MIQARA is proud member of:

• Swedish Standards Institute SIS TK355 and International Organization for Standardization ISO TC210

• Strategic Advisory Group on Healthcare Standards (SAG Healthcare) - Artificial Intelligence

• MEDEA - National Association for Medical Device Consultants

• TOPRA - The Organisation for Professionals in Regulatory Affairs

• Apotekarsocieteten - Medical devices section

Note: Links to other web pages above

Supporting your company, our main goal

OFFERING VERSATILE CONSULTING

MANY YEARS OF EXPERIENCE

LEADERSHIP KNOWLEDGE

At MIQARA, we specialise in providing versatile and flexible support within Quality Assurance and Regulatory Affairs (QARA) for medical devices, in-vitro diagnostics, SaMD, combination products, and custom made devices, helping you to navigate the regulatory universe.
We are passionate concerning guiding companies through the complexity of regulations, from product development and all phases of the product lifecycle, to help enable and maintain market access for the benefit of patients.
Please see the services we provide.

Our deep understanding of the regulatory landscape enables us to guide your company in identifying the most suitable strategies and solutions for compliance. From structuring your quality management processes to executing efficient regulatory strategies, MIQARA is committed to the success and compliance of your medical devices or IVD products. Please read about our experiences.

We are looking forward to hearing from you.

Supporting your company, our main goal

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