In the pharmaceutical industry, compliance and quality assurance are critical to ensuring patient safety and regulatory approval. At ZR Engineering, we provide expert consultants to help you navigate the complex regulatory landscape, ensuring your operations meet GMP requirements and industry best practices.
Our expertise includes
Quality Assurance & Quality Systems
Implementing and optimizing QMS, SOPs, and compliance frameworks.
Validation & Qualification
Ensuring compliance in process validation, equipment qualification, and computerized systems validation.
Deviation & CAPA Management
Identifying risks, implementing corrective actions, and improving compliance strategies.
Stay ahead of regulatory requirements.
Whether you need support for regulatory inspections, process validation, quality assurance, or system improvements, our consultants bring hands-on experience to strengthen compliance and maintain product integrity.