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Our advanced technical and analytical expertise, rigorous testing, regulatory review, and advanced facilities will help you attain faster regulatory approval.

Intertek offers a diverse range of contract analytical research, consulting, and testing services to support global pharmaceutical and biotech industries developing and manufacturing new medical devices, and related healthcare products.

Our Medical Device Services

• Medical Device Testing and Certification
• Management Systems Auditing and Certification
• Notified Body services for CE marking
• Other global or local product certifications
• RoHS Directive (2011/65/EU)
• Regulatory consulting and project management
• Regulatory education

We combine expert understanding of local and regional regulatory issues relating to medical devices with the efficiency and cost-effectiveness of our global network of testing labs. We go beyond testing, inspecting and certifying products; we help customers improve performance, gain efficiencies in manufacturing and logistics, overcome market constraints, and reduce risk. We’ve earned a reputation for helping our customers increase the value of their products, gain competitive advantage, and develop trusted brands.  Through our services we help our clients to minimise the adverse health and environmental impact of their products and processes for the benefit of society as a whole.

Intertek is the industry leader with over 35,000 people in 1,000 locations in over 100 countries. Whether your business is local or global, we can ensure your products meet quality, health, environmental, safety, and social accountability standards for virtually any market around the world.  We hold extensive global accreditations, recognitions, and agreements, and our knowledge of and expertise in overcoming regulatory, market, and supply chain hurdles is unrivaled.