Regulatory Affairs Specialist - Medical Devices
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As a highly qualified and experienced pharmacist with a post-graduation degree in Pharmacy, I have developed a deep understanding of the pharmaceutical industry and regulatory environment. With a strong background in business development and regulatory affairs, I am a specialist in medical devices, able to navigate complex regulations to ensure compliance and facilitate market access. I have a proven track record of success in developing strategic plans for product development and launch, managing relationships with key stakeholders, and ensuring regulatory compliance at all stages of the product lifecycle.
With my expertise and passion for the pharmaceutical industry, I am dedicated to driving business growth and innovation in the medical device sector.
Experienced Regulatory Professional involved in product registration of medical devices manufacturer (including GE Healthcare, Canon, KA Imaging, Sakura, Canon DelftDI IT, Teleflex, Progetti, e.t.c.) in Pakistan. The product profile ranges from imaging devices, monitoring devices, therapeutic equipment, Software as Medical Device (SaMD), medical furnitures e.t.c.
Trained ISO 13485 Lead Auditor, EU MDR 2017/745, and ISO 14971
