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Computerised system validation is indispensable for Life Sciences organisations, extending beyond mere documentation. This process can be time-consuming without a clear understanding of the system's specific requirements. We focus solely on the essential aspects of validation to ensure compliance with relevant regulations.
Read more...Infrastructure Qualification: Vital for managing applications and systems in the Life Sciences industry, ensuring compliance with regulatory standards and customer expectations. Backed by a team with extensive experience, we specialise in infrastructure qualification for the Life Sciences sector, ensuring adherence to regulatory requirements and industry standards.
Read more...QVAL Consulting, a prominent name in the pharmaceutical sector, excels in implementing risk-based approaches for Computer System Validation and Computer Software Assurance. With our expertise, we ensure the seamless integration of software solutions tailored to the unique needs of the industry. Our commitment to excellence drives us to deliver reliable and compliant systems that meet regulatory standards and industry best practices.
Read more...At QVAL, we offer comprehensive quality management services to support your organisation's regulatory compliance and operational excellence. Our expertise encompasses the implementation of 21 CFR Part 11 and EU Annex 11 controls, ensuring the integrity and security of your electronic records and signatures. We also specialise in the qualification of network and infrastructure and SOP’s.
Read more...QVAL CONSULTING, commonly known as QVAL, is a prominent Pharmaceutical Validation Consulting firm based in Bengaluru, India. Our primary goal is to support Pharma and IT organisations in establishing and maintaining compliance, discovering value in various domains, generating actionable insights, and motivating teams for sustained success. We are dedicated to prioritising the best interests of our clients, team members, and communities, even in the face of obstacles.
With over two decades of experience in life cycle implementation of Computerised Systems, Data integrity Gap Analysis and Remediation, 21 CFR Part 11, Eudralex Annex 11 Compliance, Training programs on CSV, and Audit Readiness for IT Systems, we extend a comprehensive spectrum of independent consulting services to our esteemed clientele.
Over the years, we have rapidly expanded our reach and garnered a diverse client base, both locally and internationally. Our proficiency in the field, coupled with firsthand experience in regulatory agencies and various organisations, enables us to offer project-based and advisory services tailored to meet your consulting needs in India and beyond.
Seasoned professionals with extensive experience in pharmaceutical validation consulting.
Wide range of services covering compliance, value identification, insights development, and team empowerment.
Dedication to always prioritise clients, team members, and communities, ensuring the right actions are taken, even in challenging situations.