“We are committed to
delivering the best results!”
Our experienced project management team works closely with you to deliver on time, on budget, and to the highest quality standards. You will have a primary point of contact who will guide you through every stage of the project, overseeing the team and tasks from design and development to manufacturing and market launch.
Design &
Development
At Haselmeier, we turn innovative ideas into award-winning medical devices. Our collaborative approach integrates your insights, market feedback and patient needs to create tailored solutions.
Whether using our highly standardized product platforms or a completely bespoke development, our expertise in design, planning, development, prototyping and testing ensures exceptional performance and safety. From concept to market launch, we deliver high-quality, compliant medical devices that meet the highest standards.
Human Factors
Human factors studies ensure that every device is designed with the end user in mind. By analyzing user interactions, safety, and ergonomics, we optimize our products for ease of use and efficiency. This approach reduces errors and improves safety, ensuring that our devices meet the highest standards of usability and performance.
We turn complex requirements into user-friendly solutions that excel in real world conditions.
Strong Intellectual
Property (IP)
Haselmeier and medmix’s robust and comprehensive IP portfolio is the foundation of our innovation.
Protected by our dedicated in-house team of experts, our strong IP framework not only secures our advanced technologies, but also enables us to deliver distinctive solutions that drive our customers’ success and give them a competitive advantage.
Regulatory Affairs
Regulatory Affairs are essential to ensuring that medical devices and pharmaceuticals meet all required standards and regulations for market access and patient safety.
Our Regulatory Affairs professionals plus a network of consulting specialists help you to manage the complex processes of product registration, compliance, and ongoing regulatory updates to place your products on the global markets.
Risk Management
In medical device development, effective risk management is essential to ensure safety and regulatory compliance.
At Haselmeier, we address potential risks at every stage – from process development and component qualification to device assembly, final assembly, combination products, labeling and secondary packaging. By addressing risks at every stage, we effectively minimize and manage them to ensure reliable results.
Drug Onboarding
Process
Developing a stable pharmaceutical product is just the beginning. The fill and finish process, a critical phase in the manufacturing of injectable drugs, requires specialized expertise. We partner with trusted experts to support you through every step of this process toward drug onboarding.
We ensure that your drug integrates seamlessly with our medical device, guaranteeing full compatibility with the device’s materials and mechanisms.