History

1953

ASM Aerosol-Service AG is founded in Riehen. It is the first Swiss company to produce aerosols as a contract manufacturer

1964

Start of production at the Möhlin site

1966

  • Construction of the first filling line for pharmaceutical products
  • The manufacturing license to produce medicinal products is issued to ASM for the first time

1975

Swissmedic grants manufacturing authorization for medicinal products for the first time

1980

After a period of continuous expansion, the relocation from Riehen to Möhlin is completed

1982

ASM develops and patents the Bag-on-Valve system (BOV)

1991

A new high-bay warehouse for 4,200 pallets is put into operation

1995

  • After a management buyout, ASM is privately owned
  • In the same year ASM is ISO 9001 certified

2001

Construction of a pharmaceutical filling area GMP and ISO 9001 compliant (cleanroom class D)

2003

ASM is GMP certified by Swissmedic

2005

A new pharmaceutical mixing area GMP and ISO 13485 compliant is put into operation (cleanroom class D)

2008

  • Construction of a unique multipurpose filling line (aerosol/liquid) to produce pharmaceutical and cosmetic products under GMP and cleanroom conditions (cleanroom class C)
  • ASM is ISO 13485 certified

2009

Construction of a temperature-controlled warehouse for raw materials and finished products

2012

  • ASM is ISO 22716 certified
  • Successful audit for Gulf Cooperation Council (GCC)

2013

Successful audit of the Turkish authorities Ministry of Health Turkey (MoH TR)

2014

  • A new highly flexible packaging line according to pharmaceutical standards is put into operation
  • Start with the construction of a high-bay warehouse with 3,200 storage locations according to pharmaceutical standard (explosion protection EXII and temperature controlled)
  • Participation in the energy saving program: ASM commits to reduce the legally defined energy and CO2 emissions until 2024

2015

  • An additional packaging line incl. serialization is put into operation
  • Successfully audited by FDA registration FEI-No. 3005439256
  • Finalization of the new pharmaceutical high-bay warehouse (3,200 pallet spaces)
  • Roof refurbishment of the existing chemical and finished product warehouses with the aim of further increasing energy efficiency

2016

  • Successful Pre-approval inspection by the Korean Ministry of Food and Drug Safety (MFDS)
  • Expansion of the pharmaceutical filling line with a leak detector P4
  • Implementation of a cold chain for raw materials and finished goods in the range of 2-8°

2017

  • Successful registration at the Japanese Authorities (PMDA)
  • Successfully audited by the FDA for the second time
  • Expansion of blending capacities with a development vessel 3 – 12 L, a 200 L pilot plant and a new 1800L plant, all from the same manufacturer
  • Acquisition and qualification of an additional serialization line
  • Installation of an additional Leak Detector in P3

2018

  • Decision of the Board of Directors for the long-term expansion of the site in the pharmaceutical -filling, packaging and laboratories
  • Expansion of the organization through an additional management level
  • Additional investments in new energy efficiency measures to further reduce CO2 emissions
  • Mid-year start with the introduction of a new ERP system

2019

  • Equipping all pharmaceutical packaging lines with serialization systems
  • Successful implementation of a validated ERP system
  • The 1800L mixing plant is put into operation
  • Construction of a new pharmaceutical cold store (2-8°) for approx. 100 pallets
  • Introduction of scanner systems in the warehouse
  • Successful auditing by the Ministry of Industry and Trade of Russian Federation (MITRF)

2020

  • Start of the expansion of the site by a new floor with approx. 1400 sqm of laboratory and office space
  • Another multi-purpose filling line and an additional packaging line to produce pharmaceutical and cosmetic products under GMP and clean room conditions is ordered
  • The new ex-pharmaceutical cold storage facility is put into operation
  • Introduction of a new LIMS system in the QC department
  • Russian authorities successful audit for the manufacture of additional products at ASM
  • Start the refurbishment of existing premises in P2
  • Construction of new P5 packaging and filling rooms according to pharmaceutical standards in cleanroom class C/D/E and F

2021

  • The new pharmaceutical room and the new pharmaceutical packaging plant is put into operation
  • Start of construction work for the new pharmaceutical multi-purpose filling plant (aerosol/liquid)
  • Start of construction of new ventilation and laboratory facilities
  • Modernization of the IT networks to the latest state of the art

2022

  • Finalization of the new, state-of-the-art QC and R&D laboratories, including a dedicated HIPO laboratory with separate personnel and material locks class H14
  • Move into the new office premises
  • Expansion of the parking lots and the surrounding area
  • Commissioning of an additional transformer station
  • The new pharmaceutical multi-purpose filling line P5 is put into operation
  • Implementation of the first PV systems to generate electricity for own use
  • Various digitalization projects launched and implemented (HR, QA, QC)
  • Defined reduction of energy and CO2 emissions target already achieved or exceeded

2023

  • Installation of another PV system
  • Start renovation of the last production premises

 

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