regulatory for medical device

Hi I am Msc in medical biotechnology and microbiology. I have 7 years of research and writing experience and have worked on PhD level thesis projects, published papers in peer reviewed journals and have also worked with several companies on creating research based reports and formulating novel products. I have excellent academic writing skills and statistical analysis skills in R , spss, excel to complete any assignment in high quality. Looking forward to discussion, Best Regards, Suyash

Hi, I am a medical graduate, currently doing my PG in medicine and neurology. I love to search and research on medical topics... Let's talk to proceed. Regards. Dr. Asad

Greetings! I am law graduate and Certified ISO Lead Auditor. I have drafted number of SOPs in MDD regime and closely following, creating SOPs for MDR & IVD Regulations. Please PM me to discuss further. Thank you.

A proposal has not yet been provided

iam experienced pharmacist

Medical student in finishing year

I Am a process consultant and 6Sigma practitioner. Exposed to ISO 9001 STANDARDS And related Documentation requiements. During every process improvements, we ensure the documents are corrected and updated to related safety , regulatory requirements . I have been involved and exposed to writing standard documents for electronic related testing at my earlier organisation. In addition, i am aware of Standard work process sheets in line with Lean manufacturing practices for assembly line. I look forward to this opportunity