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Pharma industry foundations: 25 audio courses for your whole company
Pharma industry foundations is one of the topics Pharma Lectures covers in depth: 25 audio courses, each sold as one licence that covers every employee of the legal entity for twelve months. Every course exists in three lengths, so a board member hears the briefing, a regulatory officer takes the standard run and the people at the bench get the expanded walk-through, and every length ends with the same recorded questionnaire. Each course below ships with a companion workbook, a full transcript, a source for every fact, a certificate per learner and the auditable training record an inspector asks for. Prices start at €1,950 for the whole company and a free sample module is available for every title.
The 25 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.
- Molecule to pharmacy shelf: how a medicine actually reaches a European patient6 modules · 1 h to 5 h · All staff, new hires · free sample module €2,340€3,744€5,850
- Who decides what in Brussels: EMA, national agencies, EDQM and the Commission, untangled6 modules · 1 h to 5 h · All staff · free sample module €2,340€3,744€5,850
- Four doors into Europe: centralised, decentralised, mutual recognition and national procedures8 modules · 1 h 20 min to 6 h 40 min · RA, BD, management · free sample module €3,120€4,992€7,800
- You own the licence, now what: the MAH's annual obligations, none of them optional8 modules · 1 h 20 min to 6 h 40 min · RA, QA, management · free sample module €3,120€4,992€7,800
- GMP without the coma: EudraLex Volume 4, chapter by chapter, in plain English20 modules · 3 h 20 min to 16 h 40 min · All technical staff · free sample module €7,800€12,480€19,500
- GDP without the coma: the 2013 EU Good Distribution Practice guideline, article by article12 modules · 2 h to 10 h · Traders, logistics, QA · free sample module €4,680€7,488€11,700
- The signature that stops a batch: what the Qualified Person actually does6 modules · 1 h to 5 h · Management, QA, BD · free sample module €2,340€3,744€5,850
- The Responsible Person for distribution: the duties, the liability, how to work with one5 modules · 50 min to 4 h 10 min · Traders, wholesalers · free sample module €1,950€3,120€4,875
- Day one, the inspectors arrive: how an EMA or national GMP inspection really runs10 modules · 1 h 40 min to 8 h 20 min · QA, production, management · free sample module €3,900€6,240€9,750
- Every box tells a story: the Falsified Medicines Directive and serialisation, explained6 modules · 1 h to 5 h · Packaging, supply chain, IT · free sample module €2,340€3,744€5,850
- Pharmacovigilance for people who are not pharmacovigilance: the QPPV, explained6 modules · 1 h to 5 h · Management, BD, PV · free sample module €2,340€3,744€5,850
- Is it a drug or a device: combination products and when MDR takes over6 modules · 1 h to 5 h · RA, BD · free sample module €2,340€3,744€5,850
- Who sets the price of a pill: pricing and reimbursement in Europe's big markets10 modules · 1 h 40 min to 8 h 20 min · BD, finance, management · free sample module €3,900€6,240€9,750
- Hospital tenders in Europe: how public procurement of medicines works, and who wins it12 modules · 2 h to 10 h · BD, finance · free sample module €4,680€7,488€11,700
- Selling before the licence: named-patient and unlicensed supply, the legal routes8 modules · 1 h 20 min to 6 h 40 min · BD, RA, traders · free sample module €3,120€4,992€7,800
- Europe is not one market: generics country by country, from Germany to the Balkans15 modules · 2 h 30 min to 12 h 30 min · BD, management · free sample module €5,850€9,360€14,625
- The clause that costs you the batch: European contract law for supply, quality and distribution10 modules · 1 h 40 min to 8 h 20 min · BD, legal, management · free sample module €3,900€6,240€9,750
- Quality Agreements and Technical Agreements: every clause, and why it is there6 modules · 1 h to 5 h · QA, BD, CDMO staff · free sample module €2,340€3,744€5,850
- Data integrity: ALCOA+, audit trails and the gaps inspectors find first8 modules · 1 h 20 min to 6 h 40 min · QC, QA, IT, production · free sample module €3,120€4,992€7,800
- Annex 1 (2022) for sterile manufacturing: what changed, and what inspectors ask now12 modules · 2 h to 10 h · Production, QA, engineering · free sample module €4,680€7,488€11,700
- Nitrosamines: the impurity that cleared half a shelf, and how to stay off the recall list6 modules · 1 h to 5 h · QC, RA, API staff · free sample module €2,340€3,744€5,850
- Sustainability paperwork that wins audits: CSRD, EcoVadis and PSCI for pharma suppliers8 modules · 1 h 20 min to 6 h 40 min · Management, QA, sales · free sample module €3,120€4,992€7,800
- Computers in a GMP world: Annex 11, GAMP 5 and the EU AI Act, explained for pharma8 modules · 1 h 20 min to 6 h 40 min · IT, QA, validation · free sample module €3,120€4,992€7,800
- Pharma English: deviations, CAPAs, emails and reports a European reader believes10 modules · 1 h 40 min to 8 h 20 min · All staff · free sample module €3,900€6,240€9,750
- Business English for pharma sales: the calls, meetings and negotiations you cannot wing12 modules · 2 h to 10 h · BD, sales, marketing · free sample module €4,680€7,488€11,700
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 topics
- Regulatory affairs by region31
- GMP, GDP, quality and compliance24
- Pharma export and key account management16
- Pharma sales skills and selling across cultures159
- Pharma training by country80
- Pharma training by line of business60
- Pharma training by role48
- Country and business playbooks120
- Custom in-company pharma courses5
All topics, countries, lines of business and roles
Request a free sample module