There are numerous types of non clinical laboratories. These include Pharmaceutical Quality Control Labs, Research and Development Labs, toxicology testing facilities, central labs to support clinical trials and even manufacturing facilities that work on a lab scale. These laboratories may be associated with animal care facilities, or may handle pathogens, tissues or genetically manipulated organisms. Many of these laboratories are required to comply with GMP or GLP regulations and other rules related to safe handling of radioactive, recombinant, toxic, flammable or biologically active material.

PSC can assist you with our laboratory expertise. Our services range from providing you with skilled lab personnel to completely designing or redesigning your facility. We provide:

• Training in complying with OECD GLP and with 21 CFR Part 58.
• Assistance in developing laboratory quality systems including policies on handling Out Of Specification results, setting up a robust chain of custody, calibration and maintenance policies, management of control article (reference samples), retention and retrieval policies, raw data and electronic record rules.
• Assistance with documentation – SOPs, records, log books, study protocols.
• Services for the migration of manual systems or legacy systems into modern automated laboratory information management systems.
• Assistance with your initial and ongoing stability programmes including training, protocol and SOP development, results and trend analysis and photostability testing.
• Design and Design Review of laboratories.
• Laboratory and Quality Systems audits.

If you have a need for our laboratory services, please Contact Us.