ABOUT THE SERVICE

Lancaster Laboratories has been providing analytical testing services to the Pharmaceutical, Medical Device and Food industries since 1986. Now, under the expert guidance and management of the same team who bring you excellence in service and innovation at Lancaster Laboratories, we are now pleased to offer our equipment validation services.

For many years the Quality Assurance team at Lancaster Laboratories has been providing an in-house equipment validation service to its own laboratories. We have now extended this service to our clients to compliment the analytical services they receive. Through our highly developed systems and qualified personnel, we are able to offer enhanced value to our clients by offering custom-made validation protocols, execution of those protocols and validation reports - all to cGMP standards.

Lancaster Laboratories Validation strives to exceed its customers' expectations through the use of a Quality System which is designed, built and maintained on the principles of customer satisfaction and continuous improvement. To this end, Lancaster Laboratories Validation operates under a Quality System certified to ISO9001:2000.

LANCASTER LABORATORIES VALIDATION

• Lancaster Laboratories Validation can prepare application-specific validation protocols or simply execute existing client procedures on a wide range of thermal processes and equipment.
• Thorough hands-on experience ensures that acceptance criteria are based on recognised
  international standards and guidelines. All validation work is performed accurately and efficiently under a firm contract basis.
• Study results are delivered in a well-organised report package and in a format tailored to meet your quality assurance needs.
• Lancaster Laboratories Validation ensures prompt delivery of the final reports and raw data crucial to the end point of validation work.

TAILORED VALIDATION PROTOCOL GENERATION

ACCURATE AND EFFICIENT VALIDATION EXECUTION

PROMPT DELIVERY OF FINAL REPORT PACKAGE

Lancaster Laboratories Validation staff are fully trained, qualified and experienced in all aspects of thermal equipment validation. Within Lancaster Laboratories validation reports have been subject to inspection by the IMB, FDA and other industry regulators.

We offer use of industry standard KAYE instruments (Validator 2000) specifically designed to satisfy your reporting needs as well as electronic record regulations defined by 21 CFR Part 11 and Annex II. All of our reference test equipment is independently calibrated (NIST) to ensure traceability, reliability and overall system accuracy.

Outsourcing the validation of your thermal process and laboratory equipment can eliminate extensive work in meeting your validation regulatory requirements.

Application, customer specific, tailor made protocols
Validation of your thermal processes and laboratory equipment
Fully trained, qualified and experienced personnel
Validation reports to meet or exceed your requirements