Master advanced regulatory writing for pharma/biotech. Learn to create clear, compliant documents (CSRs, CTDs, IBs) adhering to FDA, EMA, and international regulations. Develop skills in data interpretation, argument construction, and regulatory compliance through practical exercises. Ideal for medical writers, clinical research, and regulatory affairs professionals.
Learn more| Has discount |
![]() |
||
|---|---|---|---|
| Expiry period | Lifetime | ||
| Made in | English | ||
| Last updated at | Sat Aug 2025 | ||
| Level |
|
||
| Total lectures | 7 | ||
| Total quizzes | 0 | ||
| Total duration | Hours | ||
| Total enrolment |
0 |
||
| Number of reviews | 0 | ||
| Avg rating |
|
||
| Short description | Master advanced regulatory writing for pharma/biotech. Learn to create clear, compliant documents (CSRs, CTDs, IBs) adhering to FDA, EMA, and international regulations. Develop skills in data interpretation, argument construction, and regulatory compliance through practical exercises. Ideal for medical writers, clinical research, and regulatory affairs professionals. | ||
| Outcomes |
|
||
| Requirements |
|