The pharmaceutical industry is a cornerstone of healthcare, dedicated to developing, manufacturing, and distributing drugs to support global public health. Pharmaceutical ingredient and drug manufacutring operates under strict regulations encompassing drug testing, approval processes, and quality control to ensure safety and efficacy.
High quality, safe, pure healthcare products can only be assured by implementing robust and effective management systems and processes. Eurofins Assurance experts in the healthcare field provides audit and certification, training and advisory services focused on safety and quality management systems, process optimisation, risk and cost reduction and brand protection.
Whether you are identifying new drug targets, obtaining regulatory approval from government agencies, optimizing techniques in drug discovery and development, manufacturing under Good Manufacturing Practices or pursuig distribution and post market surveillance, you can find your solutions here.
Deliver target-based and data-based claims around products and processes against sustainability commitments and goals.
We can provide virtual or in-person trainings, customised to your needs, on quality standards, regulatory evolution to technical expertise.
Our team with robust pharmaceutical compliance knowledge can help you to achieve continuous improvement and improve quality and regulatory compliance by solutions including gap analysis, and consulting on implementation of quality system or new regulations and quality investigations. Check out advisory service for pharmaceutical industry.
Visit our report library to search for available shared audit reports, or request a new audit instantly!
Our GXP audit is accredited for ISO 9001, showcasing our commitment and achievement to quality excellence!
Ensure to source and manufacture responsibly, meeting social and ethical compliance.