The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
Eighty percent of drugs consumed in the Middle East are currently imported, but governments across the region are trying to change that by boosting domestic manufacturing and joint ventures and licensing deals, according to Frost & Sullivan’s analysis of the Gulf Cooperation Council pharmaceutical market. The reliance on drug and raw material imports, especially in Saudi Arabia and the United Arab Emirates, coupled with low R&D capability, are the main market constraints, Manisha Rawat said. International Pharmaceutical Regulatory Monitor