Optimal’s Quality Assurance Service provides Qualified Person, QP, support for the Chemical and Pharmaceuticals industries, ensuring full regulatory compliance and the safe authorisation of product release. Our QP team offers the specialist knowledge and oversight required to fulfil legally defined QP responsibilities, as outlined by global regulatory authorities. We work in close partnership with your quality assurance and regulatory teams to confirm that batch release processes, product quality reviews and regulatory submissions meet all applicable legal, GMP and compliance requirements. Our consultants provide technical expertise, structured risk assessment and clear decision-making support, maintaining product quality and regulatory alignment across the entire supply chain.
In the Pharmaceuticals industry, where QPs carry significant responsibility for product safety and regulatory adherence, Optimal delivers dependable and highly detailed support. Our consultants perform thorough assessments of batch documentation, quality control data and manufacturing processes to verify compliance with GMP and other regulatory standards. We also provide independent oversight of batch release decisions, ensuring that every product meets specification and satisfies regulatory expectations before it enters the market.
By partnering with Optimal for QP support, organisations can streamline batch release activities, reduce operational and compliance risks, and maintain consistent confidence in the quality of products produced at every stage of the manufacturing process.
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