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Pharmaceutical/manufacturing compliance with EU and global regulations is of the utmost importance for companies in the pharmaceutical and life sciences industries.

With the lives of the end-user at stake, safety, security, traceability and compliance with stringent standards and ever-evolving regulations is imperative.

“Good Distribution Practice (GDP) is that part of quality assurance which ensures that [medicinal] products are consistently stored, transported and handled under suitable condition as required by the marketing authorisation (MA) or product specification and that traceability is ensured.”

– Health Products Regulatory Authority (HPRA)

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