AlvaMed is an ISO 13485 certified consulting and outsourcing firm to the medical device industry.
We provide the full breadth of compliance services to our clients: quality assurance, quality system development, regulatory, and clinical services.
Since 2002, AlvaMed has helped large and small companies address compliance needs and bring new products to market.
what we do
We work for our clients in a number of different ways based upon their preference.
- Medical device registration and approval
- QMS compliance
- Regulatory affairs support
- Clinical affairs support and outsourcing
We provide a range of services from reviews and opinions to small and large projects to ongoing support on a short term or long term basis.
We can become your company’s regulatory, quality and clinical affairs functions.
We remove the need to hire on full-time staff, provide greater flexibility and eliminate investments in extra infrastructure.
We have a breadth of expertise without the large overhead and high cost. Alvamed has a team that will be there for you in the future, as opposed to engaging different individual experts each time.