Streamline Your Compliance Process with the New CAPA Template – MDCG 2024-12
The MDCG 2024-12 template is a vital tool for [...]
Post-Market Surveillance (PMS): A Key Pillar for Compliance and Innovation in the Medical Device Industry
In the rapidly evolving field of medical devices, compliance with [...]
Is the FSC valid indefinitely, or does it have an expiration date?
If you’re a medical device manufacturer, understanding the validity of [...]
How to Obtain CDSCO Approval for Medical Devices
Obtaining CDSCO (Central Drugs Standard Control Organization) approval in India [...]
New Revision of European Medical Device Regulations: Towards Greater Transparency and Safer Access for All
In response to current challenges regarding the accessibility and [...]
Is the TGA Sponsor Responsible for the Quality or Safety of Your Products?
No, it’s essential to understand that in Australia, the [...]
Looking for an FDA Agent? 5 Key Factors to Consider
If you’re selecting an FDA Agent for the U.S. [...]
What is the IFU and why is it crucial for medical devices?
The Instructions for Use (IFU) is essential for every [...]
CMC Consulting Group celebrates tenth anniversary of CMC Medical Devices with a new corporate image
CMC Consulting Group, a leading holding company in regulatory [...]
