In pharmaceuticals, ensuring product safety, efficacy and consistency is critical. Every medication must undergo rigorous scrutiny to meet the highest standards. Pharmaceutical validation processes are the key mechanisms that uphold these standards and without them, companies risk compromisin…
The pharmaceutical and biotech industries have one thing in common: a relentless commitment to safety and quality. Maintaining GMP compliance is a regulatory requirement and a moral obligation to ensure the safety and efficacy of your products. Yet, despite its importance, many companies stru…
In comparison with the Federal Decree-Law n8 of 2019, distribution reporting is being reinforced, with notable expansions of scopes, responsibilities and introduction of strict timelines. A national database for reporting counterfeit has been also introduced in an effort to fight such illegal…
Everyone working within the industry must accept the need for a structured and documented change management process. They must first realise the benefits of having a defined change control process, to be able to effectively manage changes that impact on the medicinal products. This is a mindset …
To ensure quality, safety and regulatory compliance, pharmaceutical and biotech companies need to adhere to GMP standards. Structured procedures are maintained with the help of a GMP compliance audit checklist. It guarantees that no important requirement is missed, maintaining operations…
Meeting Good Manufacturing Practice (GMP) standards is essential for trust and reliability, as non-compliance risks product recalls, reputational damage and harm to health. A skilled local GMP auditor ensures effective guidance for your compliance needs.
Let’s unpack what makes regiona…
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