Navigate through Global medical device regulations with ease.
If you are venturing out of your home market, you may find it difficult to navigate through the complex world of medical device regulatory requirements.
You will spend much of your time combing the internet, reading through group postings, asking regulatory agencies questions that may not directly provide the answers you need.
When it’s all said and done, you have wasted your precious time going in circles.
What if you can access the relevant information from a single Excel document? Imagine the time that you would save:
- Pick a country and region from a list and voilà! Out comes the regulatory information you need
- Find out who the regulatory authority for your chosen target market(s)
- Identify if your product needs safety certification in addition to the regulatory requirements
- Identify who can safety certify your device with the relevant accreditation
- Identify other regulatory requirements that may have cross-jurisdiction for your device
- Identify the classifications in your target market(s)
- Identify if your existing QMS/GMP are accepted in your target market(s)
- Know the industry terms and acronyms so you can better understand what you need
- Know the best route for product certification that will save you time and money
- Know what standards are used based on your target market(s)
- And more!
If you need a clear path to global medical device regulatory compliance, this document is for you.
For a limited time, you can reserve your own copy for only US$99.95. After this promotional offer, the price will double. A small investment even at double the price.
We expect this document to be completed by mid-December 2018. It’s a short wait to make your job easier.
Simply complete the short form below and you can process your order via Paypal.
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