Mission: To enhance regulatory compliance and customer efficiency by providing innovative GxP solutions
Vision: We strive to be the partner of choice for companies developing cures that enhance human health
Values: Providing exceptional results on time and within budget while acting with integrity.
Pharmatek offer a full range of GxP auditing services in GCP, GLP, GVP cGMP and CSV compliance to the pharmaceutical, medical device and biotechnology industries.
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Our team consists of highly qualified and trained subject matter experts and offers GxP consulting services in GCP, GLP, GVP, cGMP and CSV from development through commercialization.
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Our Inspection Readiness consulting support helps sponsors and CROs to develop quality through proactive risk management and will reduce the concerns and helps towards a successful Inspection outcome.
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Pharmatek SMEs assist in the design, development and implementation of the robust QMS to ensure all regulatory requirements are fulfils and efficient operation of the organization.
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Computer systems validation (CSV) is an essential requirement in the life science industries. Our team of professional CSV auditors, have in depth experience of conducting CSV audits.
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SQA has evolved significantly in response to the changing technological environment. Our software testing services are intensely end-user and performance oriented.
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Pharmatek offers a risk-based approach to the computer system validation process ensuring the right amount of testing and documentation is deployed.
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Pharmatek provides IT infrastructure support Service with care, modernizing platforms and technologies for enhanced agility and scalability with top infrastructure managed services.
