GLP / GCP - Quality Program
BioScience Laboratories, Inc. maintains a GLP/GCP quality program that ensures our clients' studies are performed well and in compliance with regulatory requirements. Each study undergoes a quality review prior to initiation, in-process audits, and a final quality audit upon completion. A continuous quality improvement process is in place to address any discrepancies and consistently enhance the value of our services.
Our laboratory facility is registered with the FDA. In addition, in its nearly two-decade history, our Quality Assurance program has experienced more than 200 successful audits performed by federal agencies, third-party auditing firms, and dozens of our clients. We invite you to visit and audit our facility to verify, first-hand, how our quality program assures that your study is performed accurately and in compliance.
Partnering with a laboratory that understands the regulatory requirements and intra-industry competitive pressure can mean the difference between the success and failure in new product approval and product acceptance by end-users. BioScience Laboratories, Inc., enjoys strong, professional relationships with the CDC, EPA, FDA, USDA and Health Canada; these relationships are passed on as added value to our clients in the form of adherence to the most current regulations and approved practices.
To ensure that you receive the most reliable, high-quality laboratory services, all studies at BioScience Laboratories are performed in accordance with the relevant standards and methods specified by the following: