Cheap Price - Great Service
Starting a medical device company can be a very expensive proposition – R&D eats up most of the budget and when its all said and done – there is typically very little left for regulatory clearance. Of course, regulatory approval is an absolute must even in terms of raising future funds for operations, production, etc.
Everyone wants a cheap price but nobody wants cheap service.
Looking for a cheap 510k submission service ? Go with a Company that has the experience and expertise you need.
That’s where Yakar Engineering comes in.
With offices in Israel and the US, Yakar Engineering provide high level Quality, Regulatory and Clinical Affairs services to startup companies & entrepreneurs, across a wide range of medical disciplines, in the most efficient and cost-effective manner.
Yakar Engineering boasts a multi-disciplinary team of highly experienced engineers, pharmacists, and regulatory experts. The team is driven by professional skill, industry experience and an exceptionally detailed knowledge of the medical device and pharmaceutical startup sectors.
Our regulatory experience and expertise covers the US, EU, China, MDSAP countries (Japan, Brazil, Australia, Canada) and Russia.
With a wide network of professionals around the globe, there’s no job we can’t handle, while being cognizant of our client’s requirements and financial situation.
Don’t pay top dollar to a second tier consulting firm. Give us a call or shoot us an email today.
Your satisfaction is our number 1 priority.