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All of our courses

Pharmacokinetic and Pharmacodynamic (PK/PD) Analysis in Drug Development

A practical introduction to pharmacokinetic and pharmacodynamic (PK/PD) analysis in drug development, covering PK processes, exposure-response relationships, and modeling approaches used in preclinical and clinical studies.

Ideal for professionals working in drug development, clinical research, regulatory affairs, and pharmacology.

Course Launch: 24 April 2026

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$840.00

$1,050.00

Outsourced Operations: Using Contract Facilities

A practical training on managing outsourced pharmaceutical operations, including CDMOs, contract laboratories, quality agreements, contractor oversight, and regulatory expectations from FDA, EMA, and EU GMP.

Ideal for professionals responsible for outsourcing, quality systems, regulatory compliance, and contractor management.

Course Launch: 24 April 2026

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$840.00

$1,050.00

Microbial Control Strategy: Managing Risks in Non-Sterile Manufacturing

A practical training on designing microbial control strategies for non-sterile pharmaceutical manufacturing, including environmental monitoring, water system oversight, microbial limits testing, and regulatory expectations from FDA and USP <1111>.

Ideal for professionals in quality, microbiology, manufacturing, and regulatory compliance.

Course Launch: 24 April 2026

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$840.00

$1,050.00

Computerised Systems & Artificial Intelligence (AI) in GMP

A practical regulatory course covering AI, computerized systems, and upcoming GMP updates including FDA / EMA guidance, Annex 11, and the new Annex 22.

Designed for pharmaceutical professionals who need to understand AI governance, data integrity, digital systems validation, and regulatory expectations for AI adoption in GMP environments.

Course Launch: 24 April 2026

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$840.00

$1,050.00

Risk Management in Medical Devices (ISO 14971)

Master practical risk management for medical devices.

This intensive live course teaches professionals how to implement ISO 14971:2019 risk management processes, maintain compliant Risk Management Files, and align development activities with EU MDR and global regulatory expectations.

Ideal for R&D, QA, Regulatory Affairs, and medical device development teams.

Course Launch: 24 April 2026

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