+48 881-936-710

pleng
Our plants in Poland
Valeant Pharmaceuticals International is an elite member of the international pharmaceutical industry. Polish production plants are among company's key investments, providing most of Valeant's production in Europe, while also offering top quality contract manufacturing services.
Top quality and safety of Valeant production plants are confirmed by GMP certificates and also by FDA approvals for tablets and injections. Pharmaceutical contract manufacturing services of Valeant Group Poland bring these strengths to all our customers.
Jelfa Pharmaceutical Company
Jelenia Góra
  • PRODUCT FORMS
    • injections: solutions for injections
    • solid dosage: uncoated tablets, film-coated tablets, sugar-coated tablets
    • semi-solid: dermatological products (sterile and non-sterile): ointments, creams, gels, dermatological emulsions and suspensions
    • dermatological liquids
  • PACKAGING
    • injections: ampoules, vials
    • solid dosage: blisters, bottles
    • semi-solid: aluminum and plastic tubes, bottles
  • CERTIFICATES
    • GMP, FDA
                details of certificates
  • GMP CERTIFICATE GIF-IW-N-4022/238/13 from 08.01.2014 issued by Main Pharmaceutical Inspectorate for sterile forms of medicinal products (freeze-dried products, low-volume liquids and solid-dosage forms) – valid until 10.10.2016
  • GMP CERTIFICATE GIF-IW-400/0036_01_05/04/36/14 from 30.05.2014 issued by Main Pharmaceutical Inspectorate for liquid and semi-solid forms of medicinal products including the ones manufactured in aseptic process – valid until 13.03.2017
  • GMP CERTIFICATE GIF-IW-400/0036_01_02/04/82/14 from 25.07.2014 issued by Main Pharmaceutical Inspectorate for solid-dosage forms of medicinal products (tablets, hard gelatin capsules) – valid until 08.05.2017
  • GMP CERTIFICATE GIF-IW-400/0036_01_05/04/37/14 from 30.05.2014 issued by Main Pharmaceutical Inspectorate for liquid and semi-solid investigational medicinal products - valid until 13.03.2017
  • GMP CERTIFICATE GIF-IW-400/0036_01_03/04/4/15 from 27.03.2015 issued by Main Pharmaceutical Inspectorate dla for imported human medicinal products - valid until 14.01.2018
  • GMP CERTIFICATE GIF-IW-N-4022/74/13 from 23.05.2013 issued by Main Pharmaceutical Inspectorate for quality control of human medicinal products – valid until 28.02.2016
  • U.S. Food and Drug Administration approval for sterile liquid forms and solid-dosage forms of medicinal products manufactured for US market
ICN Polfa Rzeszów
  • PRODUCT FORMS:
    • solid dosage: uncoated tablets, film-coated tablets, sugar-coated tablets, hard gelatine capsules, powders
    • liquid: syrups, drops, emulsions, suspensions
  • PACKAGING:
    • solid dosage: blisters, bottles, sachets
    • liquid: glass and plastic bottles
  • CERTIFICATES
    • GMP
         details of certificates
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-N-4022/248/13 from 25.02.2014 issued by the Main Pharmaceutical Inspectorate for liquid and semi-solid dosage forms - valid to 24.10.2016
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-400/0098_01_05/04/172/14 from 23.12.2014 issued by the Main Pharmaceutical Inspectorate for solid dosage forms valid to 10.10.2017
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-400/0098_01_04/04/28/15 from 19.05.2015, issued by the Main Pharmaceutical Inspectorate for active substances - valid to 20.02.2018
  • CERTIFICATE OF EN ISO 13485:2012, EN ISO 13485:2012/AC:2012 COMPLIANCE OF A Manufacture of medical devices in the form of gels, creams, aerosols intended for contact with skin or mucosal membranes. Distribution of non-active medical devices N° SX 600825980001 from 18.02.2013, issued by the TÜV Rheiland LGA Products GmbH for medical devices - valid to 24.01.2016
  • EC CERTIFICATE DIRECTIVE 93/42/EEC Annex V Production Quality Assurance Medical Devices N° DD 600825990001 from 18.02.2013, issued by the TÜV Rheiland LGA Products GmbH for medical devices - valid to 24.01.2018
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-N-4022/250/13 from 25.02.2014 issued by the Main Pharmaceutical Inspectorate for Importation of Human Medicinal Product - valid to 24.10.2016
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-N-4022/249/13 from 25.02.2014 issued by the Main Pharmaceutical Inspectorate for Human Investigational Medicinal Products for phase I, II, III clinical trials – Liquids for internal use - valid to 24.10.2016
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° GIF-IW-400/0098_01_05/04/173-1/14 from 23.01.2015 issued by the Main Pharmaceutical Inspectorate for Human Investigational Medicinal Products for phase I, II, III clinical trials – Tablets - valid to 10.10.2017
  • CERTIFICATE OF GOOD MANUFACTURING PRACTICES PHARMACEUTICAL AREA N° 493/2010 from 19.01.2011, issued by the Brasil Ministry of Health for Coated Tablets.
  • CERTIFICATE OF GMP COMPLIANCE OF A MANUFACTURER N° 2013-14/1 from 21.01.2013, issued by the Turkey Ministry of Health for Efudix 5% Cream.
  • CERTIFICATE GMP Clearance for semi - solid forms and liquid forms (MI-2014-CL-09376-1) issued by TGA on 12.06.2015 valid to 24.04.2017
  • CERTIFICATE GMP Clearance for solid forms (MI-2015-CL-06825-1) issued by TGA valid to 10.04.2018
Valeant Med
Warszawa
  • PRODUCT FORMS:
    • ​HEMA and PMMA intraocular lenses
    • ​capsular tension rings
  • PACKAGING:
    • universal system or preloaded injectors

 

  • The company won Polish Quality Award 2014 in middle-sized manufacturing organisations category
  • Director Marcin Dębowski won the 8th edition of Outstanding Leader Award as a part of Polish Quality Award 2014

 

  • CERTIFICATES:
         details of certificates
  • Certificate of Quality Management System EN ISO 13485:2012 for Medical Devices in the scope “Design, Manufacturing and Distribution of Sterile Ophthalmic Medical Devices and Injection Systems for Eye Surgery”.