- Training
- November 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- June 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- November 2026
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Report
- August 2026
- 181 Pages
Global
From €3168EUR$3,545USD£2,708GBP
€3520EUR$3,939USD£3,009GBP
- Report
- August 2026
- 198 Pages
Global
From €3168EUR$3,545USD£2,708GBP
€3520EUR$3,939USD£3,009GBP
- Report
- August 2026
- 478 Pages
Global
From €5228EUR$5,850USD£4,469GBP
- Report
- May 2026
- 140 Pages
Global
From €4245EUR$4,750USD£3,628GBP
- Report
- May 2026
- 180 Pages
Global
From €4245EUR$4,750USD£3,628GBP
- Training
- October 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- April 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- March 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- February 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- February 2027
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- October 2026
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2026
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2026
- 2 Days
Global
€1573EUR$1,822USD£1,299GBP
€1815EUR$2,102USD£1,499GBP
- Training
- September 2026
- 2 Days
Global
€1815EUR$2,102USD£1,499GBP

The Marketing Authorization market is a key component of the Drug Discovery process. It is the process of obtaining approval from regulatory authorities to market a drug or medical device. This process involves submitting a dossier of data to the relevant regulatory body, which is then reviewed to ensure the product meets safety and efficacy standards. The dossier includes pre-clinical and clinical data, manufacturing information, and other relevant information. The process also includes post-marketing surveillance to ensure the product continues to meet safety and efficacy standards.
Companies in the Marketing Authorization market include AbbVie, AstraZeneca, Bayer, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, Merck, Novartis, Pfizer, and Sanofi. Show Less Read more