A distinguished public health professional with extensive experience in the pharmaceutical and health sciences sectors. Dr. Rashid holds a Ph.D. in Pharmacy and an M.P.H. in Public Health, providing a strong foundation in quality management systems, including ISO 13485. His career highlights significant contributions to health initiatives, training, and research, with a focus on enhancing national...
Experience: 39+ years
Abdur Rashid provides regulatory consulting services to clients in:
Possesses a strong academic foundation with a Ph.D. in Pharmacy from China Pharmaceutical University and an M.P.H. in Public Health from Sarhad University of Science and Information Technology. Further academic depth includes an M.Phil in Pharmacy from Bahauddin Zakariya University. This robust educational background provides a comprehensive understanding of pharmaceutical sciences and public health, crucial for navigating complex regulatory landscapes in the medical technology sector.
A seasoned professional with extensive experience in public health and the pharmaceutical industry. Their career has been dedicated to advancing health initiatives and strengthening health systems, demonstrating a deep understanding of operational and strategic aspects within the healthcare domain. They have a proven track record in contributing to significant health programs and capacity-building efforts, highlighting their ability to drive impactful projects and deliver results in diverse healthcare settings. Their experience is directly applicable to supporting medical device companies in understanding and integrating into global health frameworks.
A distinguished public health professional with extensive experience in the pharmaceutical and health sciences sectors. Dr. Rashid holds a Ph.D. in Pharmacy and an M.P.H. in Public Health, providing a strong foundation in quality management systems, including ISO 13485. His career highlights signifi...
With 39 years of experience, Abdur Rashid is a highly accomplished and dedicated public health professional who specializes in regulatory affairs for medical devices. He possesses a strong academic foundation with a Ph.D. in Pharmacy and an M.P.H. in Public Health, complemented by a robust understanding of quality management systems, including ISO 13485. His extensive background in public health, pharmacy, and specialized training in medical device quality management systems makes him uniquely valuable for medtech companies seeking expertise in global health and regulatory affairs. He has a proven track record in contributing to significant health programs and capacity-building efforts, highlighting his ability to drive impactful projects and deliver results in diverse healthcare settings. His experience in navigating complex health-related regulatory environments, including outbreak investigation and health systems strengthening, makes him a valuable resource for medtech companies seeking to align their products with public health needs and regulatory expectations.
This analysis is generated by Cruxi AI using public information and may not capture the full scope of the consultant's experience.
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