The Pharm Bureau

The Pharm Bureau is dedicated to the FDA and internationally regulated industries providing cost effective, comprehensive and regulatory sound Validation and Compliance services to the Pharmaceuticals, Biotechnology, Vaccines, Blood & Biologics, Medical Devices, Animal Health, Medical Diagnostic, Combination Products industries. We provide Auditing, Validation, Qualification and Commissioning Services committed to the highest level of service and expertise required to meet all of your validation needs of validation and quality systems services for your cGMP/GLP/GXP facility. We are committed to providing your company with an integrity based solution to ensure your company is regulatory compliant and have the tools to ensure a continued path in the future in maintaining this direction. We prepare and execute validation IQ/OQ/PQ protocols, compliance documentation for equipment, utilities, processes, laboratory instruments, and computer systems. We also perform Gap Assessment and Remediation Planning, as well as Internal and External Auditing by FDA Auditor trained personnel, evaluation of current SOP’s, WI’s, Policies and all other areas to ensure that your QMS and regulatory facilities are sufficient to meet current regulations. We will deliver a cost effective, regulatory sound validation and compliance strategy to you project or for your corporate approach to compliance. We invite you to contact us to discuss your needs and the solutions we can provide to you.