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The Biocidal Products Regulation or BPR (Regulation (EU) No. 528/2012) is a constantly evolving legislation with numerous implementing and delegated acts and Commission decisions published since the BPR entered into force on 1st September 2013.
LKC supports your successful product authorisations:
  • Expert regulatory advice to develop the innovative strategies and cost-effective route to authorisation;
  • Technical experience in data package development, judgement in use of expert statements and data waiving;
  • Selection, contracting and monitoring of studies compliant with guidelines and national good laboratory practice (GLP), to ensure a high quality scientific report for submission Robust Study Summary (RSS) writing using IUCLID for the submission of dossiers through R4BP;
  • Regulatory toxicology experience and know-how crucial with ever-increasing consideration of hazard-based classification criteria;
  • Risk assessments for human and environmental health;
  • Excellent rapport with European Regulatory Authorities.
 Contact LKC to discuss your requirements.

Related Information

Contact LKC

    LKC Switzerland Ltd
    Hauptstrasse 10
    P.O. Box 167
    4414 Füllinsdorf
    Phone: +41 (0) 61 906 8500
    Fax: +41 (0) 61 906 8509

      • Annex I
      • National approvals
      • re-review

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