Every therapeutic goods and health sciences business needs to understand the regulatory requirements and possess a robust quality culture. Our team of highly experienced pharmaceutical industry professionals have a wealth of expertise to help you navigate the regulatory framework and implement the right solutions for you to maintain compliance and generate performance improvements.     

You will benefit from our core capabilities in Regulatory Affairs, Quality Management Systems and Technical Operations (Engineering and Operations improvements) for the delivery of regulatory approvals and the implementation of qualified systems, processes and training across a diverse range of the health sciences:

• Medicine Manufacturing Operations - Topical/Oral/Solid Dose and Sterile Injectables

• Medical Device Manufacturing

• Biotech Operations

• Health Science Facilities

• Blood and Tissue Banks

Our purpose is to ensure that you receive the best service to meet your project’s needs.