Professional Services
At QPharma, we specialize in providing comprehensive professional services tailored to the unique needs of the life sciences industry and individual client. Including compliance consulting, software validation, equipment qualification, project management, facility commissioning, quality system auditing, staff augmentation, and training. We offer a full suite of services to ensure regulatory compliance and operational excellence.
Our GxP Professional Services Offerings
Compliance Consulting
Our team of experts offers strategic guidance and consulting services to help your organization navigate complex regulatory requirements. From FDA compliance to international standards, we provide the expertise needed to ensure adherence to the appropriate regulatory standards. Our consultants analyze each customer’s circumstances and will offer viable solutions to obtain or maintain compliance.
Software Validation
We assist in validating software systems to ensure compliance with regulatory standards. Our validation services cover a wide range of systems and processes, including customer relationship management (CRM), electronic document management systems (EDMS), laboratory information management systems (LIMS), warehouse management systems, and automated manufacturing processes.
Project Staffing
Need skilled professionals to support your GxP projects? Our project staffing services provide access to qualified personnel with expertise in regulatory compliance, validation, quality management, and more. Whether you need short-term support or long-term staffing solutions, we've got you covered.
Quality Systems Consulting
Are you expecting the FDA to visit? We can help you prepare by performing a comprehensive audit of your existing Quality System. Starting with the Quality Manual, moving to your policies and procedures, and finally training. We will ensure you have the appropriate level of detail for your facility and products. Based on the comprehensive audit, we will be able to. • Identify the levels of compliance needed • Perform a gap analysis to find greatest risks of FDA action • Map production processes to locate inefficiencies • Develop and help implement comprehensive remediation actions, and If necessary, we can implement a full Quality System from scratch.