Courses › Regulatory affairs by region
Latin America: Brazil ANVISA: registration, GMP certification of foreign sites and the inspection queue
What is in the course, module by module
12 one-hour audio modules. Each one ends with a short quiz. The course ends with an exam, 80% to pass.
The module list for this title is being written. Ask for the sample module and we send the outline with it.
Price for this title
One licence, 12 one-hour modules, every employee of the legal entity, 12 months. Smaller companies pay less.
| Company size | Price | Discount |
|---|---|---|
| Over 500 staff | €11,700 | full price |
| 50 to 500 staff | €7,488 | 36% off |
| Under 50 staff | €4,680 | 60% off |
Cheaper as part of a track pack or company library. Delivered within 72 hours of payment or the course is free.
Who this is for
Roles: Business development and export sales, Regulatory affairs, Quality assurance and Qualified Person,
Businesses: every kind of pharma company
Countries: every country track
What you receive
- One-hour audio modules. Listen on the commute, at the bench, in the car.
- Companion workbook. Exercises and checklists per module, ready to file.
- Full transcript. Searchable, printable, quotable in your procedures.
- Source for every fact. Each statement links to its guideline, regulation or paper, so an auditor can check it.
- Certificate per learner. Name, course, hours, guideline version, date.
- Auditable training record. Per-person export for your quality file, the document inspectors ask for under EU GMP Chapter 2.
English first. Other languages are available in test mode on request.
Request a free sample module