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Training for Regulatory affairs in pharma: 229 audio courses

People working in Regulatory affairs in a pharma company need training that respects their time and their role. Pharma Lectures has 229 audio courses written for them, each in three lengths, from a briefing of ten minutes a module to an expanded walk-through for the people who run the procedure every day. Every course is one licence for every employee of the legal entity for twelve months, so Regulatory affairs can take the same title as the rest of the company and the training record stays in one place. Each course ships with a companion workbook, a full transcript, a source for every fact, a certificate per learner and a recorded questionnaire per module for the quality file. Prices start at €1,950 and a free sample module is available for every title.

Request a free sample module See the 229 courses

The 229 courses, with the price for your company size

Prices are for the whole company, 12 months. Pick your company size once; the site remembers it.

How a Pharma Lectures course works

Every title is one licence for the whole legal entity, twelve months, every employee. Each module exists in three lengths: 10, 25 or 50 minutes, by role. Each module ends with a recorded multiple-choice questionnaire, so the training record is complete for the auditor. Delivered within 72 hours of payment.

Audio modules in all three lengths, included in every purchase. The briefing for the board and the sales floor, the standard run for regulatory and quality, the expanded walk-through for the bench. One price buys all three; each person takes the length their role needs. Listen on the commute, at the bench, in the car.
Made to be listened to. A narrator with character, a story in every module and real examples from the buyer's side of the table. Not a read-out of the guideline that puts the room to sleep.
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.

Other roles

All topics, countries, lines of business and roles

Request a free sample module

Training for Regulatory affairs in pharma: 229 audio courses

The 229 courses, with the price for your company size

How a Pharma Lectures course works

Other roles

Hear one full module before you spend a cent. Send your company and the role you want trained, and a complete sample module comes back with its workbook and transcript.