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Top Industry News
- Republic of Cyprus- CESP Mandatory Submissions
- Health Canada- Notice: Update to Clinical Trial Site Information Form
- SAHPRA- How to Respond to a GMP, GWP or GCP Inspection Report
- FDA- Adaptive Design Clinical Trials for Drugs and Biologics Guidance for Industry
- The AEMPS (Spanish Agency for Medicines and Health Products) Establishes as a Term Until June 30, 2020 for the Adaptation of the Labeling and Instructions for the use of Medical Devices as a Result of the Changes Made by a Possible Brexit