Regulatory Advisor and PRRC
Nida Ali joined Lifelab in 2022 as the Regulatory Advisor and PRRC. Nida is a qualified lawyer who graduated from the Queen Mary University of London. She has been a Director of Kounter Intuitive Technologies since 2014 and has been creating Clinical Evaluation Reports for the last 6 years, having certifications on MEDDEV 2.7.1 REV.4 and EU MDR 2017/745.
Nida has worked extensively on FDA 510K regulations for medical devices and provided strategic support in regulatory affairs, and post-market product surveillance. She has also completed quality assurance in CE marking of EU Class 1, 11a, 11b or 111 medical devices by writing Clinical Evaluation Reports providing clinical evidence of the art for medical treatment and its safety and performance and response to notified body feedback.
Recently, Nida has been working on a Government of Pakistan-funded project under the special directive of the Prime Minister’s Office of Pakistan for the development of the purpose-built Medical Devices Development Centre (MDDC), National Centre of Excellence for the indigenous production of Bare-metal Cardiac Stents, Drug Eluting Stents, Angioplasty Balloon Catheters, and artificial heart valves. Nida has also created their Technical Documentation according to MEDDEV 2.7.1 REV.4 and then updated to MDR (EU) 2017/745.