AP Quality & Compliance's team understands the regulatory requirements which enable our teams to recommend and/or provide plans, methods or solutions to meet your company’s complex business environment.
Whether you are looking for complete program management, project management or the ability to supplement your staff with just one or a whole team of compliance experts to work under your direction, AP Quality & Compliance can respond quickly to meet your needs.
Full Program management
AP Quality & Compliance has the resources to take on a complete program ensuring the efficient coordination, communication and project completion on time and within budget. We have the resources, secure space, equipment and flexibility to ramp up to meet even the most demanding of projects.
Contact us to learn about how we can assist you with managing your next program.
AP Quality & Compliance is very proficient at managing specific projects or parts of projects associated with ensuring your quality needs are met and in full compliance with regulations and requirements. Our team of professionals have a broad understanding of and expertise in a variety of medical, pharmaceutical validation, compliance and regulatory requirements.
At our facility, we can provide the secure space, equipment and staff to handle most projects. We have the resources, secure space, equipment and flexibility to ramp up to meet even the most demanding of projects. (Available at our location or at customer location).
Contact us to see how we can assist you in meeting your needs.
Consultant Resources (Supplemental)
AP Quality & Compliance, as part of our full workforce solutions services has the capacity to recruit and provide resources to work at your facility under your supervision. Our vast network of consultant resources enable us to meet the most challenging of requirements that our customers ask of us in locations around the world.
Contact us to learn how we can help you meet your project deadlines.
Scope of Services
Life Science Quality Systems Design, Development and Implementation, Audit, Assessment, etc.
Validation Engineering and Remediation, Process Document Review and Creation, Validation Processes, Automation, Cleaning, Test, Laboratory, and Computerized Systems, etc.
Quality System Review, Regulatory Submission Review Services, Risk Assessment, Gap Analysis, etc.
Medical Device Capital Equipment Design, Plant Automation, Product Scale-up and Commercialization, etc.