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Link China Solutions Ltd
Milton Hall
Ely Road, Cambridge
CB24 6WZ
United Kingdom
Phone: 0044(0)122 382 8215
Email: info@chinapharma.co.uk
  LCPS will work with reputation Chinese research institutes and organizations with advanced chemical and biological experimental equipments, function lab units, professional work team and strict SOP. We are able to execute standard operation and a reliable working process for each experiment. Provide a road map for safety assessment as an integral part of the development of new drugs and therapeutics, service covers Acute toxicity testing in pharmaceutical safety evaluation, Genotoxicity, Safety assessment of inhalant drugs, Immunotoxicology in pharmaceutical development, Large animal laboratory trial studies.
We facilitate the drug research and development company to manage the preclinical trial in China. The packages are drawn from the formulation, analytical, delivery system and preclinical expertise within the core-business. Minimalists ones can be provided for Proof of Principle in man (Phase I).
We offer the following preclinical services to clients:
  • Strategic planning
      > Establish focussed and attainable goals for all preclinical aspects of your development programme
      > Write strategic and tactical preclinical development plans to incorporate within your overall Product development plan
  • Preclinical efficacy and safety testing
      > Identify and write appropriate efficacy and safety testing strategies
      > Identify major academic/commercial service providers
      > Prepare, review and edit efficacy/safety test protocols
      > Write, review and edit preclinical data package(s) and report(s)
  • Safety testing (biocompatibility) - medical devices
      > Identify current safety database on materials intended for use in your medical device
      > Perform risk analysis with respect to intended human exposure
      > Identity commercial safety testing providers
      > Prepare, review and edit test protocols
      > Place and manage biocompatibility test programme
  >Write, review and edit data package(s) and report(s)
  • Project Management
      > Identify and integrate preclinical development programme into your fully integrated Product development plan
      > Manage academic/commercial service providers
      > Manage smaller subcontractors in support of service providers
      > Manage timelines and allocated budget
  • Quality Systems and Assurance
      > Prepare Quality policies in compliance with GLP
      > Write Standard Operating Procedures
      > Aid with the implementation of Corporate Quality Systems
 
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