Laboratoire Aguettant


Aguettant is a family-owned pharmaceutical laboratory based in Lyon, France, dedicated to developing, manufacturing, and marketing injectable pharmaceutical specialties used in hospitals. With over a century of experience, it focuses on innovative injectable medicines, especially in emergency, anesthesia, neurology, and parenteral nutrition. The company emphasizes research and development, quality, and international expansion, holding numerous approvals and certifications. It is committed to ethics, transparency, and sustainable development, actively engaging in RSE practices and social responsibility.

Industries

manufacturing
pharmaceutical

Nr. of Employees

large (251-1000)

Laboratoire Aguettant


Patents

Medical device including a package and a pre-filled syringe disposed in the package

US-11052186-B2

View Details

Injection assembly

US-9675763-B2

View Details

Pre-filled hypodermic syringe fitted with a stoppering device

US-8118788-B2

View Details

Products

Prefilled syringes (sterile injectables)

Sterile prefilled syringe formats for hospital and clinical use.

Glass vials and ampoules (injectable solutions)

Aseptic or terminally sterilized injectable products in glass vials and ampoules.

Plastic containers and blow-fill-seal products

Plastic containers manufactured via blow‑fill‑seal and extrusion processes, including bottles, irrigation solutions and multi‑liter containers.

Injection pens and assembled devices

Manufacture and assembly capability for injection pens and associated packaged systems.

Hospital-use therapeutic product categories

Portfolio covering emergency medicine and resuscitation, anesthesia, neurology (including Parkinson's treatment), parenteral nutrition components and irrigation solutions.


Services

GMP manufacturing and filling of sterile injectable products across multiple container formats (syringes, vials, ampoules, bags, bottles) with aseptic and terminal sterilization options.

Physico‑chemical, microbiological and functional laboratory testing for release, stability and regulatory compliance.

Formulation development, evaluation of ideas, development of administration systems, method development and preparation of documentation for regulatory submissions.

Preparation and compilation of technical and regulatory documentation for marketing authorizations and medical device conformity (CE) processes.

Safety monitoring, case collection, analysis and reporting of adverse events to authorities; staff training on pharmacovigilance processes.

Storage, preparation and global shipping of finished pharmaceutical products from a dedicated logistics platform; incoming materials reception and sampling.

Expertise Areas

  • Injectable drug development
  • Aseptic and terminally sterilized sterile manufacturing
  • Blow-fill-seal container manufacturing
  • Analytical method development and QC testing
  • Show More (6)

Key Technologies

  • Blow-fill-seal (BFS)
  • Aseptic filling
  • Terminal sterilization
  • Prefilled syringe manufacturing
  • Show More (6)

Similar organizations

Browse all ORGANIZATIONS

JOIN OUR MAILING LIST

Stay Connected with MTEC

Keep up with active and upcoming solicitations, MTEC news and other valuable information.