JPL is committed to providing clients with the highest quality in analytical (chemistry, chromatography, microbiology), consulting, stability, development and validation services. We strive to respect client timelines, as well as the accuracy and integrity of all data generated while performing tests or projects. We pride ourselves in ensuring our facility, equipment, records and procedures are maintained in accordance with applicable regulatory and compendial requirements with respect to the Client’s specifications.
JPL offers consulting services for quality assurance and regulatory requirements to the pharmaceutical industry. We assist our clients in various aspects of their quality assurance programs, including assisting them in meeting GMP requirements, developing Standard Operation Procedures (SOP) and preparing for regulatory inspections.