GxP Quality Assurance, Compliance and Technology services for life-science companies
Founded in 2022 as a joint venture between two established consulting firms, Epiqure brings together a broad and integrated portfolio of services across the GxP spectrum.
50+
Clients
Worldwide
120+
EXPERTS
across 10+ countries
150+
PROJECTS
DELIVERED
3
YEARS
OF GROWTH
Inspired by Philosophy, defined by Purpose
The name Epiqure takes its roots from Epicurus (Greek: Ἐπίκουρος / Epíkouros), meaning helper, ally, assister. This reflects our core identity and purpose — being a true partner to our clients.
Quality at the Core
We replaced the “C” in Epicure with a “Q” — a deliberate choice that emphasizes our unwavering commitment to Quality. It’s what drives us, defines us, and guides how we empower life-science companies every day.
A Logo that tells a Story
Our logo features two intertwined rings forming a chain — a symbol of partnership and mutual support. It represents both our origin, born from the merger of two partner companies, and our ongoing mission:
To be our clients’ Quality Allies, supporting their most critical Quality and Technology challenges.
Dedication
We listen, assess, acknowledge your business requirements
Tailor-made approach
We offer solutions designed and conceived for you
Competence
We leverage on our know-how to deliver high quality services
Agility
We operate with flexibility and reactiveness to meet your expectations
Tailored Expertise. Global Talent. Unified Vision.
At Epiqure, we believe that exceptional consulting starts with selecting the right people for the right project—every time. That’s why we’ve developed a flexible, hybrid delivery model that combines the stability of an internal core team with the reach and specialization of a global network of GxP professionals.
Whether the need is strategic or operational, local or cross-border, our model allows us to carefully match each assignment with highly qualified consultants—chosen for their technical depth, regulatory knowledge and proven field experience.
The Areas of our Expertise
Manufacturing and Distribution
We support compliance in manufacturing and distribution operations, ensuring regulatory alignment, quality oversight and supply chain integrity.
Clinical Research & Pharmacovigilance
We provide expertise in clinical development and drug safety, supporting systems, audits, inspections, and risk management throughout the pre-clinical, clinical and post-marketing phases.
Technology & Digital Compliance
We design, assess, and optimize GxP-critical systems, ensuring technology supports business goals while meeting regulatory expectations—across eTMF, PV systems, validation, data integrity, and more.
Each engagement is guided by leaders who bring decades of hands-on experience, supported by a delivery team committed to quality and adaptability. This allows us to scale precisely to client needs, offering senior-level consulting support that is both reliable and responsive—no matter the challenge.
The following section introduces the experts behind Epiqure’s success: our founders and Business Unit leaders, our internal consulting team, and the seasoned industry professionals who make up our extended network.
Giovanni Curotto
President of Epiqure AG &
Head of GMP/GDP Business Unit
A certified Qualified Person with more than 30 years of experience in pharmaceutical Manufacturing and Distribution, from Quality Culture to Inspection and Audit Management.
Roberto Molettieri
President of Epiqure France & Head of GCP, GVP & Tech Business Unit
Pharm D., M.Sc. with more than 18 years of experience in PV, Drug Safety, Clinical Research, Project Management, GxP electronic systems, Quality and Compliance.
Internal Team
Strategic Coordination, Reliable Execution
Our internal team of 8 experienced professionals ensures seamless execution, from project coordination to service delivery, maintaining the highest standards of quality.
Industry Expert Network
Decades of Global Regulatory Experience
Our extended team includes Subject Matter Experts, former Quality Directors, Auditors, and Health Authority Inspectors (FDA, MHRA), each bringing 10–35 years of hands-on industry experience.