№ lp_1_32186
A guidance document detailing standardized terminologies and codes for reporting adverse events related to medical devices and in-vitro diagnostics.
Year: 2020
Region / City: International
Topic: Medical device regulation
Document Type: Final Document
Organization / Institution: International Medical Device Regulators Forum (IMDRF)
Author: IMDRF Adverse Event Terminology Working Group
Intended Audience: Regulatory authorities, medical device manufacturers, healthcare providers
Period of Validity: Not specified
Approval Date: 18 March 2020
Date of Changes: Not specified
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.

Don’t have cryptocurrency yet?

You can still complete your purchase in a few minutes:
  1. Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
  2. In the app, tap Send.
  3. Select network, paste our wallet address.
  4. Send the exact amount shown above.
After sending, paste your TXID (transaction ID) and your email to receive the download link. Need help? Contact support and we’ll guide you step by step.