I am excited to share my enriching experience with Raaj GPRAC Pvt Ltd, where I completed three outstanding programs: Biomedical Quality Assurance, MDD to MDR Implementation, and Lead Auditor ISO 13485. Thanks to this training, I secured a role as a QA/RA Executive and collaborated with director Rajashree Ojha on implementing ISO 13485 certification at Smaform Engineering India Pvt Ltd, propelling my career in the medical device industry.
Subsequently, I honed my skills at Woundclot Private Limited as a QA Engineer, engaging in various quality management systems and regulatory compliance initiatives. These practical experiences allowed me to apply my knowledge effectively, enhancing my professional capabilities.
Raaj GPRAC Pvt Ltd is distinguished for its dedication to providing top-notch education and training. Director Ms. Rajashri Ojha's expertise, support, and generosity, alongside her team, offer invaluable opportunities for real-world experience in the medical device industry.
I wholeheartedly endorse Raaj GPRAC Pvt Ltd to individuals seeking to excel in the biomedical and regulatory domains. Their courses are not only informative but also transformative, fostering professional growth and excellence within the industry.
KanchanShailaja Bhavsar Biomedical Engineers
I want to express my gratitude for the opportunity to
complete the CTD-eCTD cource.
The curriculum provided me with a deep worldwide frameworks understanding of different type of modules, sections and type of submission to different Regulatory Authorities worldwide, also timeline of different type of submissions, Regulatory strategies etc. Special thanks to Ms. RAJASHRI SURVASE-OJHA madam for her guidance and support throughout. This course has been instrumental in expanding my understanding of regulatory frameworks worldwide.
Ankita Bisht Executive Regulatory Affairs - Sunpharma
I would like to express my sincere gratitude to RAAJ GPRAC Team for designing " Global Regulatory Affairs" course which has given me an opportunity to upgrade my knowledge and skills in Regulatory Affairs. The course material is very well structured, and suited to industry requirements. The regular interactive sessions also offered necessary guidance and support.
As rightly said by you " Empowers the Women for second career", I am confident that this course will definitely provide me an edge to pursue a career in Regulatory Affairs.
Thanks once again.
I have completed CTD –eCTD course from RAAJ GPRAC. It was full of learning and grooming oneself. Their study material was very helpful to me as it easy way to learn and understand the course. I am thankful to RAAJ GPRAC.
It was my immense luck and fortune to be the part of RAAJ GPRAC. I have established my leadership, time management and learning skills and have also been able to advance these skills to the whole new level.
I have done the course in regulatory affairs for medical device that provide in depth information regarding medical device regulations worldwide. Each and every chapter gives wide information through article and video.
I hope this course can be helpful to me giving new opportunities in medical device regulatory career.
