- Training
- November 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- June 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- November 2026
- 2 Days
Global
€1855EUR$2,079USD£1,499GBP
- Training
- November 2026
- 2 Days
Global
€1855EUR$2,079USD£1,499GBP
- Report
- September 2026
- 186 Pages
Global
From €3274EUR$3,545USD£2,739GBP
€3638EUR$3,939USD£3,043GBP
- Report
- September 2026
- 186 Pages
Global
From €3274EUR$3,545USD£2,739GBP
€3638EUR$3,939USD£3,043GBP
- Report
- October 2026
- 478 Pages
Global
From €5403EUR$5,850USD£4,519GBP
- Report
- May 2026
- 140 Pages
Global
From €4387EUR$4,750USD£3,670GBP
- Report
- May 2026
- 180 Pages
Global
From €4387EUR$4,750USD£3,670GBP
- Training
- October 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- September 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- April 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- March 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- February 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- February 2027
- 2 Days
Global
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- October 2027
- 2 Days
Europe
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Training
- March 2027
- 2 Days
Europe
€1607EUR$1,801USD£1,299GBP
€1855EUR$2,079USD£1,499GBP
- Report
- August 2022
- 30 Pages
Global
From €3002EUR$3,250USD£2,511GBP

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