About Us
Veritas Quality Solutions: Your Partner in Quality Assurance
Founded in 2025, Veritas Quality Solutions was established with a singular vision: to be the premier consultancy for Medical Device Regulations (MDR), Quality Management Systems (QMS), and global regulatory compliance. As Your Partner in Quality Assurance, we are dedicated to empowering medical device manufacturers to navigate the complex and evolving landscape of international regulations with confidence and precision.
Pioneering Regulatory Excellence in Pakistan
We take immense pride in being pioneers within the Pakistani market. Our team was the first to successfully guide clients through the stringent requirements for MDR Class IIa, IIb, and Is certifications, achieving this milestone in collaboration with SGS Belgium. This foundational success has established us as a trusted leader in the field.
Our expertise extends across the full spectrum of medical device classifications, from the legacy Medical Device Directive (MDD) to the current Medical Device Regulation (MDR), covering Class I, Class Ir, Class IIa, and Class IIb products. We maintain robust relationships with a network of renowned Notified Bodies, including Intertek and other client-specific organizations, ensuring we can tailor our approach to meet your unique certification needs.
Your Gateway to Global Markets
Our mission is to facilitate seamless market access for our clients across the globe. We have a proven track record of successfully helping numerous companies register their medical devices in key markets, including:
Middle East: Kingdom of Saudi Arabia (KSA), UAE, Turkey, Azerbaijan
Americas: Brazil, USA
Europe & UK: Europe, United Kingdom
Asia-Pacific: Indonesia, Malaysia, China, Australia, New Zealand, Thailand
Eurasia: Russia
Comprehensive Support and Authorized Representation
To further support your global ambitions, we offer comprehensive Authorized Representative services. Through our established panel of experts, we provide seamless access to:
European Authorized Representative (EC REP)
Swiss Authorized Representative (CH REP)
UK Responsible Person (UK REP)
US Agent Services
On-Site Audits and Unwavering Commitment
Our commitment to quality extends beyond documentation. Our experienced team conducts on-site audits on behalf of our clients in key manufacturing hubs, including Pakistan, the Kingdom of Saudi Arabia (KSA), the UAE, and Turkey. This hands-on approach ensures that your facilities and processes consistently meet the highest standards of regulatory compliance.
At Veritas Quality Solutions, we are more than a consultancy; we are your dedicated partners in quality assurance. Let us leverage our vast experience and global network to bring your medical devices to the world.
Meet Your Regulatory Expert
Imran Yousaf serves as the Principal Consultant of Veritas Quality Solutions, a premier medical device regulatory consultancy established to guide manufacturers through the complexities of global compliance. Drawing on deep expertise spanning a wide range of therapeutic specialties, Imran and his accomplished team deliver authoritative support on MDR transition, technical documentation, clinical evaluation, UK Responsible Person obligations, regulatory compliance, and related disciplines. His driving purpose is to simplify and accelerate regulatory pathways, enabling companies to dedicate their resources and attention to what matters most, innovation.
