF, ISO 13485, etc.)?
Yes. Our employees are trained in the sector's quality and regulatory requirements, and are supported by our technical leads according to the type of project.
Can agap2 work on a project in the R&D phase or only in production?
We work across the entire life cycle: R&D, industrial transfer, qualification/validation, production, maintenance, compliance or audits.
Do you offer support with quality and documentation or just technical support?
Both of them. We have expertise in quality assurance, validation, compliance and technical documentation, as well as in processes, equipment and digitalisation.
Do you work on sites subject to multiple regulations or international sites?
Yes. Our teams can work on multi-site projects, with FDA, EMA or ANSM requirements, both in France and internationally.
