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GMP, GDP, quality and compliance: 24 audio courses for your whole company
GMP, GDP, quality and compliance is one of the topics Pharma Lectures covers in depth: 24 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 €2,340 for the whole company and a free sample module is available for every title.
The 24 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.
- ICH Q10 for a company that is not Pfizer: a Pharmaceutical Quality System built from scratch12 modules · 2 h to 10 h · QA, management · free sample module €4,680€7,488€11,700
- Deviation, CAPA, root cause: the investigation a European inspector actually believes10 modules · 1 h 40 min to 8 h 20 min · QA, production · free sample module €3,900€6,240€9,750
- Change control and ICH Q9 risk management: doing it daily, not just for the audit8 modules · 1 h 20 min to 6 h 40 min · QA, production · free sample module €3,120€4,992€7,800
- Audit or be audited: supplier qualification the way Europeans do it to you10 modules · 1 h 40 min to 8 h 20 min · QA, purchasing · free sample module €3,900€6,240€9,750
- Proving the process: process validation, cleaning validation and continued process verification12 modules · 2 h to 10 h · Production, QA, engineering · free sample module €4,680€7,488€11,700
- Does your method actually work: analytical method validation and transfer, ICH Q2(R2) and Q1410 modules · 1 h 40 min to 8 h 20 min · QC · free sample module €3,900€6,240€9,750
- Stability studies for the EU and ICH zones: design, storage, reporting, no month-36 surprises8 modules · 1 h 20 min to 6 h 40 min · QC, RA · free sample module €3,120€4,992€7,800
- OOS and OOT results: the investigation an inspector expects, not the retest they dread6 modules · 1 h to 5 h · QC, QA · free sample module €2,340€3,744€5,850
- Computerised system validation and the move to the cloud: still validated, just elsewhere10 modules · 1 h 40 min to 8 h 20 min · IT, QA · free sample module €3,900€6,240€9,750
- Pharmaceutical microbiology and environmental monitoring: what grows, where, and why it matters10 modules · 1 h 40 min to 8 h 20 min · QC, production · free sample module €3,900€6,240€9,750
- ICH Q3D elemental impurities and residual solvents for API and finished dose6 modules · 1 h to 5 h · QC, RA · free sample module €2,340€3,744€5,850
- Not written down, did not happen: good documentation practice and batch record review6 modules · 1 h to 5 h · All technical staff · free sample module €2,340€3,744€5,850
- URS to PQ: qualification of equipment, utilities and facilities without the paper mountain10 modules · 1 h 40 min to 8 h 20 min · Engineering, QA · free sample module €3,900€6,240€9,750
- The European customer audit: the two days, the report, the response that keeps the contract8 modules · 1 h 20 min to 6 h 40 min · QA, management, sales · free sample module €3,120€4,992€7,800
- Hosting an EU or FDA inspection, on site and remote: roles, the back room, the answers8 modules · 1 h 20 min to 6 h 40 min · QA, management · free sample module €3,120€4,992€7,800
- SOPs people actually follow (and inspectors accept)6 modules · 1 h to 5 h · QA, all technical staff · free sample module €2,340€3,744€5,850
- Cold, but how cold: temperature-controlled storage and transport, mapping and excursions8 modules · 1 h 20 min to 6 h 40 min · Logistics, QA · free sample module €3,120€4,992€7,800
- Returns, recalls, complaints and falsified product: handling the bad days properly6 modules · 1 h to 5 h · QA, logistics, sales · free sample module €2,340€3,744€5,850
- Contamination control strategy under the new Annex 1: the document inspectors now ask for first10 modules · 1 h 40 min to 8 h 20 min · Production, QA · free sample module €3,900€6,240€9,750
- Continuous manufacturing and ICH Q13: for companies actually planning the step8 modules · 1 h 20 min to 6 h 40 min · Engineering, management · free sample module €3,120€4,992€7,800
- GMP for excipients: IPEC, EXCiPACT and what a pharma customer expects of your plant8 modules · 1 h 20 min to 6 h 40 min · Excipient suppliers · free sample module €3,120€4,992€7,800
- ICH Q7 without the coma: GMP for API, chapter by chapter15 modules · 2 h 30 min to 12 h 30 min · API staff · free sample module €5,850€9,360€14,625
- GMP for biologics: Part II, Annex 2 and where small-molecule habits go wrong12 modules · 2 h to 10 h · Biologics staff · free sample module €4,680€7,488€11,700
- GMP for investigational products and clinical supply: Annex 13 in practice8 modules · 1 h 20 min to 6 h 40 min · CRO, CDMO · free sample module €3,120€4,992€7,800
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
- Pharma industry foundations25
- Regulatory affairs by region31
- 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